S. Ottolenghi

发表

A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level γ-Globin Inducing Compounds

F. Gasparri, P. Cappella, Mario Mauri, 2015, PloS one.

Sox2 deficiency causes neurodegeneration and impaired neurogenesis in the adult mouse brain

Pier Paolo Pandolfi, Annalisa Canta, Annamaria Vezzani, 2004, Development.

Bone marrow-derived cells can acquire cardiac stem cells properties in damaged heart

E. Kizana, E. Messina, S. Ottolenghi, 2009, Journal of cellular and molecular medicine.

Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele

M. Pontoglio, R. Taramelli, C. Vergani, 1990, Human Genetics.

The gene encoding DRAP (BACE2), a glycosylated transmembrane protein of the aspartic protease family, maps to the Down critical region

F. Acquati, R. Taramelli, L. Jovine, 2000, FEBS letters.

Deletion of a Negatively Acting Sequence in a Chimeric GATA-1 Enhancer-Long Terminal Repeat Greatly Increases Retrovirally Mediated Erythroid Expression*

G. Ferrari, F. Lotti, S. Ottolenghi, 2004, Journal of Biological Chemistry.

An erythroid specific enhancer upstream to the gene encoding the cell-type specific transcription factor GATA-1.

S. Nicolis, L. Lanfranco, S. Ottolenghi, 1991, Nucleic acids research.

An erythroid specific nuclear factor binding to the proximal CACCC box of the beta-globin gene promoter.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1988, Nucleic acids research.

SOHLH1 and SOHLH2 control Kit expression during postnatal male germ cell development

M. Gori, P. Rossi, E. Jannini, 2012, Journal of Cell Science.

Dependence for the proliferative response to erythropoietin on an established erythroid differentiation program in a human hematopoietic cell line, UT-7.

J. Adamson, M. Baiocchi, A. Migliaccio, 1993, Experimental hematology.

Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

δβ-Thalassemia is due to a gene deletion

J. Clegg, D. Weatherall, W. Lanyon, 1976, Cell.

Transcriptional and Post‐transcriptional Defects in β0‐Thalassaemia

R. Williamson, G. Masera, S. Ottolenghi, 1977 .

Delta thalassemia: a non-deletion defect.

R. Taramelli, S. Ottolenghi, B. Giglioni, 2005, European journal of biochemistry.

Alternatively spliced mRNAs encoding soluble isoforms of the erythropoietin receptor in murine cell lines and bone marrow.

J. Adamson, Y. Jiang, A. Migliaccio, 1994, Gene.

Sox2‐dependent maintenance of mouse oligodendroglioma involves the Sox2‐mediated downregulation of Cdkn2b, Ebf1, Zfp423, and Hey2

L. Ricci-Vitiani, R. Pallini, R. Favaro, 2020, Glia.

Sox2 transgene expression in neural stem cells

R. Lovell-Badge, R. Galli, A. Vescovi, 2000 .

The "bystander effect": association of U-87 cell death with ganciclovir-mediated apoptosis of nearby cells and lack of effect in athymic mice.

G. Finocchiaro, B. Pollo, S. Benedetti, 1995, Human gene therapy.

The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

Delta-beta-thalassemia is due to a gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

Globin -chain synthesis directed by "supernatant" 10S RNA from rabbit reticulocytes.

G. Guidotti, S. Ottolenghi, B. Giglioni, 1972, Nature: New biology.

To respond or not to respond to hydroxyurea in thalassemia: a matter of stress adaptation?

S. Ottolenghi, A. Ronchi, 2013, Haematologica.

Sox6 enhances erythroid differentiation in human erythroid progenitors.

S. Piconese, G. Ferrari, C. Fugazza, 2011, Blood.

Direct demonstration of β-globin mRNA in homozygous Ferrara β0-thalassaemia patients

R. Williamson, S. Ottolenghi, B. Giglioni, 1977, Nature.

Presence of gene for β globin in homozygous β0 thalassaemia

R. Williamson, J. Clegg, D. Weatherall, 1976, Nature.

A gene controlling fetal hemoglobin expression in adults is not linked to the non‐alpha globin cluster.

