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H X Deng

Showing results (31-40 of 61) with videos related to

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Journal of Biochemistry|July 1, 1992
A simple and efficient amplification method of DNA with unknown sequences and its application to microdissection/microcloningY Jinno, N Harada, K Yoshiura, et al.
Genomics|June 1, 1992
Microdissection of human chromosomal regions 8q23.3-q24.11 and 2q33-qter: construction of DNA libraries and isolation of their clonesT Hirota, K Tsukamoto, H X Deng, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Tropical Biomedicine|February 17, 2021
Survey of indoor sarcosaphagous insectsL P Ren, H X Deng, S Z Dong, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|July 16, 2008
Prokaryotic expression of a novel mouse pro-apoptosis protein PNAS-4 and application of its polyclonal antibodiesP Zhang, C T Wang, F Yan, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|February 9, 2000
[Molecular cloning of one splicing form of human M6b cDNA]J H Xia, C Y Liu, Q G Ruan, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Human Molecular Genetics|June 1, 1995
Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosisH X Deng, J A Tainer, H Mitsumoto, et al.
Nature|March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.
Science (New York, N.Y.)|August 20, 1993
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutaseH X Deng, A Hentati, J A Tainer, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Journal of Biochemistry|July 1, 1992
A simple and efficient amplification method of DNA with unknown sequences and its application to microdissection/microcloningY Jinno, N Harada, K Yoshiura, et al.
Genomics|June 1, 1992
Microdissection of human chromosomal regions 8q23.3-q24.11 and 2q33-qter: construction of DNA libraries and isolation of their clonesT Hirota, K Tsukamoto, H X Deng, et al.
Neurology|January 30, 2009
Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.
Tropical Biomedicine|February 17, 2021
Survey of indoor sarcosaphagous insectsL P Ren, H X Deng, S Z Dong, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|July 16, 2008
Prokaryotic expression of a novel mouse pro-apoptosis protein PNAS-4 and application of its polyclonal antibodiesP Zhang, C T Wang, F Yan, et al.
Yi Chuan Xue Bao = Acta Genetica Sinica|February 9, 2000
[Molecular cloning of one splicing form of human M6b cDNA]J H Xia, C Y Liu, Q G Ruan, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Human Molecular Genetics|June 1, 1995
Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosisH X Deng, J A Tainer, H Mitsumoto, et al.
Nature|March 4, 1993
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.
Science (New York, N.Y.)|August 20, 1993
Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutaseH X Deng, A Hentati, J A Tainer, et al.
Pageof 7