G. Attardi

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Organization and expression of the mammalian mitochondrial genome: a lesson in economy☆

G. Attardi, 1981 .

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation.

M. King, G. Attardi, 1989, Science.

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication.

N. Bresolin, G. Scarlato, G. Attardi, 1999, Science.

The putative mRNA for subunit II of human cytochrome c oxidase starts directly at the translation initiator codon

J. Montoya, G. Attardi, D. Ojala, 1980, Nature.

Isolation of human cell lines lacking mitochondrial DNA.

M. King, G. Attardi, 1996, Methods in enzymology.

Molecular and genetic approaches to the analysis of the informational content of the mitochondrial genome in mammalian cells

G. Attardi, P. Costantino, D. Ojala, 1977, Molecular and Cellular Biochemistry.

Structure and synthesis of ribosomal RNA.

F. Amaldi, G. Attardi, 1970, Annual review of biochemistry.

Size distribution of poly(A)-containing messenger RNA from free polysomes of HeLa cells.

G. Attardi, W. Murphy, 1977, Biochemical and biophysical research communications.

Morphological heterogeneity of HeLa cell mitochondria visualized by a modified diaminobenzidine staining technique.

J. England, G. Attardi, J. Posakony, 1975, Journal of cell science.

Production of Messenger RNA and Regulation of Protein Synthesis

F. Jacob, F. Gros, G. Attardi, 1963 .

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems.

G. Attardi, M. Yoneda, A. Chomyn, 1995, Biochimica et biophysica acta.

Nuclear control of cloverleaf structure of human mitochondrial tRNA(Lys).

M. Helm, G. Attardi, 2004, Journal of molecular biology.

Use of polarography to detect respiration defects in cell cultures.

G. Hofhaus, G. Attardi, R. Shakeley, 1996, Methods in enzymology.

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity.

G. Attardi, M. Guan, N. Fischel‐Ghodsian, 2000, Human molecular genetics.

Regulation of mitochondrial gene expression in mammalian cells.

M. King, P. Polosa, G. Attardi, 1990, Biochemical Society transactions.

Lack of assembly of mitochondrial DNA‐encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene product.

G. Hofhaus, G. Attardi, 1993, The EMBO journal.

Mechanism of mRNA binding to bovine mitochondrial ribosomes.

G. Michaels, J. Montoya, T. W. O'brien, 1989, The Journal of biological chemistry.

Synthesis of chicken hemoglobins during erythrocyte differentiation.

D. Kabat, G. Attardi, 1967, Biochimica et biophysica acta.

ON THE BIOLOGY OF CELLS MODIFIED BY VIRUSES OR ANTIGENS

M. Cohn, G. Attardi, E. Lennox, 2022 .

Novel submicroscopic extrachromosomal elements containing amplified genes in human cells

L. Hood, B. Hamkalo, E. Lai, 1987, Nature.

The biogenesis of mitochondria.

G. Attardi, G. Schatz, G. Schatz, 1970, The Biochemical journal.

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

A. Martinuzzi, G. Attardi, O. Hurko, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Mitochondrial Ribosomes in HeLa Cells

G. Attardi, D. Ojala, 1971 .

Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers.

N. Bresolin, G. Scarlato, G. Attardi, 1994, American journal of human genetics.

Seven unidentified reading frames of human mitochondrial DNA encode subunits of the respiratory chain NADH dehydrogenase.

R. Doolittle, P. Mariottini, C. Ragan, 1986, Cold Spring Harbor symposia on quantitative biology.

The nucleotide sequence of the cDNA coding for the human dihydrofolic acid reductase.

G. Attardi, J. Masters, 1983, Gene.

Association of a protein structure of probable membrane derivation with HeLa cell mitochondrial DNA near its origin of replication.

J. Griffith, G. Attardi, M. Albring, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Human dihydrofolate reductase gene organization. Extensive conservation of the G + C-rich 5' non-coding sequence and strong intron size divergence from homologous mammalian genes.

G. Attardi, J. Masters, J. Yang, 1984, Journal of molecular biology.

High molecular weight nonribosomal-type nuclear RNA and cytoplasmic messenger RNA in HeLa cells.

G. Attardi, J. Houssais, 1966, Proceedings of the National Academy of Sciences of the United States of America.

Fate of mitochondrial DNA in human-mouse somatic cell hybrids (density gradient centrifugation-ethidium bromide-karyotype).

G. Attardi, B. Attardi, 1972, Proceedings of the National Academy of Sciences of the United States of America.

Discrete human dihydrofolate reductase gene transcripts present in polysomal RNA map with their 5' ends several hundred nucleotides upstream of the main mRNA start site

G. Attardi, J. Masters, 1985, Molecular and cellular biology.

Molecular characterization of the transcription termination factor from human mitochondria.

R. Aebersold, D. Hess, V. Micol, 1993, The Journal of biological chemistry.

A comparison of the primary structures of 28S and 18S ribonucleic acid from HeLa cells and different human tissues.

F. Amaldi, G. Attardi, 1971, Biochemistry.

Membrane-bound ribosomes in HeLa cells. I. Their proportion to total cell ribosomes and their association with messenger RNA.

G. Attardi, B. Attardi, B. Cravioto, 1969, Journal of molecular biology.

Partial sequence analysis of ribosomal RNA from HeLa cells. I. Oligonucleotide pattern of 28 s and 18 s RNA after pancreatic ribonuclease digestion.

