Search research articles
Contact Us
Filters
Showing results (961-970 of 990) with videos related to
Page
of 99
Sort By:
American Journal of Medical Genetics
|
September 20, 1996
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease
K Endo, H Sasaki, A Wakisaka, et al.
Nature Genetics
|
February 14, 1998
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch
S Igarashi, R Koide, T Shimohata, et al.
Neuron
|
February 17, 2000
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA
G Schilling, J D Wood, K Duan, et al.
Neurology
|
February 1, 1997
Machado-Joseph disease in four Chinese pedigrees: molecular analysis of 15 patients including two juvenile cases and clinical correlations
Y X Zhou, Y Takiyama, S Igarashi, et al.
American Journal of Human Genetics
|
October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
H Takano, G Cancel, T Ikeuchi, et al.
Neurogenetics
|
March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity
M A Pericak-Vance, M C Speer, F Lennon, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 14, 1998
Clinical features of ovarian cancer in Japanese women with germ-line mutations of BRCA1
H Aida, K Takakuwa, H Nagata, et al.
Neurology
|
May 12, 2004
Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5
H Ohtake, T Shimohata, K Terajima, et al.
Lupus
|
February 14, 2019
Complete renal response at 12 months after induction therapy is associated with renal relapse-free rate in lupus nephritis: a single-center, retrospective cohort study
K Ichinose, M Kitamura, S Sato, et al.
Nature Genetics
|
October 5, 2001
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
H Date, O Onodera, H Tanaka, et al.
Page
of 99
Search research articles
Search
Showing results (961-970 of 990) with videos related to
Sort By:
Page
of 99
American Journal of Medical Genetics
|
September 20, 1996
Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease
K Endo, H Sasaki, A Wakisaka, et al.
Nature Genetics
|
February 14, 1998
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch
S Igarashi, R Koide, T Shimohata, et al.
Neuron
|
February 17, 2000
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA
G Schilling, J D Wood, K Duan, et al.
Neurology
|
February 1, 1997
Machado-Joseph disease in four Chinese pedigrees: molecular analysis of 15 patients including two juvenile cases and clinical correlations
Y X Zhou, Y Takiyama, S Igarashi, et al.
American Journal of Human Genetics
|
October 3, 1998
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
H Takano, G Cancel, T Ikeuchi, et al.
Neurogenetics
|
March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity
M A Pericak-Vance, M C Speer, F Lennon, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
May 14, 1998
Clinical features of ovarian cancer in Japanese women with germ-line mutations of BRCA1
H Aida, K Takakuwa, H Nagata, et al.
Neurology
|
May 12, 2004
Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5
H Ohtake, T Shimohata, K Terajima, et al.
Lupus
|
February 14, 2019
Complete renal response at 12 months after induction therapy is associated with renal relapse-free rate in lupus nephritis: a single-center, retrospective cohort study
K Ichinose, M Kitamura, S Sato, et al.
Nature Genetics
|
October 5, 2001
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
H Date, O Onodera, H Tanaka, et al.
Page
of 99