R. Taramelli, M. Cappellini, S. Ottolenghi, 1983, The EMBO journal.

Functional Interaction of CP2 with GATA-1 in the Regulation of Erythroid Promoters

S. Jane, J. Cunningham, C. Fugazza, 2006, Molecular and Cellular Biology.

Molecular heterogeneity of regulatory elements of the mouse GATA-1 gene.

P. Ricciardi-Castagnoli, J. Ghysdael, S. Ottolenghi, 1997, Genes and function.

Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease

G. Masera, S. Ottolenghi, B. Giglioni, 1979, Nature.

β-Thalassemic Syndromes As a Model for the Study of the Molecular Basis of Human Inherited Disease

R. Mantovani, G. Saglio, S. Nicolis, 1987 .

Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

R. Taramelli, M. Baiget, G. Saglio, 1982, Proceedings of the National Academy of Sciences of the United States of America.

A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta‐thalassemia.

R. Mantovani, G. Saglio, S. Ottolenghi, 1984, The EMBO journal.

Acetylation and MAPK phosphorylation cooperate to regulate the degradation of active GATA‐1

H. Beug, S. Ottolenghi, M. Ciró, 2006 .

Activation of Erythroid-Specif ic Promoters During Anthracycline-Induced Differentiation of K 562 Cells

A. Doubeikovski, S. Ottolenghi, P. Jeannesson, 2002 .

Expression of GATA-1 mRNA in human myeloid leukemic cells.

F. Lo Coco, G. Saglio, S. Nicolis, 1994, Leukemia.

A Novel Type of c‐myc Translocation in a T Lymphoma Cell Line a

M. Rocchi, G. Saglio, S. Ottolenghi, 1987, Annals of the New York Academy of Sciences.

Molecular characterisation of the human apo(a)-plasminogen gene family clustered on the telomeric region of chromosome 6 (6q26-27).

F. Acquati, R. Taramelli, E. Citterio, 1994, Human molecular genetics.

Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.

R. Williamson, J. Clegg, D. Weatherall, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Cellular Biology Cardiomyogenesis in the Developing Heart Is Regulated by C-Kit–Positive Cardiac Stem Cells

A. Matsuda, João Ferreira-Martins, Fumihiro Sanada, 2012 .

Regulation of γ‐Globin Expression in Hereditary Persistence of Fetal Hemoglobin

S. Nicolis, S. Ottolenghi, A. Ronchi, 1990 .

Sox2-dependent maintenance of mouse oligodendroglioma involves the Sox2-mediated downregulation of Cdkn2b, Ebf1, Zfp423 and Hey2

L. Ricci-Vitiani, R. Pallini, R. Favaro, 2020, bioRxiv.

Erythroid-specific activation of the distal (testis) promoter of GATA1 during differentiation of purified normal murine hematopoietic stem cells.

A. Migliaccio, G. Migliaccio, S. Ottolenghi, 1996, Acta haematologica.

Cellular Differentiation in the Hematopoietic System: an Introduction

S. Ottolenghi, M. Introna, J. Golay, 1992 .

A 3' truncation of MYC caused by chromosomal translocation in a human T-cell leukemia increases mRNA stability.

J. Bishop, G. Saglio, S. Ottolenghi, 1990, Oncogene.

substitution at position -196 of the A gamma globin gene promoter Sardinian delta beta zero-thalassemia: a further example of a C to T

G. Saglio, S. Ottolenghi, C. Camaschella, 2011 .

A frequent Aγ-persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with β-thalassemia

G. Saglio, M. Pirastu, S. Ottolenghi, 1988, Human Genetics.

Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoter.

G. Saglio, S. Ottolenghi, C. Camaschella, 1987, Blood.

Biosynthesis of globin chains in fetal liver and adult marrow cultures.

C. Peschle, A. Migliaccio, G. Migliaccio, 1981, Experimental cell research.

Hemoglobin synthesis in individual bursts from normal adult blood: all bursts and subcolonies synthesize G gamma-and A gamma-globin chains

Cappellini, C. Peschle, M. Condorelli, 1980 .