F. Amaldi, G. Attardi, 1968, Journal of molecular biology.

Partial sequence analysis of ribosomal RNA from HeLa cells. II. Evidence for sequences of non-ribosmal type in 45 and 32 s ribosomal RNA precursors.

F. Amaldi, P. Jeanteur, G. Attardi, 1968, Journal of molecular biology.

A new type of EcoRI polymorphism of the human ribosomal DNA repeating unit revealed by analysis of cloned DNA fragments.

J. Montoya, G. Attardi, M. Mottes, 1984, Gene.

A human dihydrofolate reductase pseudogene and its relationship to the multiple forms of specific messenger RNA.

G. Attardi, J. Masters, J. Yang, 1983, Journal of molecular biology.

Oligonucleotide pattern after pancreatic ribonuclease digestion and the 3' and 5' termini of 5S ribonucleic acid from HeLa cells.

F. Amaldi, G. Attardi, L. Hatlen, 1969, Biochemistry.

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

G. Attardi, M. Yoneda, T. Miyatake, 1994, Molecular and cellular biology.

Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable

G. Attardi, R. Gelfand, G. Attardi, 1981, Molecular and cellular biology.

A Comprehensive View of Mitochondrial Gene Expression in Human Cells

J. Montoya, S. Crews, G. Attardi, 1982 .

Virus specific protein and a ribo-nucleic acid associated with ribosomes in poliovirus infected HeLa cells.

G. Attardi, J. Smith, 1962, Cold Spring Harbor symposia on quantitative biology.

Analysis of sequence homology between human and mouse mitochondrial DNA.

G. Attardi, L. de Francesco, 1980, Journal of molecular biology.

Fine mapping of the ribosomal RNA genes of HeLa cell mitochondrial DNA.

G. Attardi, D. Ojala, 1980, Journal of molecular biology.

Photosensitivity and heat resistance conferred by BrdU incorporation upon a thymidine kinase-deficient mouse cell line with persistent mitochondrial enzyme activity.

G. Attardi, C. Tu, B. Keeley, 1975, Journal of cell science.

Isolation, subunit composition, and site of synthesis of human cytochrome c oxidase.

J. Hare, G. Attardi, E. Ching, 1980, Biochemistry.

Expression of the mitochondrial genome in HeLa cells. VI. Size determination of mitochondrial ribosomal RNA by electron microscopy.

G. Attardi, N. Davidson, Y. Aloni, 1971, Journal of molecular biology.

Studies of fractionated HeLa cell metaphase chromosomes. II. chromosomal distribution of sites for transfer RNA and 5 s RNA.

G. Attardi, Y. Aloni, L. Hatlen, 1971, Journal of Molecular Biology.

Relationship between HeLa cell ribosomal RNA and its precursors studied by high resolution RNA-DNA hybridization.

P. Jeanteur, G. Attardi, 1969, Journal of molecular biology.

In vivo measurements of respiration control by cytochrome c oxidase and in situ analysis of oxidative phosphorylation.

G. Attardi, G. Villani, 2001, Methods in cell biology.

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.

G. Attardi, G Attardi, G Villani, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Polarographic assays of respiratory chain complex activity.

G. Attardi, G. Villani, 2007, Methods in cell biology.

Low Reserve of Cytochrome c Oxidase Capacity in Vivo in the Respiratory Chain of a Variety of Human Cell Types*

S. Papa, G. Attardi, M. Greco, 1998, The Journal of Biological Chemistry.

Multiple forms of human dihydrofolate reductase messenger RNA. Cloning and expression in Escherichia coli of their DNA coding sequence.

C. Morandi, G. Attardi, M. Mottes, 1982, Journal of molecular biology.

Specific requirement for ATP at an early step of in vitro transcription of human mitochondrial DNA.

G. Attardi, N. Narasimhan, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Identification of initiation sites for heavy-strand and light-strand transcription in human mitochondrial DNA.

M. Rabinowitz, David Levens, J. Montoya, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Fractionation of mitochondrial RNA from HeLa cells by high-resolution electrophoresis under strongly denaturing conditions.

F. Amalric, G. Attardi, R. Gelfand, 1978, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. X. Properties of mitochondrial polysomes.

G. Attardi, D. Ojala, 1972, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells: I. Properties of the discrete RNA components from the mitochondrial fraction☆

G. Attardi, B. Attardi, G. Attardi, 1971 .

Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria

R. Doolittle, P. Mariottini, G. Attardi, 1983, Cell.

Sedimentation Properties of RNA Species homologous to Mitochondrial DMA in HeLa Cells

G. Attardi, B. Attardi, 1969, Nature.

Distinctive pattern and translational control of mitochondrial protein synthesis in rat brain synaptic endings.

P. Polosa, G. Attardi, P. L. Polosa, 1991, The Journal of biological chemistry.

Recognition of ribosomal RNA sites in DNA. I. Analysis of the E. coli system.

P. C. Huang, G. Attardi, S. Kabat, 1965, Proceedings of the National Academy of Sciences of the United States of America.

Strikingly higher frequency in centenarians and twins of mtDNA mutation causing remodeling of replication origin in leukocytes

J. Fish, C. Franceschi, M. Bonafè, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Reversible tenfod reduction in mitochondrial DNA content of human cells treated with ethidium bromide

G. Attardi, A. Wiseman, 1978, Molecular and General Genetics MGG.

Brief Communication: Role of Nuclear Background and in vivo Environment in Variable Segregation Behavior of the Aging-Dependent T414G Mutation at Critical Control Site for Human Fibroblast mtDNA Replication

G. Attardi, Y. Michikawa, K. Richter, 1999, Somatic cell and molecular genetics.

Identification and partial characterization of multiple discrete polyadenylic acid containing RNA components coded for by HeLa cell mitochondrial DNA.

