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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 1, 1996
Surface adhesion-mediated regulation of chondrocyte-specific gene expression in the nontransformed RCJ 3.1C5.18 rat chondrocyte cell line
S McDougall, Y H Fu, G N Lowe, et al.
Science (New York, N.Y.)
|
March 16, 1992
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
Y H Fu, A Pizzuti, R G Fenwick, et al.
Science (New York, N.Y.)
|
April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
Y H Fu, D L Friedman, S Richards, et al.
Human Molecular Genetics
|
December 6, 2001
Association of ataxin-7 with the proteasome subunit S4 of the 19S regulatory complex
A Matilla, C Gorbea, D D Einum, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
June 1, 2022
[Prediction on the cardio-cerebrovascular death and probability of premature death caused by common risk factors in China in 2030]
Z Z Rao, Y H Fu, R T Li, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
February 7, 2022
[Prediction of disease burden caused by malignant cancer in the context of risk factor control in China, 2030]
Y H Fu, Z Z Rao, R T Li, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
February 20, 2022
[Prediction on the burden of disease of chronic obstructive pulmonary disease and simulation of the effectiveness of controlling risk factors in China by 2030]
R T Li, Z Z Rao, Y H Fu, et al.
Cell
|
May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
A J Verkerk, M Pieretti, J S Sutcliffe, et al.
Cell
|
December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
American Journal of Human Genetics
|
February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group
C E Yu, J Oshima, E M Wijsman, et al.
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Search research articles
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Showing results (71-80 of 94) with videos related to
Sort By:
Page
of 10
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 1, 1996
Surface adhesion-mediated regulation of chondrocyte-specific gene expression in the nontransformed RCJ 3.1C5.18 rat chondrocyte cell line
S McDougall, Y H Fu, G N Lowe, et al.
Science (New York, N.Y.)
|
March 16, 1992
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
Y H Fu, A Pizzuti, R G Fenwick, et al.
Science (New York, N.Y.)
|
April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy
Y H Fu, D L Friedman, S Richards, et al.
Human Molecular Genetics
|
December 6, 2001
Association of ataxin-7 with the proteasome subunit S4 of the 19S regulatory complex
A Matilla, C Gorbea, D D Einum, et al.
Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine]
|
June 1, 2022
[Prediction on the cardio-cerebrovascular death and probability of premature death caused by common risk factors in China in 2030]
Z Z Rao, Y H Fu, R T Li, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
February 7, 2022
[Prediction of disease burden caused by malignant cancer in the context of risk factor control in China, 2030]
Y H Fu, Z Z Rao, R T Li, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi
|
February 20, 2022
[Prediction on the burden of disease of chronic obstructive pulmonary disease and simulation of the effectiveness of controlling risk factors in China by 2030]
R T Li, Z Z Rao, Y H Fu, et al.
Cell
|
May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
A J Verkerk, M Pieretti, J S Sutcliffe, et al.
Cell
|
December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
Y H Fu, D P Kuhl, A Pizzuti, et al.
American Journal of Human Genetics
|
February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group
C E Yu, J Oshima, E M Wijsman, et al.
Page
of 10