Hemoglobin synthesis in individual bursts from normal adult blood: all bursts and subcolonies synthesize G gamma-and A gamma-globin chains.

C. Peschle, M. Condorelli, A. Migliaccio, 1980, Blood.

The deletion in a type of delta 0-beta 0-thalassaemia begins in an inverted AluI repeat.

S. Ottolenghi, B. Giglioni, 1982, Nature.

Defective erythroid maturation in gelsolin mutant mice

W. Witke, G. Barbarani, S. Ottolenghi, 2012, Haematologica.

Response to erythropoietin in erythroid subclones of the factor-dependent cell line 32D is determined by translocation of the erythropoietin receptor to the cell surface.

J. Adamson, A. D’Andrea, M. Baiocchi, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Globin RNA sequences in human leukaemic peripheral blood

S. Ottolenghi, B. Giglioni, A. Gianni, 1978, Nature.

Heterogeneity of δ, β‐Thalassemia and Hereditary Persistence of Hb F in the Mediterranean Area a

R. Mantovani, G. Saglio, S. Ottolenghi, 1985 .

A cis-acting DNA signal for encapsidation of simian virus 40

S. Nicolis, S. Ottolenghi, A. Oppenheim, 1992, Journal of virology.

Adult c-kitpos Cardiac Stem Cells Are Necessary and Sufficient for Functional Cardiac Regeneration and Repair

Ciro Indolfi, Angelo Leone, Giuseppe Viglietto, 2013, Cell.

Dissociation of single ribosomes as a preliminary step for their participation in protein synthesis.

G. Guidotti, S. Ottolenghi, B. Giglioni, 1973, European journal of biochemistry.

vitro model for reactivation of human fetal globin genes Bromodeoxyuridine treatment of normal adult erythroid colonies: an in

C. Peschle, G. Migliaccio, S. Ottolenghi, 2011 .

Bromodeoxyuridine treatment of normal adult erythroid colonies: an in vitro model for reactivation of human fetal globin genes.

C. Peschle, A. Migliaccio, G. Migliaccio, 1986, Blood.

A Model for Hemoglobin F Synthesis in Adult Life: Evidence for Regulation at the Level of Erythroblasts a

C. Peschle, A. Migliaccio, G. Migliaccio, 1985, Annals of the New York Academy of Sciences.

Human globin chain separation by isoelectric focusing.

L. Rossi-Bernardi, P. Righetti, S. Ottolenghi, 1979, Journal of Biochemical and Biophysical Methods.

Human T gamma globin chain is a variant of A gamma chain (A gamma Sardinia).

G. Saglio, P. Righetti, S. Ottolenghi, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Gγ and Aγ globin chains separation and quantitation by isoelectric focusing

G. Saglio, P. Righetti, S. Ottolenghi, 1979 .

bursts and subcolonies synthesize G gamma-and A gamma-globin chains Hemoglobin synthesis in individual bursts from normal adult blood: all

M. Condorelli, G. Migliaccio, S. Ottolenghi, 2011 .

DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobin.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1989, Hemoglobin.

Sardinian G gamma-HPFH: a T----C substitution in a conserved "octamer" sequence in the G gamma-globin promoter.

R. Mantovani, R. Taramelli, S. Nicolis, 1988, Blood.

Biosynthesis of Hb in individual fetal liver bursts. gamma-Chain production peaks earlier than beta-chain in the erythropoietic pathway.

C. Peschle, A. Migliaccio, G. Migliaccio, 1980, Experimental cell research.

Globin chain synthesis in single erythroid bursts from cord blood: studies on gamma leads to beta and G gamma leads to A gamma switches.

C. Peschle, M. Condorelli, G. Migliaccio, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Preferential induction of fetal versus embryonic globin chains in human leukemic cell lines.

C. Peschle, G. Saglio, S. Ottolenghi, 1982, Leukemia research.

Isoelectric Focusing of Globin Chains for Antenatal Diagnosis of β°-Thalassemia

A. Cao, S. Ottolenghi, B. Giglioni, 1981 .

Sox2 regulatory sequences direct expression of a (beta)-geo transgene to telencephalic neural stem cells and precursors of the mouse embryo, revealing regionalization of gene expression in CNS stem cells.

