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The DNA sequence of human chromosome 21

Nature (London), 2000-05, Vol.405 (6784), p.311-319

2000

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Disruption of the Rev3l-encoded catalytic subunit of polymerase ζ in mice results in early embryonic lethality

Current biology, 2000-10, Vol.10 (19), p.1221-1224

2000

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Gene Defect behind APECED: A New Clue to Autoimmunity

Human molecular genetics, 1998-01, Vol.7 (10), p.1547-1553

1998

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AIRE Encodes a Nuclear Protein Co-Localizing With Cytoskeletal Filaments: Altered Sub-Cellular Distribution of Mutants Lacking the PHD Zinc Fingers

Human molecular genetics, 1999-02, Vol.8 (2), p.277-290

1999

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Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

Genome research, 2004-07, Vol.14 (7), p.1258-1267

2004

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Taking a functional genomics approach in molecular medicine

Trends in Molecular Medicine, 2001-11, Vol.7 (11), p.494-501

Yaspo, Marie-Laure

2001

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C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation

Leukemia, 2018-03, Vol.32 (3), p.828-836

2018

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Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis (Part I)

Amino acids, 2003-01, Vol.24 (1-2), p.111-117

2003

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Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries

Human molecular genetics, 1995-08, Vol.4 (8), p.1291-1304

1995

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Construction and Analysis of a Human-Chimpanzee Comparative Clone Map

Science (American Association for the Advancement of Science), 2002-01, Vol.295 (5552), p.131-134

2002

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Down Syndrome-Critical Region Contains a Gene Homologous to Drosophila sim Expressed During Rat and Human Central Nervous System Development

Proceedings of the National Academy of Sciences - PNAS, 1995-09, Vol.92 (20), p.9191-9195

1995

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S146 DECIPHERING THE ROLE OF RUNX1 ISOFORMS IN THE DEVELOPMENT OF TRANSIENT ABNORMAL MYELOPOIESIS

HemaSphere, 2019-06, Vol.3 (S1), p.25-n/a

2019

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A new member of the proprotein convertase gene family (LPC) is located at a chromosome translocation breakpoint in lymphomas

Cancer research (Chicago, Ill.), 1996-02, Vol.56 (3), p.448-451

1996

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DNA sequence and comparative analysis of chimpanzee chromosome 22

Nature, 2004-05, Vol.429 (6990), p.382-388

2004

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Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginine N-methyltransferase 1 (PRMT1) gene

Mammalian genome, 1997-07, Vol.8 (7), p.526-529

1997

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An integrated YAC-overlap and ‘cosmid-pocket’ map of the human chromosome 21

Human molecular genetics, 1994-05, Vol.3 (5), p.759-770

1994

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Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome

Genome research, 1998-04, Vol.8 (4), p.385-398

1998

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A New Inward Rectifier Potassium Channel Gene (KCNJ15) Localized on Chromosome 21 in the Down Syndrome Chromosome Region 1 (DCR1)

Genomics (San Diego, Calif.), 1997-09, Vol.44 (2), p.237-241

1997

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Cloning of a Novel Human Putative Type Ia Integral Membrane Protein Mapping to 21q22.3

Genomics (San Diego, Calif.), 1998-04, Vol.49 (1), p.133-136

1998

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Characterization of a Novel Gene, C21orf6, Mapping to a Critical Region of Chromosome 21q22.1 Involved in the Monosomy 21 Phenotype and of Its Murine Ortholog, orf5

Genomics (San Diego, Calif.), 2000-03, Vol.64 (2), p.203-210

2000

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An efficient and economic enhancer mix for PCR

Biochemical and biophysical research communications, 2006-09, Vol.347 (3), p.747-751

2006

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847P Precision oncology for resistant acral, mucosal and cutaneous melanomas: A prospective broad high throughput genomics feasibility study

Annals of oncology, 2022-09, Vol.33, p.S937

2022

Volltextzugriff (PDF)

Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

Genomics (San Diego, Calif.), 1998-02, Vol.48 (1), p.12-23

1998

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Report of the seventh international workshop on human chromosome 21 mapping 1997

Cytogenetic and genome research, 1998, Vol.82 (1-2), p.1-12

1998

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The DNA sequence of human chromosome 21

Disruption of the Rev3l-encoded catalytic subunit of polymerase ζ in mice results in early embryonic lethality

Gene Defect behind APECED: A New Clue to Autoimmunity

AIRE Encodes a Nuclear Protein Co-Localizing With Cytoskeletal Filaments: Altered Sub-Cellular Distribution of Mutants Lacking the PHD Zinc Fingers

Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome

Taking a functional genomics approach in molecular medicine

C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation

Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis (Part I)

Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries

Construction and Analysis of a Human-Chimpanzee Comparative Clone Map

Down Syndrome-Critical Region Contains a Gene Homologous to Drosophila sim Expressed During Rat and Human Central Nervous System Development

S146 DECIPHERING THE ROLE OF RUNX1 ISOFORMS IN THE DEVELOPMENT OF TRANSIENT ABNORMAL MYELOPOIESIS

A new member of the proprotein convertase gene family (LPC) is located at a chromosome translocation breakpoint in lymphomas

DNA sequence and comparative analysis of chimpanzee chromosome 22

Identification and mapping of a novel human gene, HRMT1L1, homologous to the rat protein arginine N-methyltransferase 1 (PRMT1) gene

An integrated YAC-overlap and ‘cosmid-pocket’ map of the human chromosome 21

Bacterial contig map of the 21q11 region associated with Alzheimer's disease and abnormal myelopoiesis in Down syndrome

A New Inward Rectifier Potassium Channel Gene (KCNJ15) Localized on Chromosome 21 in the Down Syndrome Chromosome Region 1 (DCR1)

Cloning of a Novel Human Putative Type Ia Integral Membrane Protein Mapping to 21q22.3

Characterization of a Novel Gene, C21orf6, Mapping to a Critical Region of Chromosome 21q22.1 Involved in the Monosomy 21 Phenotype and of Its Murine Ortholog, orf5

An efficient and economic enhancer mix for PCR

847P Precision oncology for resistant acral, mucosal and cutaneous melanomas: A prospective broad high throughput genomics feasibility study

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome

Transcriptional Map of the 2.5-Mb CBR–ERG Region of Chromosome 21 Involved in Down Syndrome

Report of the seventh international workshop on human chromosome 21 mapping 1997

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