G. Attardi, D. Ojala, G. Attardi, 1974, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. XIX. Occurrence in mitochondria of polyadenylic acid sequences, "free" and covalently linked to mitochondrial DNA-coded RNA.

G. Attardi, D. Ojala, 1974, Journal of molecular biology.

MOLECULAR APPROACHES TO THE DISSECTION OF THE MITOCHONDRIAL GENOME IN HELA CELLS

G. Attardi, D. Ojala, Paolo Constantino, 1974 .

Proteolytic Processing of OPA1 Links Mitochondrial Dysfunction to Alterations in Mitochondrial Morphology*

S. Duvezin-Caubet, R. Jagasia, A. Reichert, 2006, Journal of Biological Chemistry.

The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units

J. Montoya, G. Attardi, G. Gaines, 1983, Cell.

Heteroplasmic mitochondrial tRNALys mutation and its complementation in MERRF patient‐derived mitochondrial transformants

T. Miyatake, G. Attardi, M. Yoneda, 1995, Muscle & nerve. Supplement.

Photolabelling of a mitochondrially encoded subunit of NADH dehydrogenase with [3H]dihydrorotenone

C. Ragan, G. Attardi, Salil D. Patel, 1987, FEBS letters.

Two distinct genes for ADP/ATP translocase are expressed at the mRNA level in adult human liver.

J. Houldsworth, G. Attardi, 1988, Proceedings of the National Academy of Sciences of the United States of America.

tRNA punctuation model of RNA processing in human mitochondria

Julio Montoya, J. Montoya, G. Attardi, 1981, Nature.

Atypical pattern of utilization of amino acids for mitochondrial protein synthesis in HeLa cells.

G. Attardi, P. Costantino, 1973, Proceedings of the National Academy of Sciences of the United States of America.

The RNase P Associated with HeLa Cell Mitochondria Contains an Essential RNA Component Identical in Sequence to That of the Nuclear RNase P

G. Attardi, R. S. Puranam, 2001, Molecular and Cellular Biology.

The mtDNA‐encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme

G. Attardi, Yidong Bai, 1998, The EMBO journal.

Mitochondrial Gene Products

G. Attardi, A. Chomyn, 1987 .

Nucleotide sequence of a fragment of HeLa-cell mitochondrial DNA containing the precisely localized origin of replication.

S. Crews, G. Attardi, D. Ojala, 1979, Cold Spring Harbor symposia on quantitative biology.

Uniparental propagation of mitochondrial DNA in mouse-human cell hybrids.

C. Croce, G. Attardi, L. de Francesco, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Identification of discrete electrophoretic components among the products of mitochondrial protein synthesis in HeLa cells.

G. Attardi, P. Costantino, 1975, Journal of molecular biology.

Mitochondrial origin of membrane-associated heterogeneous RNA in HeLa cells.

G. Attardi, B. Attardi, 1968, Proceedings of the National Academy of Sciences of the United States of America.

Expression of the mitochondrial genome in HeLa cells. XIV. The relative positions of the 4 S RNA genes and of the ribosomal RNA genes in mitochondrial DNA.

M. Wu, N. Davidson, G. Attardi, 1972, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells: IV. Titration of mitochondrial genes for 16 s, 12 s and 4 s RNA☆☆☆

G. Attardi, Y. Aloni, 1971 .

Cytoplasmic transfer of chloramphenicol resistance in a human cell line

G. Attardi, C. Mitchell, Giuseppe Attardi, 1978, Somatic cell genetics.

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

R. Doolittle, P. Mariottini, C. Ragan, 1985, Nature.

Expression of the mitochondrial genome in HeLa cells. 13. Effect of selective inhibition of cytoplasmic or mitochondrial protein synthesis on mitochondrial nucleic acid synthesis.

B. Storrie, G. Attardi, 1972, Journal of molecular biology.

Selective in vivo damage by "visible" light of BrdU-containing mitochondrial DNA in a thymidine kinase-deficient mouse cell line with persistent mitochondrial enzyme activity.

G. Attardi, B. Croizat, 1975, Journal of cell science.

Identification of discrete polyadenylate-containing RNA components transcribed from HeLa cell mitochondrial DNA.

G. Attardi, D. Ojala, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Giant-size rapidly labeled nuclear ribonucleic acid and cytoplasmic messenger ribonucleic acid in immature duck erythrocytes.

H. Parnas, G. Attardi, B. Attardi, 1966, Journal of molecular biology.

Persistence of thymidine kinase activity in mitochondria of a thymidine kinase-deficient derivative of mouse L cells.

G. Attardi, B. Attardi, 1972, Proceedings of the National Academy of Sciences of the United States of America.

Mitochondrial growth and division during the cell cycle in HeLa cells

J. England, G. Attardi, JW Posakony, 1977, The Journal of cell biology.

A membrane-associated RNA of cytoplasmic origin in HeLa cells.