R. Lovell-Badge, R. Galli, A. Vescovi, 2000, Development.

Polymorphisms of human γ-globin genes in Mediterranean populations

P. Little, R. Williamson, R. Flavell, 1979, Nature.

A direct estimate of the number of human γ-globin genes

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

Antenatal diagnosis of haemoglobinopathies by improved method of isoelectric focusing of haemoglobins

B. Brambati, S. Ottolenghi, A. Crema, 1984, British journal of haematology.

High Hb F levels in a Sardinian family: a genetic defect intermediate between HPFH Greek type and delta beta-thalassemia?

M. Cappellini, G. Saglio, S. Ottolenghi, 1982, Haematologica.

Human globin gene expression and linkage in bone marrow and fetal liver.

R. Williamson, W. Lanyon, S. Ottolenghi, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Constitutive expression of GATA-1, EPOR, alpha-globin, and gamma-globin genes in myeloid clonogenic cells from juvenile chronic myelocytic leukemia.

S. Bernasconi, G. Masera, S. Ottolenghi, 1995, Blood.

Progressive inactivation of the expression of an erythroid transcriptional factor in GM- and G-CSF-dependent myeloid cell lines.

A. Migliaccio, S. Nicolis, G. Migliaccio, 1990, Nucleic acids research.

A protein factor binding to an octamer motif in the gamma-globin promoter disappears upon induction of differentiation and hemoglobin synthesis in K562 cells.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1987, Nucleic acids research.

Developmental Regulation of Human Globin Genes: a Model for Cell Differentiation in the Hematopoietic System

S. Ottolenghi, 1992 .

Erythropoietin triggers a burst of GATA-1 in normal human erythroid cells differentiating in tissue culture.

A. Oppenheim, S. Ottolenghi, A. Ronchi, 1993, Nucleic acids research.

Increased erythrold-specific expression of a mutated HPFH γ-globin promoter requires the erythroid factor NFE-1

R. Mantovani, S. Nicolis, S. Ottolenghi, 1989 .

Altered binding to the gamma-globin promoter of two erythroid specific nuclear proteins in different HPFH syndromes.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1989, Progress in clinical and biological research.

The effects of HPFH mutations in the human gamma-globin promoter on binding of ubiquitous and erythroid specific nuclear factors.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1988, Nucleic acids research.

The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein.

G. Superti-Furga, R. Mantovani, S. Ottolenghi, 1989, Nucleic acids research.

The homozygous state of G to A--117A gamma hereditary persistence of fetal hemoglobin.

R. Taramelli, S. Ottolenghi, C. Camaschella, 1989, Blood.

Role of the duplicated CCAAT box region in gamma‐globin gene regulation and hereditary persistence of fetal haemoglobin.

S. Raguz, F. Grosveld, N. Dillon, 1996, The EMBO journal.

Differential Binding of the NFE3 and CP1/NFY Transcription Factors to the Human γ- and ε-Globin CCAAT Boxes (*)

C. Mazzucchelli, S. Ottolenghi, A. Ronchi, 1995, The Journal of Biological Chemistry.

Sox2 is required to maintain cancer stem cells in a mouse model of high-grade oligodendroglioma.

M. Foti, G. Finocchiaro, R. Favaro, 2014, Cancer research.

Hippocampal development and neural stem cell maintenance require Sox2-dependent regulation of Shh

Jessica Mariani, Verdon Taylor, V. Taylor, 2009, Nature Neuroscience.

Impaired generation of mature neurons by neural stem cells from hypomorphic Sox2 mutants

Jessica Mariani, Enzo Wanke, Francesca Gullo, 2008, Development.

of Fetal Hemoglobin

R. Taramelli, S. Ottolenghi, C. Camaschella, 2017 .

Isolation and characterization of a family of sequences dispersed on the human X chromosome.

