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Genomics
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October 29, 1998
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region
F M Hisama, J Oshima, C E Yu, et al.
Molecular Syndromology
|
October 30, 2010
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features
B Saha, D Lessel, F M Hisama, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2002
Atypical progeroid syndrome: an unknown helicase gene defect?
M W G Ruijs, R N J van Andel, J Oshima, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
May 29, 2004
Usefulness of switching to cabergoline from other dopamine agonists in patients with advanced Parkinson's disease
M Shiraishi, T Kamo, M Hotta, et al.
Human Genetics
|
December 24, 1997
An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants
C E Ogburn, J Oshima, M Poot, et al.
American Journal of Human Genetics
|
August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome
C E Yu, J Oshima, K A Goddard, et al.
Nature Genetics
|
September 1, 1997
The Werner syndrome protein is a DNA helicase
M D Gray, J C Shen, A S Kamath-Loeb, et al.
American Journal of Human Genetics
|
June 1, 1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers
K A Goddard, C E Yu, J Oshima, et al.
Cancer Research
|
May 16, 2000
Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes
M J Moser, W L Bigbee, S G Grant, et al.
Human Genetics
|
May 1, 1994
Evidence against DNA polymerase beta as a candidate gene for Werner syndrome
M Chang, G C Burmer, J Sweasy, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 61) with videos related to
Sort By:
Page
of 7
Genomics
|
October 29, 1998
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region
F M Hisama, J Oshima, C E Yu, et al.
Molecular Syndromology
|
October 30, 2010
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features
B Saha, D Lessel, F M Hisama, et al.
American Journal of Medical Genetics. Part A
|
December 28, 2002
Atypical progeroid syndrome: an unknown helicase gene defect?
M W G Ruijs, R N J van Andel, J Oshima, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
May 29, 2004
Usefulness of switching to cabergoline from other dopamine agonists in patients with advanced Parkinson's disease
M Shiraishi, T Kamo, M Hotta, et al.
Human Genetics
|
December 24, 1997
An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants
C E Ogburn, J Oshima, M Poot, et al.
American Journal of Human Genetics
|
August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome
C E Yu, J Oshima, K A Goddard, et al.
Nature Genetics
|
September 1, 1997
The Werner syndrome protein is a DNA helicase
M D Gray, J C Shen, A S Kamath-Loeb, et al.
American Journal of Human Genetics
|
June 1, 1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers
K A Goddard, C E Yu, J Oshima, et al.
Cancer Research
|
May 16, 2000
Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes
M J Moser, W L Bigbee, S G Grant, et al.
Human Genetics
|
May 1, 1994
Evidence against DNA polymerase beta as a candidate gene for Werner syndrome
M Chang, G C Burmer, J Sweasy, et al.
Page
of 7