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Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21

BMC genomics, 2010-03, Vol.11 (1), p.195-195, Article 195

2010

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Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Journal of molecular and cellular cardiology, 1999-05, Vol.31 (5), p.1025-1032

1999

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Recombination across the centromere of disjoined and non-disjoined chromosome 21

Human molecular genetics, 2003-09, Vol.12 (17), p.2229-2239

2003

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Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy

European journal of human genetics : EJHG, 2003-09, Vol.11 (9), p.659-664

2003

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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BAGE genes generated by juxtacentromeric reshuffling in the hominidae lineage are under selective pressure

Genomics (San Diego, Calif.), 2003-04, Vol.81 (4), p.391-399

2003

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Human centromeric alphoid domains are periodically homogenized so that they vary substantially between homologues. Mechanism and implications for centromere functioning

Nucleic acids research, 2006-01, Vol.34 (6), p.1912

Roizès, Gérard

2006

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MethDB--a public database for DNA methylation data

Nucleic acids research, 2001-01, Vol.29 (1), p.270

2001

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Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21

Human genetics, 2000-08, Vol.107 (2), p.127-131

2000

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Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences

Chromosome research, 1999-06, Vol.7 (4), p.305-317

1999

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Global analysis of DNA methylation and transcription of human repetitive sequences

Epigenetics, 2009-07, Vol.4 (5), p.339-350

2009

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MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia

Gene, 2002-02, Vol.284 (1-2), p.73-81

2002

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Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy

Journal of the American College of Cardiology, 2000-01, Vol.35 (1), p.29-35

2000

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Lack of association between polymorphisms of eight candidate genes and Idiopathic dilated cardiomyopathy : The CARDIGENE study

Journal of the American College of Cardiology, 2000, Vol.35 (1), p.29-35

2000

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DNA Methylation Database “MethDB”: a User Guide

The Journal of nutrition, 2002-08, Vol.132 (8), p.2435S-2439S

2002

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Characterization of the human tubulin tyrosine ligase-like 1 gene ( TTLL1) mapping to 22q13.1

Gene, 2000-10, Vol.257 (1), p.109-117

2000

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Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms

Gene, 2003-07, Vol.312, p.41-50

2003

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile

European journal of human genetics : EJHG, 2002-12, Vol.10 (12), p.833-840

2002

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Analysis of eucaryotic DNAs with a restriction endonuclease from H.influenzae: isolation of “hidden” satellite DNAs

Nucleic acids research, 1974-09, Vol.1 (9), p.1099-1120

Roizes, Gerard

1974

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A 37-kb Fragment Common to the Pericentromeric Region of Human Chromosomes 13 and 21 and to the Ancestral Inactive Centromere of Chromosome 2

Genomics (San Diego, Calif.), 1993-03, Vol.15 (3), p.576-581

1993

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Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen

Genomics (San Diego, Calif.), 1999-03, Vol.56 (3), p.274-287

1999

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Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments

Gene, 1999-10, Vol.239 (1), p.55-64

1999

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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Risk Scores in ST-Segment Elevation Myocardial Infarction Patients with Refractory Cardiogenic Shock and Veno-Arterial Extracorporeal Membrane Oxygenation

Journal of clinical medicine, 2021-03, Vol.10 (5), p.956

2021

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Molecular and evolutionary characteristics of the fraction of human alpha satellite DNA associated with CENP-A at the centromeres of chromosomes 1, 5, 19, and 21

Characterization of a Unique Genetic Variant in the β1-adrenoceptor Gene and Evaluation of its Role in Idiopathic Dilated Cardiomyopathy

Recombination across the centromere of disjoined and non-disjoined chromosome 21

Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

BAGE genes generated by juxtacentromeric reshuffling in the hominidae lineage are under selective pressure

Human centromeric alphoid domains are periodically homogenized so that they vary substantially between homologues. Mechanism and implications for centromere functioning

MethDB--a public database for DNA methylation data

Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21

Hypothesis: for the worst and for the best, L1Hs retrotransposons actively participate in the evolution of the human centromeric alphoid sequences

Global analysis of DNA methylation and transcription of human repetitive sequences

MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia

Lack of association between polymorphisms of eight candidate genes and idiopathic dilated cardiomyopathy

Lack of association between polymorphisms of eight candidate genes and Idiopathic dilated cardiomyopathy : The CARDIGENE study

DNA Methylation Database “MethDB”: a User Guide

Characterization of the human tubulin tyrosine ligase-like 1 gene ( TTLL1) mapping to 22q13.1

Juxtacentromeric region of human chromosome 21: a boundary between centromeric heterochromatin and euchromatic chromosome arms

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

New BAGE (B melanoma antigen) genes mapping to the juxtacentromeric regions of human chromosomes 13 and 21 have a cancer/testis expression profile

Analysis of eucaryotic DNAs with a restriction endonuclease from H.influenzae: isolation of “hidden” satellite DNAs

A 37-kb Fragment Common to the Pericentromeric Region of Human Chromosomes 13 and 21 and to the Ancestral Inactive Centromere of Chromosome 2

Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen

Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

Risk Scores in ST-Segment Elevation Myocardial Infarction Patients with Refractory Cardiogenic Shock and Veno-Arterial Extracorporeal Membrane Oxygenation

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