R. Heilig, G. Camerino, J. Mandel, 1988, Genomics.

FOS Rescues Neuronal Differentiation of Sox2-Deleted Neural Stem Cells by Genome-Wide Regulation of Common SOX2 and AP1(FOS-JUN) Target Genes

G. Pavesi, C. Ngan, S. Nicolis, 2021, Cells.

Sox2-Dependent Regulation of Neural Stem Cells and CNS Development

R. Favaro, S. Nicolis, J. Mariani, 2016 .

Summary Sox 2 deficiency causes neurodegeneration and impaired neurogenesis in the adult mouse brain

P. Pandolfi, A. Vezzani, S. Nicolis, 2004 .

Conserved POU Binding DNA Sites in the Sox2 Upstream Enhancer Regulate Gene Expression in Embryonic and Neural Stem Cells*

H. Schöler, R. Favaro, S. Nicolis, 2004, Journal of Biological Chemistry.

Computer sequence analysis of human highly conserved zinc finger modules.

S. Ottolenghi, R. Chiaramonte, E. Bartolini, 1998, DNA sequence : the journal of DNA sequencing and mapping.

Transcriptional targeting of retroviral vectors to the erythroblastic progeny of transduced hematopoietic stem cells.

F. Mavilio, G. Ferrari, A. Aiuti, 1999, Blood.

Sox2 controls neural stem cell self‐renewal through a Fos‐centered gene regulatory network

G. Pavesi, Chia-Lin Wei, M. Chiara, 2021, Stem cells.

Sox2 controls neural stem cell self-renewal through a Fos-centered gene regulatory network

G. Pavesi, Chia-Lin Wei, M. Chiara, 2020, bioRxiv.

β-Globin mRNA in Ferrara β0-thalassaemia (reply)

R. Williamson, S. Ottolenghi, B. Giglioni, 1977, Nature.

Functional analysis of the human lecithin cholesterol acyl transferase gene promoter.

M. Pontoglio, R. Taramelli, S. Ottolenghi, 1991, Biochemical and biophysical research communications.

An erythroid and megakaryocytic common precursor cell line (B1647) expressing both c‐mpl and erythropoietin receptor (Epo‐R) proliferates and modifies globin chain synthesis in response to megakaryocyte growth and development factor (MGDF) but not to erythropoietin (Epo)

P. Strippoli, A. Vannucchi, L. Bonsi, 1997, British journal of haematology.

NF-Y binding to twin CCAAT boxes: role of Q-rich domains and histone fold helices.

R. Mantovani, S. Ottolenghi, A. di Silvio, 1999, Journal of molecular biology.

Sox2 is required for embryonic development of the ventral telencephalon through the activation of the ventral determinants Nkx2.1 and Shh

Leonardo Beccari, P. Bovolenta, R. Favaro, 2013, Development.

Translational control of globin synthesis by haemin in Xenopus oocytes.

S. Ottolenghi, B. Giglioni, A. Gianni, 1973, Nature: New biology.

Immortalization of neuro-endocrine cells from adrenal tumors arising in SV40 T-transgenic mice

P. Ricciardi-Castagnoli, S. Ottolenghi, M. Minuzzo, 1997, Oncogene.

Mapping the Global Chromatin Connectivity Network for Sox2 Function in Neural Stem Cell Maintenance

P. Bovolenta, G. Pavesi, P. Robson, 2019, Cell stem cell.

A human leukemic T-cell line bears an abnormal and overexpressed c-myc gene: molecular and functional characterization of the rearrangement.

M. Rocchi, G. Saglio, S. Ottolenghi, 1987, Haematology and blood transfusion.

Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced by his) carriers.

R. Taramelli, M. Cappellini, S. Ottolenghi, 1980, Blood.

Stem cell-mediated muscle regeneration is enhanced by local isoform of insulin-like growth factor 1.

G. Bernardi, A. Musarò, N. Rosenthal, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Repression of kit Expression by Plzf in Germ Cells

P. Pandolfi, R. Hobbs, P. Rossi, 2007, Molecular and Cellular Biology.

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.

B. Dallapiccola, A. Pizzuti, G. Novelli, 1997, Human molecular genetics.

A highly conserved SOX6 double binding site mediates SOX6 gene downregulation in erythroid cells

Claudio Cantú, Vito Grande, Ilaria Alborelli, 2010, Nucleic Acids Res..

