M. Lott

发表

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

A. Torroni, D. Wallace, M. Lott, 1994, American journal of human genetics.

Mitochondrial DNA variation in human evolution and disease.

D. Wallace, M. Lott, M. Brown, 1999, Gene.

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

D. Wallace, M. Lott, T. Schurr, 1988, Science.

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

D. Wallace, M. Lott, S. Ballinger, 1990, Cell.

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

B. Crain, M. Gearing, S. Mirra, 1993, Genomics.

Analysis of mitochondrial DNA diversity in the aleuts of the commander islands and its implications for the genetic history of beringia.

R. Sukernik, D. Wallace, M. Lott, 2002, American journal of human genetics.

Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation

Larry N. Singh, Marni J. Falk, M. Attimonelli, 2020, Human mutation.

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.

N. Newman, E. Stone, D. Wallace, 1992, Journal of clinical neuro-ophthalmology.

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV

M. Lott, J. Shoffner, N. Krawiecki, 1989, Neurology.

Toward a mtDNA locus‐specific mutation database using the LOVD platform

Q. Kong, D. Wallace, A. Salas, 2012, Human mutation.

Computer prediction of peptide maps: assignment of polypeptides to human and mouse mitochondrial DNA genes by analysis of two-dimensional-proteolytic digest gels.

J. H. Yang, D. Wallace, M. Lott, 1986, American journal of human genetics.

MSeqDR mvTool: A mitochondrial DNA Web and API resource for comprehensive variant annotation, universal nomenclature collation, and reference genome conversion

Marni J. Falk, M. Attimonelli, Lishuang Shen, 2018, Human mutation.

Abstracts for the committee on the genetic constitution of chromosome 1

Brien, J. Beckmann, K. Kidd, 1991 .

MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences

Pierre Baldi, Vincent Procaccio, Eduardo Ruiz-Pesini, 2009, Human mutation.

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

N. Newman, D. Wallace, M. Lott, 1991, American journal of ophthalmology.

Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team.

N. Newman, A. Torroni, D. Wallace, 1994, American journal of ophthalmology.

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.

D. Wallace, M. Lott, G. Singh, 1989, The New England journal of medicine.

Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3)

Brien, J. Beckmann, K. Kidd, 1991 .

Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.

D. Wallace, M. Lott, J. Shoffner, 1991, JAMA.

Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP

Vincent Procaccio, Marie T. Lott, Douglas C. Wallace, 2017, PLoS Comput. Biol..

Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.

D. Wallace, M. Lott, 2017, Handbook of experimental pharmacology.

mtDNA Variation and Analysis Using Mitomap and Mitomaster

Mahdi Sarmady, Vincent Procaccio, Jeremy Leipzig, 2013, Current protocols in bioinformatics.

Variable genotype of Leber's hereditary optic neuropathy patients.

D. Wallace, M. Lott, A. Voljavec, 1990, American journal of ophthalmology.

Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.

Marcella Attimonelli, Xiaowu Gai, Lishuang Shen, 2015, Molecular genetics and metabolism.

Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups

E. Starikovskaya, R. Sukernik, A. Torroni, 2005, Annals of human genetics.

Mitochondrial Biology and Medicine

D. Wallace, M. Lott, V. Procaccio, 2019, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases

D. Wallace, M. Lott, M. Brown, 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

C. Epstein, D. Wallace, M. Lott, 1988, Cell.

TARGETED DOWN REGULATION OF CORE MITOCHONDRIAL GENES DURING SARS-COV-2 INFECTION

Larry N. Singh, Amanda M. Saravia-Butler, Yared H. Kidane, 2022, bioRxiv.

Mitochondrial DNA variation and cancer

Larry N. Singh, D. Wallace, M. Lott, 2021, Nature Reviews Cancer.

An enhanced MITOMAP with a global mtDNA mutational phylogeny

Pierre Baldi, Vincent Procaccio, Marie T. Lott, 2006, Nucleic Acids Res..

MITOMAP: a human mitochondrial genome database—2004 update

Shamkant B. Navathe, Pierre Baldi, Marie T. Lott, 2004, Nucleic Acids Res..

Title An enhanced MITOMAP with a global mtDNA mutational phylogeny Permalink

Marty C. Brandon, P. Baldi, D. Wallace, 2006 .

MITOMAP: a human mitochondrial genome database--1998 update

Shamkant B. Navathe, Michael D. Brown, Andreas M. Kogelnik, 1998, Nucleic Acids Res..

Mitochondria1 encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene

D. Wallace, M. Lott, J. Shoffner, 1995, Neurology.

Mitochondrial DNA Mutations and the Eye

D. Wallace, M. Lott, Michael D. Brown, 1994 .

The Mitochondrial Genome and Human Mitochondrial Diseases

E. Starikovskaya, R. Sukernik, D. Wallace, 2002, Russian Journal of Genetics.

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

D. Wallace, M. Lott, J. Shoffner, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.

D. Wallace, M. Lott, J. Shoffner, 1992, Mutation research.

mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.