G. Attardi, B. Attardi, 1967, Proceedings of the National Academy of Sciences of the United States of America.

Expression of the mitochondrial genome in HeLa cells: IX. Replication of mitochondrial DNA in relationship to the cell cycle in HeLa cells

G. Attardi, L. Pica-Mattoccia, G. Attardi, 1972 .

EXPRESSION OF THE MITOCHONDRIAL GENOME IN HELA CELLS

B. Storrie, G. Attardi, 1973, The Journal of cell biology.

THE ORGANIZATION OF THE GENES IN THE HUMAN MITOCHONDRIAL GENOME AND THEIR MODE OF TRANSCRIPTION

S. Crews, G. Attardi, P. Cantatore, 1979 .

Cytoplasmically determined human cell mutants defective in mitochondrial ribosome assembly

G. Attardi, A. Wiseman, 2004, Molecular and General Genetics MGG.

Tight Control of Respiration by NADH Dehydrogenase ND5 Subunit Gene Expression in Mouse Mitochondria

G. Attardi, Yidong Bai, R. Shakeley, 2000, Molecular and Cellular Biology.

Expression in Mouse Mitochondria Dehydrogenase ND 5 Subunit Gene Tight Control of Respiration by NADH

G. Attardi, Yidong Bai, R. Shakeley, 1999 .

Respiration and Growth Defects in Transmitochondrial Cell Lines Carrying the 11778 Mutation Associated with Leber's Hereditary Optic Neuropathy*

G. Hofhaus, G. Attardi, O. Hurko, 1996, The Journal of Biological Chemistry.

Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

G. Hofhaus, G. Attardi, 1995, Molecular and cellular biology.

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.

N. Bresolin, G. Meola, G. Scarlato, 1991, Molecular and cellular biology.

Cytoplasmically inherited mutations of a human cell line resulting in deficient mitochondrial protein synthesis

G. Attardi, A. Wiseman, Giuseppe Attardi, 1979, Somatic cell genetics.

Biogenesis of mitochondrial proteins in HeLa cells.

G. Attardi, E. Ching, 1979, Methods in enzymology.

Biochemical and electron microscopic characterization of DNA-RNA complexes from HeLa cell mitochondria.

G. Attardi, D. Carré, 1978, Biochemistry.

Mitochondrial RNA and protein synthesis in enucleated African green monkey cells.

J. England, G. Attardi, P. Costantino, 1978, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. XXI. Mitochondrial protein synthesis during the cell cycle.

J. England, G. Attardi, 1974, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. XVI. Electrophoretic properties of the products of in vivo and in vitro mitochondrial protein synthesis.

G. Attardi, M. Lederman, 1973, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. XI. Isolation and characterization of transcription complexes of mitochondrial DNA.

G. Attardi, Y. Aloni, 1972, Journal of molecular biology.

Expression of the mitochondrial genome in HeLa cells. V. Transcription of mitochondrial DNA in relationship to the cell cycle.

G. Attardi, L. Pica-Mattoccia, 1971, Journal of molecular biology.

In vitro protein synthesis in a mitochondrial fraction from HeLa cells: sensitivity to antibiotic and ethidium bromide.

G. Attardi, M. Lederman, 1970, Biochemical and biophysical research communications.

Distribution of repetitive and nonrepetivite sequence transcripts in HeLa mRNA.

R. Britten, E. Davidson, W. Klein, 1974, Proceedings of the National Academy of Sciences of the United States of America.

Human dihydrofolate reductase gene is located in chromosome 5 and is unlinked to the related pseudogenes.

F. Ruddle, P. Barker, G. Attardi, 1984, Proceedings of the National Academy of Sciences of the United States of America.

Isolation and characterization of dihydrofolic acid reductase from methotrexate-sensitive and -resistant human cell lines.

C. Morandi, G. Attardi, 1981, The Journal of biological chemistry.

Methylation of nucleic acids in HeLa cells.

G. Brown, G. Attardi, 1965, Biochemical and biophysical research communications.

URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit.

R. Doolittle, C. Ragan, M. Riley, 1986, Science.

Animal mitochondrial DNA: an extreme example of genetic economy.

G. Attardi, 1985, International review of cytology.

High-resolution electrophoretic fractionation and partial characterization of the mitochondrial translation products from HeLa cells.

G. Attardi, E. Ching, 1982, Biochemistry.

Termination of transcription in human mitochondria: Identification and purification of a DNA binding protein factor that promotes termination

G. Attardi, B. Kruse, N. Narasimhan, 1989, Cell.

Characterization of an RNase P activity from HeLa cell mitochondria. Comparison with the cytosol RNase P activity.

S. Altman, C. Guerrier-Takada, G. Attardi, 1985, The Journal of biological chemistry.

Proportion of HeLa cell genome complementary to transfer RNA and 5 s RNA.

G. Attardi, L. Hatlen, 1971, Journal of molecular biology.

ANALYSIS OF RNA SYNTHESIZED BY AN ISOLATED RAT BRAIN SYNAPTOSOMAL FRACTION

J. M. England, G. Attardi, 1976, Journal of neurochemistry.

Amino acid specificity of the transfer RNA species coded for by HeLa cell mitochondrial DNA.

G. Attardi, D. Lynch, 1976, Journal of molecular biology.

Identification of the polypeptides encoded in the ATPase 6 gene and in the unassigned reading frames 1 and 3 of human mtDNA.

R. Doolittle, P. Mariottini, M. Riley, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Distinctive features of the 5′-terminal sequences of the human mitochondrial mRNAs

J. Montoya, G. Attardi, D. Ojala, 1981, Nature.

The tRNA genes punctuate the reading of genetic information in human mitochondrial DNA

G. Attardi, D. Ojala, R. Gelfand, 1980, Cell.

The sequences of the small ribosomal RNA gene and the phenylalanine tRNA gene are joined end to end in human mitochondrial DNA

S. Crews, G. Attardi, 1980, Cell.

Stability of cytoplasmic messenger RNA in HeLa cels.