Acetylation and MAPK phosphorylation cooperate to regulate the degradation of active GATA-1.

H. Beug, S. Ottolenghi, M. Ciró, 2007, The EMBO journal.

Sox2 Acts in Thalamic Neurons to Control the Development of Retina-Thalamus-Cortex Connectivity

P. Bovolenta, C. Frassoni, F. Guillemot, 2019, iScience.

Induction of globin mRNA expression by interleukin‐3 in a stem cell factor‐dependent SV‐40 T‐antigen‐immortalized multipotent hematopoietic cell line

F. Morlé, J. Starck, S. Ottolenghi, 2003, Journal of cellular physiology.

Spontaneous Calcium Oscillations Regulate Human Cardiac Progenitor Cell Growth

R. Rizzi, João Ferreira-Martins, M. Rota, 2009, Circulation research.

Involvement of mitogen-activated protein kinase in the cytokine-regulated phosphorylation of transcription factor GATA-1.

Tariq Enver, S. Tsuzuki, T. Enver, 2004, The Hematology Journal.

Inhibition of protein synthesis by aliphatic aldehydes. Failure of 2,3-dihydroxybutyraldehyde to inhibit chain initiation in reticulocyte lysates.

G. Guidotti, S. Ottolenghi, B. Giglioni, 1973, Biochimie.

The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene

J. Strouboulis, Yukio Nakamura, F. Gasparri, 2020, Haematologica.

beta-Like globin RNA sequences in hemoglobin Lepore disease.

R. Taramelli, S. Ottolenghi, B. Giglioni, 1979, European journal of biochemistry.

Cooperation and Competition between the Binding of COUP-TFII and NF-Y on Human ε- and γ-Globin Gene Promoters*

R. Mantovani, S. Ottolenghi, A. Ronchi, 2001, The Journal of Biological Chemistry.

black HPFH 1 and 2 lie within 17 kilobases The 3' ends of the deletions of Spanish delta beta zero-thalassemia and

R. Mantovani, M. Baiget, G. Saglio, 2013 .

The 3’ Ends ofthe Deletions ofSpanish /9#{176}-Thalassemia and Black HPFH

R. Mantovani, M. Baiget, G. Saglio, 2005 .

The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases

R. Mantovani, M. Baiget, G. Saglio, 1987 .

The deletion in a type of δ0-β0-thalassaemia begins in an inverted AluI repeat

S. Ottolenghi, B. Giglioni, 1982, Nature.

by his) carriers Organization of alpha-globin genes in Hb Hasharon (alpha 47 asp replaced

R. Taramelli, S. Ottolenghi, B. Giglioni, 2011 .

Pleiotropic, extragenic suppression of dna mutants in Bacillus subtilis

A. Siccardi, S. Ottolenghi, G. Mazza, 1976, Journal of bacteriology.

Verification of the in vivo activity of three distinct cis‐acting elements within the Gata1 gene promoter‐proximal enhancer in mice

Masayuki Yamamoto, Atsushi Hasegawa, R. Shimizu, 2013, Genes to cells : devoted to molecular & cellular mechanisms.

Regulation of Mouse p45 NF-E2 Transcription by an Erythroid-specific GATA-dependent Intronic Alternative Promoter*

P. Moi, S. Ottolenghi, E. Moroni, 2000, The Journal of Biological Chemistry.

hematopoietic and germ cell lineages Kit regulatory elements required for expression in developing

A. Giorgetti, S. Ottolenghi, E. Moroni, 2013 .

Green fluorescent protein transgene driven by Kit regulatory sequences is expressed in hematopoietic stem cells

S. Citterio, S. Ottolenghi, M. Magli, 2009, Haematologica.

Kit regulatory elements required for expression in developing hematopoietic and germ cell lineages.

A. Giorgetti, M. De Felici, S. Ottolenghi, 2003, Blood.

Cardiomyogenesis in the Developing Heart Is Regulated by C-Kit–Positive Cardiac Stem Cells

A. Matsuda, João Ferreira-Martins, Fumihiro Sanada, 2012, Circulation research.

NF-Y Organizes the γ-Globin CCAAT Boxes Region*

R. Mantovani, S. Ottolenghi, A. Ronchi, 1998, The Journal of Biological Chemistry.

Transcriptional and posttranscriptional regulation of the expression of the erythropoietin receptor gene in human erythropoietin-responsive cell lines.

