Rachel Wevrick - AILBRY - Article Search

Results for 'Rachel Wevrick' :

Identification of a novel paternally expressed gene in the Prader - Willi syndrome region

Publication Year: 1994

DOI: https://doi.org/10.1093/hmg/3.10.1877

Abstract:

Authors:
- Rachel Wevrick
- Julie A. Kerns
- Uta Francke
Cloning and analysis of the murine Fanconi anemia group C cDNA

Publication Year: 1993

DOI: https://doi.org/10.1093/hmg/2.6.655

Abstract:

Authors:
- Rachel Wevrick
- C. Clarke
- Manuel Buchwald
Genomic disorders : the genomic basis of disease

Publication Year: 2006

DOI: DOI not available

Abstract:

Authors:
- James R. Lupski
- Paweł Stankiewicz
Variation in electrical resistance along length of rat proximal convoluted tubule

Publication Year: 1973

DOI: https://doi.org/10.1152/ajplegacy.1973.225.1.48

Abstract:

Authors:
- JF Seely
Energy homeostasis in Prader–Willi Syndrome: How clinical research informs studies of animal models of genetic obesity

Publication Year: 2012

DOI: https://doi.org/10.1002/ajmg.a.35249

Abstract:

Authors:
- Rebecca E. Mercer
- Rachel Wevrick
Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

Publication Year: 1994

DOI: https://doi.org/10.1016/0092-8674(94)90528-2

Abstract:

Authors:
- Jonathan M.J. Derry
- Hans D. Ochs
- Uta Francke
Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes

Publication Year: 2001

DOI: https://doi.org/10.1146/annurev.genom.2.1.153

Abstract:

Authors:
- Robert D. Nicholls
- Jessica L. Knepper
Zac1 (Lot1), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines

Publication Year: 2000

DOI: https://doi.org/10.1128/mcb.20.9.3308-3315.2000

Abstract:

Authors:
- Graziella Piras
- Aboubaker El Kharroubi
- Serguei Kozlov
- Diana Escalante‐Alcalde
- Lídia Hernandez
- Neal G. Copeland
- Debra J. Gilbert
- Nancy A. Jenkins
- Colin L. Stewart
Isolation of a Ubiquitin-like (UBL5) Gene from a Screen Identifying Highly Expressed and Conserved Iris Genes

Publication Year: 2001

DOI: https://doi.org/10.1006/geno.2000.6439

Abstract:

Authors:
- James S. Friedman
- Ben F. Koop
- Vincent Raymond
- Michael A. Walter
β satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes

Publication Year: 1992

DOI: https://doi.org/10.1016/0888-7543(92)90450-7

Abstract:

Authors:
- Gillian Greig
- Huntington F. Willard
Integration of human α-satellite DNA into simian chromosomes: Centromere protein binding and disruption of normal chromosome segregation

Publication Year: 1992

DOI: https://doi.org/10.1016/0092-8674(92)90436-g

Abstract:

Authors:
- Thomas Haaf
- Peter E. Warburton
- Huntington F. Willard
Cellular and disease functions of the Prader–Willi Syndrome geneMAGEL2

Publication Year: 2017

DOI: https://doi.org/10.1042/bcj20160616

Abstract:

Authors:
- Klementina Fon Tacer
- Patrick Ryan Potts
A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23

Publication Year: 2000

DOI: https://doi.org/10.1086/302722

Abstract:

Authors:
- Risa Peoples
- Yvonne Franke
- Yu-Ker Wang
- Luís A. Pérez-Jurado
- Tamar Paperna
- Michael J. Cisco
- Uta Francke
Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

Publication Year: 1997

DOI: https://doi.org/10.1086/513894

Abstract:

Authors:
- Farideh Mirzayans
- Alan J. Mears
- Sun-Wei Guo
- W G Pearce
- Michael A. Walter
Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation

Publication Year: 2018

DOI: https://doi.org/10.1167/iovs.18-24301

Abstract:

Authors:
- Kumari Alka
- Joseph R. Casey

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AILBRY - Article Search

Results for 'Rachel Wevrick' :

Identification of a novel paternally expressed gene in the Prader - Willi syndrome region

Cloning and analysis of the murine Fanconi anemia group C cDNA

Genomic disorders : the genomic basis of disease

Variation in electrical resistance along length of rat proximal convoluted tubule

Energy homeostasis in Prader–Willi Syndrome: How clinical research informs studies of animal models of genetic obesity

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes

<i>Zac1</i> (<i>Lot1</i>), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines

Isolation of a Ubiquitin-like (UBL5) Gene from a Screen Identifying Highly Expressed and Conserved Iris Genes

β satellite DNA: Characterization and localization of two subfamilies from the distal and proximal short arms of the human acrocentric chromosomes

Integration of human α-satellite DNA into simian chromosomes: Centromere protein binding and disruption of normal chromosome segregation

Cellular and disease functions of the Prader–Willi Syndrome gene<i>MAGEL2</i>

A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23

Identification of the Human Chromosomal Region Containing the Iridogoniodysgenesis Anomaly Locus by Genomic-Mismatch Scanning

Ophthalmic Nonsteroidal Anti-Inflammatory Drugs as a Therapy for Corneal Dystrophies Caused by SLC4A11 Mutation

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