G. Attardi, W. Murphy, 1973, Proceedings of the National Academy of Sciences of the United States of America.

Transcription of Mitochondrial DNA in HeLa Cells

B. Storrie, G. Attardi, B. Attardi, 1970 .

Early appearance and long-term persistence of the submicroscopic extrachromosomal elements (amplisomes) containing the amplified DHFR genes in human cell lines.

G. Pauletti, E. Lai, G. Attardi, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Highly efficient RNA-synthesizing system that uses isolated human mitochondria: new initiation events and in vivo-like processing patterns

G. Attardi, G. Gaines, 1984, Molecular and cellular biology.

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA

Michael P. King, M. King, G. Attardi, 1988, Cell.

In vivo control of respiration by cytochrome c oxidase in human cells.

G. Attardi, G Attardi, G Villani, 2000, Free radical biology & medicine.

Functional Analysis of in Vivo and in Organello Footprinting of HeLa Cell Mitochondrial DNA in Relationship to ATP and Ethidium Bromide Effects on Transcription*

P. Fernández-Silva, V. Micol, G. Attardi, 1997, The Journal of Biological Chemistry.

The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions

P. Fernández-Silva, F. Martínez-Azorín, V. Micol, 1997, The EMBO journal.

Analysis of aminoacylation of human mitochondrial tRNAs.

J. Enríquez, G. Attardi, JoséAntonio Enríquez, 1996, Methods in enzymology.

Markedly different ATP requirements for rRNA synthesis and mtDNA light strand transcription versus mRNA synthesis in isolated human mitochondria.

G. Attardi, G. Gaines, C. Rossi, 1987, The Journal of biological chemistry.

MtDNA mutations in aging and apoptosis.

G. Attardi, A. Chomyn, 2003, Biochemical and biophysical research communications.

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation.

G. Attardi, M. Guan, N. Fischel‐Ghodsian, 1996, Human molecular genetics.

Very Rare Complementation between Mitochondria Carrying Different Mitochondrial DNA Mutations Points to Intrinsic Genetic Autonomy of the Organelles in Cultured Human Cells*

J. Enríquez, M. Bayona-Bafaluy, G. Attardi, 2000, The Journal of Biological Chemistry.

[28] Mitochondria-mediated transformation of human ϱ0 cells

M. King, G. Attardi, 1996 .

The Deafness-Associated Mitochondrial DNA Mutation at Position 7445, Which Affects tRNASer(UCN) Precursor Processing, Has Long-Range Effects on NADH Dehydrogenase Subunit ND6 Gene Expression

J. Enríquez, G. Attardi, R. S. Puranam, 1998, Molecular and Cellular Biology.

Expression of the mitochondrial genome in HeLa cells. XII. Relationship between mitochondrial fast-sedimenting RNA components and ribosomal and 4 s RNA.

G. Attardi, Y. Aloni, 1972, Journal of molecular biology.

Symmetrical in vivo transcription of mitochondrial DNA in HeLa cells.

G. Attardi, Y. Aloni, 1971, Proceedings of the National Academy of Sciences of the United States of America.

Comprehensive, rapid and sensitive detection of sequence variants of human mitochondrial tRNA genes.

G. Hofhaus, L. Lerman, G. Attardi, 1997, Nucleic acids research.

Mapping of nascent light and heavy strand transcripts on the physical map of HeLa cell mitochondrial DNA.

G. Attardi, P. Cantatore, 1980, Nucleic acids research.

Molecular and biological characterization of messenger RNA.

H. Hiatt, W. Gilbert, J. Watson, 1961, Cold Spring Harbor symposia on quantitative biology.

Pattern of RNA synthesis in duck erythrocytes in relationship to the stage of cell differentiation.

H. Parnas, G. Attardi, B. Attardi, 1970, Experimental cell research.

Detection and quantification of point mutations in mitochondrial DNA by PCR.

S. Tsuji, G. Attardi, M. Yoneda, 1996, Methods in enzymology.

Genetic and Functional Analysis of Mitochondrial DNA‐Encoded Complex I Genes

T. Yagi, G. Attardi, Yidong Bai, 2004, Annals of the New York Academy of Sciences.

STIMULATION OF THE RATE OF SYNTHESIS OF SPECIFIC MESSENGER RNA AFTER ENZYME INDUCTION IN E. COLI

G. Attardi, 1963 .

Mitochondrial biogenesis and genetics

G. Attardi, A. Chomyn, 1995 .

Role of mitochondrial DNA in human aging.

G. Attardi, 2002, Mitochondrion.

Muscle-specific mutations accumulate with aging in critical human mtDNA control sites for replication

K. Yarasheski, S. Bhasin, W. Engel, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Discovery of a Major D-Loop Replication Origin Reveals Two Modes of Human mtDNA Synthesis

J. Fish, G. Attardi, N. Raule, 2004, Science.

A small polyadenylated RNA (7 S RNA), containing a putative ribosome attachment site, maps near the origin of human mitochondrial DNA replication.

J. Montoya, S. Crews, G. Attardi, 1981, Journal of molecular biology.

Search for differences in post-transcriptional modification patterns of mitochondrial DNA-encoded wild-type and mutant human tRNALys and tRNALeu(UUR).

C. Florentz, M. Helm, G. Attardi, 1999, Nucleic acids research.

Relationship of genotype to phenotype in fibroblast-derived transmitochondrial cell lines carrying the 3243 mutation associated with the MELAS encephalomyopathy: shift towards mutant genotype and role of mtDNA copy number.

