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Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice

Nature, 2003-10, Vol.425 (6959), p.721-727

2003

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Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes

Transgenic research, 2009-10, Vol.18 (5), p.769-785

2009

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A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice

PLoS genetics, 2013, Vol.9 (12), p.e1003967

2013

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Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line

Mammalian genome, 2007-08, Vol.18 (8), p.549-558

2007

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Rederivation of transgenic and gene-targeted mice by embryo transfer

Transgenic research, 2004-08, Vol.13 (4), p.363-371

2004

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Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.880-884

1987

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Resistance to organophosphorus agent toxicity in transgenic mice expressing the G117H mutant of human butyrylcholinesterase

Toxicology and applied pharmacology, 2004-05, Vol.196 (3), p.356-366

2004

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Isolation of human and murine homologues of the Drosophila minibrain gene : Human homologue maps to 21q22.2 in the Down syndrome critical region

Genomics (San Diego, Calif.), 1996-12, Vol.38 (3), p.331-339

1996

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Human chromosome 21-encoded cDNA clones

Gene, 1986, Vol.49 (3), p.361-369

1986

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Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance

Genome research, 1996-10, Vol.6 (10), p.1013

1996

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[30] Gel protein stains: Silver stain

Methods in Enzymology, 1984, Vol.104, p.441-447

1984

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Simplified silver protein detection and image enhancement methods in polyacrylamide gels

Electrophoresis, 1982-02, Vol.3 (1), p.17-23

1982

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Trace Polypeptides in Cellular Extracts and Human Body Fluids Detected by Two-Dimensional Electrophoresis and a Highly Sensitive Silver Stain

Proceedings of the National Academy of Sciences - PNAS, 1979-09, Vol.76 (9), p.4335-4339

1979

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Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.328-333

1996

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[17] Silver staining methods for polyacrylamide gel electrophoresis

Methods in Enzymology, 1983, Vol.96, p.230-239

1983

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Molecular Mechanism in the Formation of a Human Ring Chromosome 21

Proceedings of the National Academy of Sciences - PNAS, 1989-03, Vol.86 (6), p.1914-1918

1989

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Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2

Immunogenetics (New York), 1993-09, Vol.38 (6), p.387-399

1993

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Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3)

Human molecular genetics, 1995-12, Vol.4 (12), p.2347-2353

1995

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Isolation and Characterization of the Human and Mouse Homologues (SUPT4H andSupt4h) of the Yeast SPT4 Gene

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.368-375

1996

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MOLECULAR PROBES FOR HUMAN GENETIC DISEASES BY TWO-DIMENSIONAL PROTEIN ELECTROPHORESIS AND SILVER STAINING

Electrophoresis ‘82, 2019, p.327-342

2019

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Application of Molecular and Somatic Cell Genetics to the Study of Chromosome 21a

Annals of the New York Academy of Sciences, 1986-12, Vol.477 (1), p.151-159

1986

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Confirmation of assignment of the human α1-crystallin gene (CRYA1) to chromosome 21 with regional localization to q22.3

Human genetics, 1987-08, Vol.76 (4), p.375-380

1987

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Identification and Analysis of the Human and Murine Putative Chromatin Structure Regulator SUPT6H andSupt6h

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.328-333

1996

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Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody

Human genetics, 1986-09, Vol.74 (1), p.34-40

1986

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Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice

Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes

A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice

Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line

Rederivation of transgenic and gene-targeted mice by embryo transfer

Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

A novel intergenic ETnII-[beta] insertion mutation causes multiple malformations in Polypodia mice

Resistance to organophosphorus agent toxicity in transgenic mice expressing the G117H mutant of human butyrylcholinesterase

Isolation of human and murine homologues of the Drosophila minibrain gene : Human homologue maps to 21q22.2 in the Down syndrome critical region

Human chromosome 21-encoded cDNA clones

Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance

[30] Gel protein stains: Silver stain

Simplified silver protein detection and image enhancement methods in polyacrylamide gels

Trace Polypeptides in Cellular Extracts and Human Body Fluids Detected by Two-Dimensional Electrophoresis and a Highly Sensitive Silver Stain

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h

[17] Silver staining methods for polyacrylamide gel electrophoresis

Molecular Mechanism in the Formation of a Human Ring Chromosome 21

Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2

Identification of a novel gene, ETX1, from Xp21.1, a candidate gene for X-linked retinitis pigmentosa (RP3)

Isolation and Characterization of the Human and Mouse Homologues (SUPT4H andSupt4h) of the Yeast SPT4 Gene

MOLECULAR PROBES FOR HUMAN GENETIC DISEASES BY TWO-DIMENSIONAL PROTEIN ELECTROPHORESIS AND SILVER STAINING

Application of Molecular and Somatic Cell Genetics to the Study of Chromosome 21a

Confirmation of assignment of the human α1-crystallin gene (CRYA1) to chromosome 21 with regional localization to q22.3

Identification and Analysis of the Human and Murine Putative Chromatin Structure Regulator SUPT6H andSupt6h

Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody

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