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S9 Current knowledge on genetic predispositions for breast cancer

Breast (Edinburgh), 2009, Vol.18, p.S4-S4

Brody, L.C

2009

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A founder mutation in LEPRE1 causes lethal recessive type VIII osteogenesis imperfecta and occurs in West Africans and African Americans

Bone (New York, N.Y.), 2010-06, Vol.47, p.S152-S152

2010

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Genome‐wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance

Journal of thrombosis and haemostasis, 2016-09, Vol.14 (9), p.1888-1898

2016

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Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences

The Journal of biological chemistry, 1992-02, Vol.267 (5), p.3302-3307

1992

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Genetic and nutritional deficiencies in folate metabolism influence tumorigenicity in Apc(min/+) mice

The Journal of nutritional biochemistry, 2007-05, Vol.18, p.305-312

2007

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Considerations for Designing a Prototype Genetic Test for Use in Translational Research

Public health genomics, 2010-01, Vol.13 (3), p.155-165

2010

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BRCA1 mutations in African Americans

Human genetics, 1999-07, Vol.105 (1-2), p.28-31

1999

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A Response to ‘Why Realistic Test Scenarios in Translational Research Remain Hypothetical’

Public health genomics, 2010-02, Vol.13 (3), p.169-170

2010

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Splice-Mediated Insertion of an Alu Sequence Inactivates Ornithine δ-Aminotransferase: A Role for Alu Elements in Human Mutation

Proceedings of the National Academy of Sciences - PNAS, 1991-02, Vol.88 (3), p.815-819

1991

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Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17

Genomics (San Diego, Calif.), 1995, Vol.25 (1), p.238-247

1995

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407-2 Characterization of a Recombination Event Excluding the Harvey-ras-1 (H-ras-1) Locus in a Romano-Ward Long QT Syndrome Family Linked to Chromosome 11p15 and Isolation of a Polymorphic Repeat Telomeric to H-ras-1

Journal of the American College of Cardiology, 1995-02, Vol.25 (2), p.1A-1A

1995

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BRCA1 mutations in African Americans

Human genetics, 1999-08, Vol.105 (1-2), p.28-31

1999

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The Isolation of cDNAs from OATL1 at Xp11.2 Using a 480-kb YAC

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.440-446

1993

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A YAC-, P1-, and cosmid-based physical Map of the BRCA1 region on chromosome 17q21

Genomics (San Diego, Calif.), 1995, Vol.25 (1), p.264-273

1995

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Localization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21

Genomics (San Diego, Calif.), 1994-05, Vol.21 (2), p.444-446

1994

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Progress toward isolation of a breast cancer susceptibility gene, BRCA1

Cold Spring Harbor Symposia on Quantitative Biology, 1994, Vol.59, p.531-536

1994

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Detection of heterozygous mutations in brca1 using high density oligonucleotide arrays and two-color fluorescence analysis

Cancer genetics and cytogenetics, 1997-10, Vol.98 (2), p.155-155

1997

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Southern Foresters' Perceptions of Climate Change: Implications for Educational Program Development

Journal of extension, 2016-12, Vol.54 (6)

2016

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Sibling structure and parental sex-typing of children's household tasks

Journal of marriage and family, 1985-05, Vol.47 (2), p.265-273

1985

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1212 - PRIMARY SITES OF DRUG ACTION INVOLVED IN DIGOXIN-INDUCED ALTERATIONS IN SYMPATHETIC AND PHRENIC NERVE ACTIVITY

Abstracts: Sixth International Congress of Pharmacology, 1977, p.507-507

1977

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S9 Current knowledge on genetic predispositions for breast cancer

A founder mutation in LEPRE1 causes lethal recessive type VIII osteogenesis imperfecta and occurs in West Africans and African Americans

Genome‐wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance

Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequences

Genetic and nutritional deficiencies in folate metabolism influence tumorigenicity in Apc(min/+) mice

Considerations for Designing a Prototype Genetic Test for Use in Translational Research

BRCA1 mutations in African Americans

A Response to ‘Why Realistic Test Scenarios in Translational Research Remain Hypothetical’

Splice-Mediated Insertion of an Alu Sequence Inactivates Ornithine δ-Aminotransferase: A Role for Alu Elements in Human Mutation

Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17

407-2 Characterization of a Recombination Event Excluding the Harvey-ras-1 (H-ras-1) Locus in a Romano-Ward Long QT Syndrome Family Linked to Chromosome 11p15 and Isolation of a Polymorphic Repeat Telomeric to H-ras-1

BRCA1 mutations in African Americans

The Isolation of cDNAs from OATL1 at Xp11.2 Using a 480-kb YAC

A YAC-, P1-, and cosmid-based physical Map of the BRCA1 region on chromosome 17q21

Localization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21

Progress toward isolation of a breast cancer susceptibility gene, BRCA1

Detection of heterozygous mutations in brca1 using high density oligonucleotide arrays and two-color fluorescence analysis

Southern Foresters' Perceptions of Climate Change: Implications for Educational Program Development

Sibling structure and parental sex-typing of children's household tasks

1212 - PRIMARY SITES OF DRUG ACTION INVOLVED IN DIGOXIN-INDUCED ALTERATIONS IN SYMPATHETIC AND PHRENIC NERVE ACTIVITY

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