G. Attardi, H. Bentlage, H.A.C.M. Bentlage, 1996, Human molecular genetics.

Characterization of double-stranded RNA from HeLa cell mitochondria.

G. Attardi, P. Young, 1975, Biochemical and biophysical research communications.

Precise localization of the origin of replication in a physical map of HeLa cell mitochondrial DNA and isolation of a small fragment that contains it.

G. Attardi, D. Ojala, 1978, Journal of Molecular Biology.

A detailed physical map of HeLa cell mitochondria DNA and its alignment with the positions of known genetic markers.

G. Attardi, D. Ojala, 1977, Plasmid.

Expression of the mitochondrial genome in HeLa cells: VIII. The relative position of ribosomal RNA genes in mitochondrial DNA☆☆☆

G. Attardi, N. Davidson, Y. Aloni, 1972 .

An electron microscope study of the relative positions of the 4S and ribosomal RNA genes in HeLa cell mitochondrial DNA

N. Davidson, L. Angerer, G. Attardi, 1976, Cell.

Expression of the mitochondria genome in HeLa cells. IV. Titration of mitochondrial genes for 16 s, 12 s and 4 s RNA.

G. Attardi, Y. Aloni, 1971, Journal of molecular biology.

Electron microscopic visualization of mitochondrial RNA-DNA hybrids.

G. Attardi, Y. Aloni, D. Robberson, 1971, Journal of molecular biology.

Nucleotide sequence of a region of human mitochondrial DNA containing the precisely identified origin of replication

J. Posakony, S. Crews, G. Attardi, 1979, Nature.

The mechanism of protein synthesis.

G. Attardi, 1967, Annual review of microbiology.

Aging-dependent Functional Alterations of Mitochondrial DNA (mtDNA) from Human Fibroblasts Transferred into mtDNA-less Cells*

N. Bresolin, G. Scarlato, G. Attardi, 1996, The Journal of Biological Chemistry.

Isolation and assay of mitochondrial transcription termination factor from human cells.

P. Fernández-Silva, V. Micol, G. Attardi, 1996, Methods in enzymology.

Symposium on the biology of cells modified by viruses or antigens. II. On the analysis of antibody synthesis at the cellular level.

M. Cohn, G. Attardi, E. Lennox, 1959, Bacteriological reviews.

Termination Factor-Mediated DNA Loop between Termination and Initiation Sites Drives Mitochondrial rRNA Synthesis

J. Griffith, Anthony J. Cesare, Jae-Hyoung Cho, 2005, Cell.

Functional and morphological abnormalities of mitochondria harbouring the tRNALeu(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease

J. Maassen, C. Wollheim, J. V. D. van den Ouweland, 1999, Diabetologia.

The Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episode Syndrome-associated Human Mitochondrial tRNALeu(UUR) Mutation Causes Aminoacylation Deficiency and Concomitant Reduced Association of mRNA with Ribosomes*

J. Enríquez, P. Fernández-Silva, V. Micol, 2000, The Journal of Biological Chemistry.

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNALys and premature translation termination

J. Enríquez, G. Attardi, A. Chomyn, 1995, Nature Genetics.

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

I. Nonaka, C. Angelini, A. Martinuzzi, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Identification and mapping of human mitochondrial genes.

J. Montoya, G. Attardi, D. Ojala, 1982, Birth defects original article series.

Mitochondrial Outer Membrane Permeability Change and Hypersensitivity to Digitonin Early in Staurosporine-induced Apoptosis*

Shili Duan, G. Attardi, A. Chomyn, 2003, The Journal of Biological Chemistry.

Chapter 20 Recent advances on mitochondrial biogenesis

G. Attardi, A. Chomyn, 1992 .

ISOLATION OF METAPHASE CHROMOSOMES FROM HELA CELLS

J. Huberman, G. Attardi, 1966, The Journal of cell biology.

Variable content of double minute chromosomes is not correlated with degree of phenotype instability in methotrexate-resistant human cell lines.

H. Gay, G. Attardi, J. Masters, 1982, Molecular and cellular biology.

Identification of a Novel Mitochondrial Complex Containing Mitofusin 2 and Stomatin-like Protein 2*

G. Attardi, Petr Hájek, Anne Chomyn, 2007, Journal of Biological Chemistry.

Heterogeneous Efficiencies of mRNA Translation in Human Mitochondria

G. Attardi, A. Chomyn, 1987 .

Use of a DNA probe for mapping by electron microscopy the ribosomal sequences in ribosomal RNA precursors from duck cells.

G. Attardi, W. Murphy, 1974, Journal of molecular biology.

Electrofocusing analysis of HeLa cell metaphase chromosomes.

G. Attardi, M. Raftery, Y. Aloni, 1972, Biochemistry.

Studies of fractionated HeLa cell metaphase chromosomes: I. The chromosomal distribution of DNA complementary to 28 s and 18 s ribosomal RNA and to cytoplasmic messenger RNA

J. Huberman, G. Attardi, 1967 .

Mitochondrial DNA transcription initiation and termination using mitochondrial lysates from cultured human cells.

P. Fernández-Silva, V. Micol, G. Attardi, 1996, Methods in enzymology.

In vivo footprinting of human mitochondrial DNA in cultured cell systems.

P. Fernández-Silva, V. Micol, G. Attardi, 1996, Methods in enzymology.

In situ photochemical crosslinking of HeLa cell mitochondrial DNA by a psoralen derivative reveals a protected region near the origin of replication.

