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Prader-Willi Syndrome Is Caused by Disruption of the SNRPN Gene

American journal of human genetics, 1999, Vol.64 (1), p.70-76

1999

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Who are the Okinawans? Ancestry, genome diversity, and implications for the genetic study of human longevity from a geographically isolated population

The journals of gerontology. Series A, Biological sciences and medical sciences, 2014-12, Vol.69 (12), p.1474-1484

2014

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Correlation between growth control, neoplastic potential and endogenous connexin43 expression in HeLa cell lines: implications for tumor progression

Carcinogenesis (New York), 2000-02, Vol.21 (2), p.311-315

2000

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A Prospective Study of High-Density Lipoprotein Cholesterol, Cholesteryl Ester Transfer Protein Gene Variants, and Healthy Aging in Very Old Japanese-American Men

The journals of gerontology. Series A, Biological sciences and medical sciences, 2008-11, Vol.63 (11), p.1235-1240

2008

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Detection of bcr-abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization

Science (American Association for the Advancement of Science), 1990-10, Vol.250 (4980), p.559-562

1990

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Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes

Human genetics, 1988-12, Vol.80 (4), p.322-328

DONLON, T. A

1988

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Case-Control Study of Ovarian Cancer and Polymorphisms in Genes Involved in Catecholestrogen Formation and Metabolism

Cancer epidemiology, biomarkers & prevention, 2001-03, Vol.10 (3), p.209-216

2001

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Isolation of Molecular Probes Associated with the Chromosome 15 Instability in the Prader--Willi Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1986-06, Vol.83 (12), p.4408-4412

1986

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CYP17 genotype and ovarian cancer : A null case-control study

Cancer epidemiology, biomarkers & prevention, 2001-05, Vol.10 (5), p.563-564

2001

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Association of Methylenetetrahydrofolate Reductase Polymorphism C677T and Dietary Folate with the Risk of Cervical Dysplasia

Cancer epidemiology, biomarkers & prevention, 2001-12, Vol.10 (12), p.1275-1280

2001

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Importance of bone marrow cytogenetic evaluation before autologous bone marrow transplantation for Hodgkin's disease

Journal of clinical oncology, 1991-09, Vol.9 (9), p.1575-1579

1991

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Human Von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4706), p.1401-1406

1985

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Enhanced Detection of the t(14;18) Translocation in Malignant Lymphoma Using Pulsed-Field Gel Electrophoresis

Blood, 1991-09, Vol.78 (6), p.1552-1560

1991

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Induction of proliferation of human follicular (B type) lymphoma cells by cognate interaction with CD4+ T cell clones

The Journal of immunology (1950), 1990-04, Vol.144 (7), p.2550-2557

1990

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Determination of the breakpoint of the common α‐thalassaemia deletion in Filipinos in Hawaii

British journal of haematology, 1999-02, Vol.104 (2), p.284-287

1999

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FOXO3 gene variants and human aging: coding variants may not be key players

The journals of gerontology. Series A, Biological sciences and medical sciences, 2012-11, Vol.67 (11), p.1132-1139

2012

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Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12

Genomics (San Diego, Calif.), 1990-03, Vol.6 (3), p.548-553

1990

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Erratum to: Minimal shortening of leukocyte telomere length across age groups in a cross-sectional study for carriers of a longevity-associated FOXO3 allele

The journals of gerontology. Series A, Biological sciences and medical sciences, 2019-01, Vol.74 (2), p.192-192

2019

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Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands

Human genetics, 1983-01, Vol.65 (2), p.144-146

1983

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Genetic analysis of TOR complex gene variation with human longevity: a nested case-control study of American men of Japanese ancestry

The journals of gerontology. Series A, Biological sciences and medical sciences, 2015-02, Vol.70 (2), p.133-142

2015

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Association analyses of insulin signaling pathway gene polymorphisms with healthy aging and longevity in Americans of Japanese ancestry

The journals of gerontology. Series A, Biological sciences and medical sciences, 2014-03, Vol.69 (3), p.270-273

2014

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Localization of the Gene Encoding the Human Interleukin-2 Receptor on Chromosome 10

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4707), p.1547-1549

1985

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Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2

Brain research, 1986-12, Vol.1 (3), p.271-280

1986

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Expression of bcr-abl fusion transcripts following bone marrow transplantation for Philadelphia chromosome-positive leukemia

Leukemia, 1990-08, Vol.4 (8), p.541-547

1990

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Deletion mapping of DNA segments from the Y chromosome long arm and their analysis in an XX male

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.51-56

1991

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Prader-Willi Syndrome Is Caused by Disruption of the SNRPN Gene

Who are the Okinawans? Ancestry, genome diversity, and implications for the genetic study of human longevity from a geographically isolated population

Correlation between growth control, neoplastic potential and endogenous connexin43 expression in HeLa cell lines: implications for tumor progression

A Prospective Study of High-Density Lipoprotein Cholesterol, Cholesteryl Ester Transfer Protein Gene Variants, and Healthy Aging in Very Old Japanese-American Men

Detection of bcr-abl Fusion in Chronic Myelogeneous Leukemia by in Situ Hybridization

Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes

Case-Control Study of Ovarian Cancer and Polymorphisms in Genes Involved in Catecholestrogen Formation and Metabolism

Isolation of Molecular Probes Associated with the Chromosome 15 Instability in the Prader--Willi Syndrome

CYP17 genotype and ovarian cancer : A null case-control study

Association of Methylenetetrahydrofolate Reductase Polymorphism C677T and Dietary Folate with the Risk of Cervical Dysplasia

Importance of bone marrow cytogenetic evaluation before autologous bone marrow transplantation for Hodgkin's disease

Human Von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization

Enhanced Detection of the t(14;18) Translocation in Malignant Lymphoma Using Pulsed-Field Gel Electrophoresis

Induction of proliferation of human follicular (B type) lymphoma cells by cognate interaction with CD4+ T cell clones

Determination of the breakpoint of the common α‐thalassaemia deletion in Filipinos in Hawaii

FOXO3 gene variants and human aging: coding variants may not be key players

Localization of a human T-cell-specific gene, RANTES (D17S136E), to chromosome 17q11.2-q12

Erratum to: Minimal shortening of leukocyte telomere length across age groups in a cross-sectional study for carriers of a longevity-associated FOXO3 allele

Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands

Genetic analysis of TOR complex gene variation with human longevity: a nested case-control study of American men of Japanese ancestry

Association analyses of insulin signaling pathway gene polymorphisms with healthy aging and longevity in Americans of Japanese ancestry

Localization of the Gene Encoding the Human Interleukin-2 Receptor on Chromosome 10

Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2

Expression of bcr-abl fusion transcripts following bone marrow transplantation for Philadelphia chromosome-positive leukemia

Deletion mapping of DNA segments from the Y chromosome long arm and their analysis in an XX male

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