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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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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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Microarray Analysis of Paramecium bursaria Chlorella Virus 1 Transcription

Journal of Virology, 2010-01, Vol.84 (1), p.532-542

2010

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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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Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complex

BMC genomics, 2008-04, Vol.9 (1), p.156-156

2008

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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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Genome-Wide Gene Expression in relation to Age in Large Laboratory Cohorts of Drosophila melanogaster

Genetics Research International, 2015-01, Vol.2015, p.835624-19

2015

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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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MUC4, a multifunctional transmembrane glycoprotein, induces oncogenic transformation of NIH3T3 mouse fibroblast cells

Cancer research (Chicago, Ill.), 2008-11, Vol.68 (22), p.9231-9238

2008

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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

2004

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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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The Canonical Wnt Pathway Regulates Retinal Stem Cells/Progenitors in Concert with Notch Signaling

Developmental neuroscience, 2008-01, Vol.30 (6), p.389-409

2008

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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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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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Response to correspondence on "Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation"

Genome Biology, 2021-04, Vol.22 (1), p.99-99, Article 99

2021

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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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Genome-Wide Mutation Avalanches Induced in Diploid Yeast Cells by a Base Analog or an APOBEC Deaminase: e1003736

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

2013

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18q22.3 RT 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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Biotin supplementation increases expression of genes encoding interferon-(gamma), interleukin-1(beta), and 3-methylcrotonyl-CoA carboxylase, and decreases expression of teh gene encoding interleukin-4 in human peripheral blood mononuclear cells

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

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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18q22.3 --> 18q23 deletion syndrome and cleft palate

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

2010

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Genetic Variants in Circadian Rhythm Genes and Self-Reported Sleep Quality in Women with Breast Cancer

Journal of circadian rhythms, 2019-07, Vol.17 (1), p.6-6

2019

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Automated Apnea-Hypopnea Index from Oximetry and Spectral Analysis of Cardiopulmonary Coupling

Annals of the American Thoracic Society, 2021-05, Vol.18 (5), p.876-883

2021

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1 – 25 von 26

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

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

Microarray Analysis of Paramecium bursaria Chlorella Virus 1 Transcription

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

Microarray analysis of E9.5 reduced folate carrier (RFC1; Slc19a1) knockout embryos reveals altered expression of genes in the cubilin-megalin multiligand endocytic receptor complex

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

Genome-Wide Gene Expression in relation to Age in Large Laboratory Cohorts of Drosophila melanogaster

Molecular basis of environmentally induced birth defects

MUC4, a multifunctional transmembrane glycoprotein, induces oncogenic transformation of NIH3T3 mouse fibroblast cells

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

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 Canonical Wnt Pathway Regulates Retinal Stem Cells/Progenitors in Concert with Notch Signaling

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

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

Response to correspondence on "Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation"

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

Genome-Wide Mutation Avalanches Induced in Diploid Yeast Cells by a Base Analog or an APOBEC Deaminase: e1003736

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

Biotin supplementation increases expression of genes encoding interferon-(gamma), interleukin-1(beta), and 3-methylcrotonyl-CoA carboxylase, and decreases expression of teh 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

18q22.3 --> 18q23 deletion syndrome and cleft palate

Genetic Variants in Circadian Rhythm Genes and Self-Reported Sleep Quality in Women with Breast Cancer

Automated Apnea-Hypopnea Index from Oximetry and Spectral Analysis of Cardiopulmonary Coupling

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