L. Defrancesco, G. Attardi, 1981, Nucleic acids research.

The site of synthesis of the iron-sulfur subunits of the flavoprotein and iron-protein fractions of human NADH dehydrogenase.

C. Ragan, G. Attardi, A. Chomyn, 1988, The Journal of biological chemistry.

The elucidation of the human mitochondrial genome: a historical perspective.

G. Attardi, 1986, BioEssays : news and reviews in molecular, cellular and developmental biology.

Behavior in Vitro of Normal and Neoplastic Melanocytes of the Human Choroid

G. Attardi, F. Moro, 1959 .

Multiple deficiencies of mitochondrial DNA- and nuclear-encoded subunits of respiratory NADH dehydrogenase detected with peptide- and subunit-specific antibodies in mitochondrial myopathies.

J. Walker, H. Schägger, R. Sengers, 1995, Biochimica et biophysica acta.

Functions of the Proteins Encoded in Human Mitochondrial DNA

P. Mariottini, G. Attardi, A. Chomyn, 1987 .

Lack of Complex I Activity in Human Cells Carrying a Mutation in MtDNA-encoded ND4 Subunit Is Corrected by theSaccharomyces cerevisiae NADH-Quinone Oxidoreductase (NDI1) Gene*

A. Matsuno-Yagi, T. Yagi, G. Attardi, 2001, The Journal of Biological Chemistry.

Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant

Daniel T. Knoepfle, S. Benzer, D. Walker, 2006, Proceedings of the National Academy of Sciences.

Impaired ATP Synthase Assembly Associated with a Mutation in the Human ATP Synthase Subunit 6 Gene*

N. Henderson, L. Nijtmans, G. Attardi, 2001, The Journal of Biological Chemistry.

Antibodies against the COOH-terminal undecapeptide of subunit II, but not those against the NH2-terminal decapeptide, immunoprecipitate the whole human cytochrome c oxidase complex.

R. Doolittle, P. Mariottini, G. Attardi, 1986, The Journal of biological chemistry.

Failure to detect "cap" structures in mitochondrial DNA-coded poly(A)-containing RNA from HeLa cells.

S. Crews, K. Grohmann, G. Attardi, 1978, Nucleic acids research.

The multiple ADP/ATP translocase genes are differentially expressed during human muscle development.

W. Engel, G. Attardi, O. Hurko, 1992, The Journal of biological chemistry.

Alignment of the amino terminal amino acid sequence of human cytochrome c oxidase subunits I and II with the sequence of their putative mRNAs.

M. Hunkapiller, G. Attardi, A. Chomyn, 1981, Nucleic acids research.

Flux control of cytochrome c oxidase in human skeletal muscle.

C. Elger, W. Kunz, S. Vielhaber, 2000, The Journal of biological chemistry.

cDNA-derived amino acid sequence of the NADH-binding 51-kDa subunit of the bovine respiratory NADH dehydrogenase reveals striking similarities to a bacterial NAD(+)-reducing hydrogenase.

R. Aebersold, G. Attardi, S. Patel, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation.

G. Attardi, M. Guan, N. Fischel‐Ghodsian, 2001, Human molecular genetics.

Sequence analysis and precise mapping of the 3' ends of HeLa cell mitochondrial ribosomal RNAs.

J. Montoya, G. Attardi, D. Dubin, 1982, Journal of molecular biology.

Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells.

M. King, G. Attardi, 1993, The Journal of biological chemistry.

Evidence for complete symmetrical transcription in vivo of mitochondrial DNA in HeLa cells.

G. Attardi, B. Attardi, C. Tu, 1975, Journal of molecular biology.

Decreased Reactive Oxygen Species Production in Cells with Mitochondrial Haplogroups Associated with Longevity

G. Attardi, A. Chomyn, Ai Chen, 2012, PloS one.

Isolation of chloramphenicol-resistant variants from a human cell line

G. Attardi, J. England, C. Mitchell, 1975, Somatic cell genetics.

Rate-limiting Step Preceding Cytochrome c Release in Cells Primed for Fas-mediated Apoptosis Revealed by Analysis of Cellular Mosaicism of Respiratory Changes*

G. Attardi, G. Villani, P. Hájek, 2001, The Journal of Biological Chemistry.

Biaffine Dependency and Semantic Graph Parsing for EnhancedUniversal Dependencies

M. Simi, G. Attardi, Daniele Sartiano, 2021, IWPT.

Myoclonic Epilepsy and Ragged Red Fibers (MERRF) Syndrome: Selective Vulnerability of CNS Neurons Does Not Correlate with the Level of Mitochondrial tRNAlys Mutation in Individual Neuronal Isolates

C. Miller, G. Attardi, A. Chomyn, 1997, The Journal of Neuroscience.

ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. II. FURTHER OBSERVATIONS ON THE BEHAVIOR OF SINGLE ANTIBODY-PRODUCING CELLS WITH RESPECT TO THEIR SYNTHETIC CAPACITY AND MORPHOLOGY.

M. Cohn, G. Attardi, E. Lennox, 1964, Journal of immunology.

Antibody Formation by Rabbit Lymph Node Cells

M. Cohn, G. Attardi, E. Lennox, 1964, The Journal of Immunology.

MODE OF MITOCHONDRIAL FORMATION IN HELA CELLS

B. Storrie, G. Attardi, 1973, Journal of Cell Biology.

Assignment of human dihydrofolate reductase gene to band q23 of chromosome 5 and of related pseudogene ΨHD1 to chromosome 3

J. Wasmuth, G. Attardi, B. Maurer, 1985, Somatic cell and molecular genetics.

N. Bresolin, S. Papa, G. Attardi, 2003, The FASEB Journal.

Mitochondrial protein synthesis in HeLa cells.