J. Adamson, Y. Jiang, A. Migliaccio, 1993, Blood.

Definition of the transcription initiation site of human plasminogen gene in liver and non hepatic cell lines.

M. Pontoglio, R. Taramelli, S. Ottolenghi, 1990, Biochemical and biophysical research communications.

The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases.

R. Mantovani, M. Baiget, G. Saglio, 1987, Blood.

Increased expression of GATA-1 and NFE-2 erythroid-specific transcription factors during aclacinomycin-mediated differentiation of human erythroleukemic cells.

S. Ottolenghi, A. Ronchi, P. Jeannesson, 1993, Leukemia.

Evolution of the c‐kit‐Positive Cell Response to Pathological Challenge in the Myocardium

Mark A Sussman, N. Gude, E. Schaefer, 2008, Stem cells.

Increased Sp1 binding mediates erythroid-specific overexpression of a mutated (HPFH) gamma-globulin promoter.

S. Nicolis, S. Ottolenghi, A. Ronchi, 1989, Nucleic acids research.

Distamycins inhibit the binding of OTF-1 and NFE-1 transfactors to their conserved DNA elements.

R. Mantovani, M. Broggini, M. D’Incalci, 1989, Nucleic acids research.

Expression in hematopoietic cells of GATA-1 transcripts from the alternative "testis" promoter during development and cell differentiation.

A. Migliaccio, G. Migliaccio, S. Ottolenghi, 1997, Biochemical and biophysical research communications.

Sox2 conditional mutation in mouse causes ataxic symptoms, cerebellar vermis hypoplasia, and postnatal defects of Bergmann glia

G. Pavesi, F. Tempia, Chia-Lin Wei, 2018, Glia.

The Ephrin A1–EphA2 System Promotes Cardiac Stem Cell Migration After Infarction

R. Michler, P. Goichberg, João Ferreira-Martins, 2011, Circulation research.

Polyribosomal changes during inhibition of protein synthesis.

G. Guidotti, S. Ottolenghi, B. Giglioni, 1971, Biochimie.

Effects of aliphatic aldehydes on protein synthesis in cell-free systems.

G. Guidotti, S. Ottolenghi, B. Giglioni, 1970, Biochemical Journal.

GATA‐1‐independent Regulation of the Expression of the Erythropoietin Receptor (EPO‐R) Gene in a Human EPO‐dependent Cell Line, UT‐7 EPO a

J. Adamson, S. Nicolis, A. Migliaccio, 1994, Annals of the New York Academy of Sciences.

Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers

R. Favaro, S. Nicolis, J. Mariani, 2012, Nucleic acids research.

Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissues.

A. Simeone, A. Pizzuti, R. Taramelli, 1998, Genomics.

Abstract 911: Kit-Positive Cardiac Stem Cells (CSCs) Can Be Generated in Damaged Heart from Bone Marrow-Derived Cells

E. Messina, S. Ottolenghi, R. Gaetani, 2006 .

A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia.

G. Saglio, S. Ottolenghi, C. Camaschella, 1988, Human Genetics.

Mapping the gene encoding the human erythroid transcriptional factor NFE1-GF1 to Xp11.23

G. Camerino, B. Bardoni, S. Nicolis, 1991, Human Genetics.

Molecular comparison of 86f-thalas persistence of fetal hemoglobin DN regulatory area? (deletion/repetitive sequences/y-globin genes/polymorphism)

R. Taramelli, A. Cao, R. Galanello, 2016 .

Increased Spl binding mediates erythroid-specific overexpression of a mutated (HPFH) -y-globulin promoter

S. Nicolis, S. Ottolenghi, A. Ronchi, 2003 .

Increased erythroid-specific expression of a mutated HPFH gamma-globin promoter requires the erythroid factor NFE-1.

R. Mantovani, S. Nicolis, S. Ottolenghi, 1989, Nucleic acids research.