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Journal of Medical Genetics
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October 25, 2008
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA
S Farasat, M-H Wei, M Herman, et al.
Genomics
|
June 1, 1992
A genetic linkage map of 96 loci on the short arm of human chromosome 3
K Tory, F Latif, W Modi, et al.
Genomics
|
February 13, 2001
PANORAMA: an integrated Web-based sequence analysis tool and its role in gene discovery
A Pertsemlidis, A Pande, B Miller, et al.
Human Genetics
|
November 3, 1998
In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion molecules
M H Wei, I Karavanova, S V Ivanov, et al.
Nature Genetics
|
May 1, 1994
Mutations of the VHL tumour suppressor gene in renal carcinoma
J R Gnarra, K Tory, Y Weng, et al.
Oncogene
|
July 22, 1998
Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene
Y Sekido, M Ahmadian, I I Wistuba, et al.
Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]
|
March 1, 1987
[Localization of oncoprotein P21ras in the human liver cancer]
J X Hong, M H Wei, X Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 30, 1996
Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns
Y Sekido, S Bader, F Latif, et al.
The Journal of Biological Chemistry
|
April 15, 2000
Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2)
B Gao, Y Sekido, A Maximov, et al.
Indian Journal of Cancer
|
March 31, 2015
A retrospective clinical study of bevacizumab combined with gemcibabine or paclitaxel in the treatment of recurrent ovarian cancer
M D Wu, Y Wang, T Ding, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Journal of Medical Genetics
|
October 25, 2008
Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA
S Farasat, M-H Wei, M Herman, et al.
Genomics
|
June 1, 1992
A genetic linkage map of 96 loci on the short arm of human chromosome 3
K Tory, F Latif, W Modi, et al.
Genomics
|
February 13, 2001
PANORAMA: an integrated Web-based sequence analysis tool and its role in gene discovery
A Pertsemlidis, A Pande, B Miller, et al.
Human Genetics
|
November 3, 1998
In silico-initiated cloning and molecular characterization of a novel human member of the L1 gene family of neural cell adhesion molecules
M H Wei, I Karavanova, S V Ivanov, et al.
Nature Genetics
|
May 1, 1994
Mutations of the VHL tumour suppressor gene in renal carcinoma
J R Gnarra, K Tory, Y Weng, et al.
Oncogene
|
July 22, 1998
Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene
Y Sekido, M Ahmadian, I I Wistuba, et al.
Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]
|
March 1, 1987
[Localization of oncoprotein P21ras in the human liver cancer]
J X Hong, M H Wei, X Zhang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 30, 1996
Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patterns
Y Sekido, S Bader, F Latif, et al.
The Journal of Biological Chemistry
|
April 15, 2000
Functional properties of a new voltage-dependent calcium channel alpha(2)delta auxiliary subunit gene (CACNA2D2)
B Gao, Y Sekido, A Maximov, et al.
Indian Journal of Cancer
|
March 31, 2015
A retrospective clinical study of bevacizumab combined with gemcibabine or paclitaxel in the treatment of recurrent ovarian cancer
M D Wu, Y Wang, T Ding, et al.
Page
of 3