J. England, B. Storrie, G. Attardi, 1973, Acta endocrinologica. Supplementum.

ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. I. SINGLE CELL RESPONSES TO SEVERAL ANTIGENS.

M. Cohn, G. Attardi, E. Lennox, 1964, Journal of immunology.

Analysis of human mitochondrial RNA.

J. Montoya, G. Attardi, 1983, Methods in enzymology.

[41] Analysis of human mitochondrial RNA

J. Montoya, G. Attardi, 1983 .

A Monomer-to-Trimer Transition of the Human Mitochondrial Transcription Termination Factor (mTERF) Is Associated with a Loss of in Vitro Activity*

M. Helm, G. Attardi, J. Asin-Cayuela, 2004, Journal of Biological Chemistry.

The mutation rate of the human mtDNA deletion mtDNA4977.

S. Tavaré, R. Shenkar, N. Arnheim, 1996, American journal of human genetics.

Metabolic properties of the products of mitochondrial protein synthesis in HeLa cells.

G. Attardi, P. Costantino, 1977, The Journal of biological chemistry.

Demonstration in vivo and in vitro of Peristaltic Contractions in the Portal Vein of Adult Mammals (Rodents)

G. Attardi, 1955, Nature.

Mitochondrial ribssome in HeLa cells.

G. Attardi, D. Ojala, 1971, Nature: New biology.

ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. V. CELLULAR HETEROGENEITY IN THE PRODUCTION OF ANTIBODY TO T5.

M. Cohn, G. Attardi, E. Lennox, 1964, Journal of Immunology.

ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS. IV. THE DETAILED METHODS FOR MEASURING ANTIBODY SYNTHESIS BY INDIVIDUAL CELLS, THE KINETICS OF ANTIBODY FORMATION BY RABBITS AND THE PROPERTIES OF CELL SUSPENSIONS.

M. Cohn, G. Attardi, E. Lennox, 1964, Journal of Immunology.

ANTIBODY FORMATION BY RABBIT LYMPH NODE CELLS.III. THE CONTROLS FOR MICRODROP AND MICROPIPET EXPERIMENTS.

M. Cohn, G. Attardi, E. Lennox, 1964, Journal of immunology.

Amplisomes : Novel Submicroscopic Extrachromosomal Elements Containing Amplified Genes

G. Attardi, 2020 .

Purified and Protein-Loaded Mitochondrial Outer Membrane Vesicles for Functional Analysis of Preprotein Transport

G. Attardi, A. Chomyn, 2018 .

Differential regulation of expression of the multiple ADP/ATP translocase genes in human cells.

G. Attardi, J. Lunardi, 1991, The Journal of biological chemistry.

R. Burk, N. Barzilai, G. Atzmon, 2007, Mitochondrion.

Screening for aging-dependent point mutations in mtDNA.

G. Attardi, Y. Michikawa, 2002, Methods in molecular biology.

Identification of the polypeptides encoded in the unassigned reading frames 2, 4, 4L, and 5 of human mitochondrial DNA.

R. Doolittle, P. Mariottini, B. Cottrell, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Organization and expression of the mammalian mitochondrial genome: a lesson in economy☆

G. Attardi, 1981 .

Transcription system using a HeLa cell mitochondrial lysate.

G. Attardi, B. Kruse, N. N. Murdter, 1995, Methods in molecular biology.

The excised leader of human cytochrome c oxidase subunit I mRNA which contains the origin of mitochondrial DNA light-strand synthesis accumulates in mitochondria and is polyadenylated.

G. Attardi, G. Gaines, C. Rossi, 1987, Molecular and cellular biology.

An ultraviolet microspectrophotometric study of the purkinje cells of the adult albino rat

G. Attardi, 1953, Experientia.

Expression of the mitochondria genome in HeLa cells. IV. Titration of mitochondrial genes for 16 s, 12 s and 4 s RNA.

G. Attardi, Y. Aloni, 1971, Journal of molecular biology.

Quantitative behaviour of cytoplasmic RNA in rat Purkinje cells following prolonged physiological stimulation.

G. Attardi, 1957, Experimental cell research.

The effects of sodium paraminosalicylate on the growth of pure cultures of embryo chick myoblasts

G. Attardi, B. Viterbo, D. Gandini, 1952 .

Recognition of ribosomal RNA sites in DNA. II. The HeLa cell system.

P. C. Huang, G. Attardi, S. Kabat, 1965, Proceedings of the National Academy of Sciences of the United States of America.

In vivo incorporation of different amino acids into electrophoretically characteristic polypeptides synthesized by HeLa cell mitochondria.

G. Attardi, P. Costantino, E. Ching, 1977, Biochemical and Biophysical Research Communications - BBRC.

Intercalating drugs and low temperatures inhibit synthesis and processing of ribosomal RNA in isolated human mitochondria.

G. Attardi, G. Gaines, 1984, Journal of molecular biology.

Inter-mitochondrial complementation of mtDNA mutations and nuclear context

J. Enríquez, G. Attardi, J. Cabezas-Herrera, 2002, Nature Genetics.

Mitochondrial growth and division during the cell cycle in HeLa cells

J. England, G. Attardi, J. Posakony, 1977, The Journal of cell biology.