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Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content

Nature (London), 2010-01, Vol.463 (7280), p.536-539

2010

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Extreme variability among mammalian V1R gene families

Genome research, 2010-01, Vol.20 (1), p.10

2010

Volltextzugriff (PDF)

Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication

Nature, 2005-09, Vol.437 (7055), p.94-100

2005

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Human cytogenetics: 46 chromosomes, 46 years and counting

Nature reviews. Genetics, 2002-10, Vol.3 (10), p.769-778

Trask, Barbara J

2002

Volltextzugriff (PDF)

Human subtelomeric WASH genes encode a new subclass of the WASP family

PLoS genetics, 2007-12, Vol.3 (12), p.e237-e237

2007

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Divergent V1R repertoires in five species: Amplification in rodents, decimation in primates, and a surprisingly small repertoire in dogs

Genome research, 2005-02, Vol.15 (2), p.231

2005

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Alagille syndrome is caused by mutations in human Jagged1 , which encodes a ligand for Notch1

Nature genetics, 1997-07, Vol.16 (3), p.243-251

1997

Volltextzugriff (PDF)

Elevated rates of sister chromatid exchange at chromosome ends

PLoS genetics, 2007-02, Vol.3 (2), p.e32-e32

2007

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Rigorous and thorough bioinformatic analyses of olfactory receptor promoters confirm enrichment of O/E and homeodomain binding sites but reveal no new common motifs

BMC genomics, 2011-11, Vol.12 (1), p.561-561, Article 561

2011

Volltextzugriff (PDF)

Short Inverted Repeats Initiate Gene Amplification through the Formation of a Large DNA Palindrome in Mammalian Cells

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (13), p.8772-8777

2002

Volltextzugriff (PDF)

Complex evolution of 7E olfactory receptor genes in segmental duplications

Genome research, 2003-05, Vol.13 (5), p.781

2003

Volltextzugriff (PDF)

V2R gene families degenerated in primates, dog and cow, but expanded in opossum

Trends in genetics, 2007-05, Vol.23 (5), p.212-215

2007

Volltextzugriff (PDF)

Identification of a Novel Gene on Chromosome 7q11.2 Interrupted by a Translocation Breakpoint in a Pair of Autistic Twins

Genomics (San Diego, Calif.), 2002-08, Vol.80 (2), p.129-134

2002

Volltextzugriff (PDF)

Distribution of olfactory receptor genes in the human genome

Nature genetics, 1998-03, Vol.18 (3), p.243-250

1998

Volltextzugriff (PDF)

The complex structure and dynamic evolution of human subtelomeres

Nature reviews. Genetics, 2002-02, Vol.3 (2), p.91-102

2002

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Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions

Genome research, 2002-11, Vol.12 (11), p.1663

2002

Volltextzugriff (PDF)

Tissue-specific variation in DNA methylation levels along human chromosome 1

Epigenetics & chromatin, 2009-06, Vol.2 (1), p.7-7, Article 7

2009

Volltextzugriff (PDF)

Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family

American journal of human genetics, 2008-08, Vol.83 (2), p.228-242

2008

Volltextzugriff (PDF)

Sequence Analysis of Mouse Vomeronasal Receptor Gene Clusters Reveals Common Promoter Motifs and a History of Recent Expansion

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (1), p.291-296

2002

Volltextzugriff (PDF)

Different evolutionary processes shaped the mouse and human olfactory receptor gene families

Human molecular genetics, 2002-03, Vol.11 (5), p.535-546

2002

Volltextzugriff (PDF)

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

Nature genetics, 1992-06, Vol.1 (3), p.159-165

1992

Volltextzugriff (PDF)

The sense of smell: genomics of vertebrate odorant receptors

Human molecular genetics, 2002-05, Vol.11 (10), p.1153-1160

2002

Volltextzugriff (PDF)

Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen

Molecular biology and evolution, 2005-08, Vol.22 (8), p.1712-1720

2005

Volltextzugriff (PDF)

Estimating Genomic Distance from DNA Sequence Location in Cell Nuclei by a Random Walk Model

Science (American Association for the Advancement of Science), 1992-09, Vol.257 (5075), p.1410-1412

1992

Volltextzugriff (PDF)

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

Human genetics, 1998-11, Vol.103 (5), p.590-599

1998

Volltextzugriff (PDF)

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Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content

Extreme variability among mammalian V1R gene families

Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication

Human cytogenetics: 46 chromosomes, 46 years and counting

Human subtelomeric WASH genes encode a new subclass of the WASP family

Divergent V1R repertoires in five species: Amplification in rodents, decimation in primates, and a surprisingly small repertoire in dogs

Alagille syndrome is caused by mutations in human Jagged1 , which encodes a ligand for Notch1

Elevated rates of sister chromatid exchange at chromosome ends

Rigorous and thorough bioinformatic analyses of olfactory receptor promoters confirm enrichment of O/E and homeodomain binding sites but reveal no new common motifs

Short Inverted Repeats Initiate Gene Amplification through the Formation of a Large DNA Palindrome in Mammalian Cells

Complex evolution of 7E olfactory receptor genes in segmental duplications

V2R gene families degenerated in primates, dog and cow, but expanded in opossum

Identification of a Novel Gene on Chromosome 7q11.2 Interrupted by a Translocation Breakpoint in a Pair of Autistic Twins

Distribution of olfactory receptor genes in the human genome

The complex structure and dynamic evolution of human subtelomeres

Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions

Tissue-specific variation in DNA methylation levels along human chromosome 1

Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family

Sequence Analysis of Mouse Vomeronasal Receptor Gene Clusters Reveals Common Promoter Motifs and a History of Recent Expansion

Different evolutionary processes shaped the mouse and human olfactory receptor gene families

The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

The sense of smell: genomics of vertebrate odorant receptors

Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen

Estimating Genomic Distance from DNA Sequence Location in Cell Nuclei by a Random Walk Model

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

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