A. Torroni, D. Wallace, O. Semino, 1994, American journal of human genetics.

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.

M. Beal, D. Wallace, A. McKee, 1994, Genomics.

Novel mtDNA Imparts the Connective Tissue Disorder of a Tourette Pedigree

D. Wallace, M. Lott, Kierstin N Keller, 2022, bioRxiv.

Mitochondrial DNA Complex I and I11 Mutations Associated With Leber’s Hereditary Optic Neuropathy

A. Torroni, D. Wallace, M. Lott, 2002 .

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

M. Beal, D. Wallace, M. Lott, 1992, Nature Genetics.

Mitochondrial Medicine: The Mitochondrial Biology and Genetics of Metabolic and Degenerative Diseases, Cancer, and Aging

D. Wallace, M. Lott, P. Vincent, 2014 .

MERRF: a model disease for understanding the principles of mitochondrial genetics.

D. Wallace, M. Lott, J. Shoffner, 1991, Revue neurologique.

Atypical Leber's hereditary optic neuropathy with molecular confirmation.

N. Newman, D. Wallace, M. Lott, 1993, Archives of neurology.

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

A. Torroni, D. Wallace, M. Lott, 1992, American journal of human genetics.

Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy.

N. Newman, S. Manoukian, D. Wallace, 1992, American journal of ophthalmology.

Mitochondrial biology, degenerative diseases and aging

S. Melov, D. Wallace, M. Lott, 1998, BioFactors.

Diseases resulting from mitochondrial DNA point mutations

D. Wallace, M. Lott, M. Brown, 1992, Journal of Inherited Metabolic Disease.

Combination of common mtDNA variants results in mitochondrial dysfunction and a connective tissue dysregulation

D. Murdock, D. Wallace, M. Lott, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction

D. Wallace, M. Lott, J. Shoffner, 1990, Pediatric Research.

Cuban optic neuropathy

N. Newman, A. Torroni, D. Wallace, 1995, Neurology.

Mitochondrial DNA Mutations in Epilepsy and Neurological Disease

D. Wallace, M. Lott, S. Ballinger, 1994, Epilepsia.

African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba

N. Newman, A. Torroni, D. Wallace, 1995, Human mutation.

MITOMAP: a human mitochondrial genome database--1998 update

Shamkant B. Navathe, Michael D. Brown, Andreas M. Kogelnik, 1998, Nucleic Acids Res..

MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease

Marcella Attimonelli, Lishuang Shen, Jeremy Leipzig, 2016, Human mutation.

Subacute necrotizing encephalopathy

D. A. Koontz, P. Fernhoff, N. Newman, 1992, Neurology.

Bioinformatics resources, databases, and tools for human mtDNA

Marcella Attimonelli, Vincent Procaccio, Marie T. Lott, 2020 .

Diseases esulting fro Point Mutations

D. Wallace, M. Lott, J. Shoffner, 1992 .

Epidemic Neuropathy in Cuba Not Associated with Mitochondria1 DNA Mutations Found in Leber??s Hereditary Optic Neuropathy Patient

N. Newman, A. Torroni, M. Lott, 1995 .

Mitochondrial DNA mutations in human degenerative diseases and aging.

D. Wallace, M. Lott, S. Ballinger, 1995, Biochimica et biophysica acta.

MITOMAP: an update on the status of the human mitochondrial genome database

Shamkant B. Navathe, Michael D. Brown, Andreas M. Kogelnik, 1997, Nucleic Acids Res..

APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants

Salvatore Daniele Bianco, T. Mazza, A. Vescovi, 2023, bioRxiv.

Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.

A. Torroni, D. Wallace, M. Lott, 1994, American journal of human genetics.

Abstracts for the committee on the genetic constitution of chromosome 6

Brien, J. Beckmann, K. Kidd, 1991 .

Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts

Larry N. Singh, Amanda M. Saravia-Butler, Yared H. Kidane, 2023, Science Translational Medicine.

Abstracts for the committee on comparative gene mapping

Brien, J. Beckmann, K. Kidd, 1991 .

Phy-Mer: a novel alignment-free and reference-independent mitochondrial haplogroup classifier

Janey L. Wiggs, Lishuang Shen, Marie T. Lott, 2015, Bioinform..

Abstracts for the committee on the genetic constitution of chromosome 15

Brien, J. Beckmann, K. Kidd, 1991 .

a human mitochondrial

Marty C. Brandon, S. Navathe, M. Lott, 2004 .

MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease

Marni J. Falk, M. Attimonelli, Lishuang Shen, 2016, Human mutation.