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Genome-wide mutation avalanches induced in diploid yeast cells by a base analog or an APOBEC deaminase

PLoS genetics, 2013-09, Vol.9 (9), p.e1003736

2013

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Targeted myocardial gene expression in failing hearts by RNA sequencing

Journal of translational medicine, 2016-11, Vol.14 (1), p.327-327, Article 327

2016

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Telomerase-immortalized human mammary stem/progenitor cells with ability to self-renew and differentiate

Proceedings of the National Academy of Sciences - PNAS, 2010-08, Vol.107 (32), p.14146-14151

2010

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Genome-wide expression profiling reveals transcriptomic variation and perturbed gene networks in androgen-dependent and androgen-independent prostate cancer cells

Cancer letters, 2008-01, Vol.259 (1), p.28-38

2008

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ATM, CTLA4, MNDA, and HEM1 in High versus Low CD38–Expressing B-Cell Chronic Lymphocytic Leukemia

Clinical cancer research, 2007-09, Vol.13 (18), p.5295-5304

2007

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Attachment-regulated signaling networks in the fibroblast-populated 3D collagen matrix

Scientific reports, 2013-05, Vol.3 (1), p.1880-1880, Article 1880

2013

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Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations

Genetics in medicine, 2008-04, Vol.10 (4), p.262-266

2008

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Molecular basis of environmentally induced birth defects

Annual review of pharmacology and toxicology, 2002-01, Vol.42 (1), p.181-208

2002

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Identification of two putative novel folate receptor genes in humans and mouse

Gene, 2000-11, Vol.258 (1), p.117-125

2000

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Distinct gene expression profiles in different B-cell compartments in human peripheral lymphoid organs

BMC immunology, 2004-09, Vol.5 (1), p.20-20, Article 20

2004

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Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa

Science (American Association for the Advancement of Science), 1998-06, Vol.280 (5370), p.1753-1757

1998

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Casodex treatment induces hypoxia-related gene expression in the LNCaP prostate cancer progression model

BMC urology, 2005-03, Vol.5 (1), p.5-5, Article 5

2005

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Biotin Supplementation Increases Expression of Genes Encoding Interferon-γ, Interleukin-1β, and 3-Methylcrotonyl-CoA Carboxylase, and Decreases Expression of the Gene Encoding Interleukin-4 in Human Peripheral Blood Mononuclear Cells

The Journal of nutrition, 2003-03, Vol.133 (3), p.716-719

2003

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Identification and Characterization of the Human and Mouse SLC19A3 Gene: A Novel Member of the Reduced Folate Family of Micronutrient Transporter Genes

Molecular genetics and metabolism, 2000-12, Vol.71 (4), p.581-590

2000

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18q22.3 → 18q23 deletion syndrome and cleft palate

American journal of medical genetics. Part A, 2010-04, Vol.152A (4), p.1046-1048

2010

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Isolation of a Gene Encoding a Novel Member of the Nuclear Receptor Superfamily from the Critical Region of Usher Syndrome Type IIa at 1q41

Genomics (San Diego, Calif.), 1998-06, Vol.50 (3), p.382-384

1998

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Identification of the Mouse and Rat Orthologs of the Gene Mutated in Usher Syndrome Type IIA and the Cellular Source of USH2A mRNA in Retina, a Target Tissue of the Disease

Genomics (San Diego, Calif.), 2002-08, Vol.80 (2), p.195-203

2002

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Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32

Genomics (San Diego, Calif.), 1997-07, Vol.43 (1), p.104-106

1997

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Biotin supplementation increases expression of genes encoding interferon-gamma, interleukin-1beta, and 3-methylcrotonyl-CoA carboxylase, and decreases expression of the gene encoding interleukin-4 in human peripheral blood mononuclear cells

The Journal of nutrition, 2003-03, Vol.133 (3), p.716-719

2003

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The Construction of a Yeast Artificial Chromosome (YAC) Contig in the Vicinity of the Usher Syndrome Type IIa (USH2A) Gene in 1q41

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.79-86

1996

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Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

Genetics in medicine, 2019-04, Vol.21 (4), p.948-954

2019

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Genome-wide mutation avalanches induced in diploid yeast cells by a base analog or an APOBEC deaminase

Targeted myocardial gene expression in failing hearts by RNA sequencing

Telomerase-immortalized human mammary stem/progenitor cells with ability to self-renew and differentiate

Genome-wide expression profiling reveals transcriptomic variation and perturbed gene networks in androgen-dependent and androgen-independent prostate cancer cells

ATM, CTLA4, MNDA, and HEM1 in High versus Low CD38–Expressing B-Cell Chronic Lymphocytic Leukemia

Attachment-regulated signaling networks in the fibroblast-populated 3D collagen matrix

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations

Molecular basis of environmentally induced birth defects

Identification of two putative novel folate receptor genes in humans and mouse

Distinct gene expression profiles in different B-cell compartments in human peripheral lymphoid organs

Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa

Casodex treatment induces hypoxia-related gene expression in the LNCaP prostate cancer progression model

Biotin Supplementation Increases Expression of Genes Encoding Interferon-γ, Interleukin-1β, and 3-Methylcrotonyl-CoA Carboxylase, and Decreases Expression of the Gene Encoding Interleukin-4 in Human Peripheral Blood Mononuclear Cells

Identification and Characterization of the Human and Mouse SLC19A3 Gene: A Novel Member of the Reduced Folate Family of Micronutrient Transporter Genes

18q22.3 → 18q23 deletion syndrome and cleft palate

Isolation of a Gene Encoding a Novel Member of the Nuclear Receptor Superfamily from the Critical Region of Usher Syndrome Type IIa at 1q41

Identification of the Mouse and Rat Orthologs of the Gene Mutated in Usher Syndrome Type IIA and the Cellular Source of USH2A mRNA in Retina, a Target Tissue of the Disease

Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32

Biotin supplementation increases expression of genes encoding interferon-gamma, interleukin-1beta, and 3-methylcrotonyl-CoA carboxylase, and decreases expression of the gene encoding interleukin-4 in human peripheral blood mononuclear cells

The Construction of a Yeast Artificial Chromosome (YAC) Contig in the Vicinity of the Usher Syndrome Type IIa (USH2A) Gene in 1q41

Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37

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