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The Journal of Biological Chemistry
|
December 5, 2000
A new member of the HCO3(-) transporter superfamily is an apical anion exchanger of beta-intercalated cells in the kidney
H Tsuganezawa, K Kobayashi, M Iyori, et al.
Leukemia
|
January 19, 2017
Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia
N Yoshida, H Sakaguchi, H Muramatsu, et al.
Transplantation Proceedings
|
June 15, 2004
Characteristics of pancreas transplantation currently performed in japan
M Ishibashi, T Ito, A Sugitani, et al.
American Journal of Human Genetics
|
November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy
S Gobin-Limballe, F Djouadi, F Aubey, et al.
Human Mutation
|
October 29, 1998
Ataxia-telangiectasia in the Japanese population: identification of R1917X, W2491R, R2909G, IVS33+2T-->A, and 7883del5, the latter two being relatively common mutations
T Fukao, X Q Song, T Yoshida, et al.
Genomics
|
August 31, 2000
Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations
T Fukao, G A Mitchell, X Q Song, et al.
Genomics
|
July 1, 1996
Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene
I Pecker, K B Avraham, D J Gilbert, et al.
Journal of Investigational Allergology & Clinical Immunology
|
April 27, 2012
Risk factors for infantile atopic dermatitis and recurrent wheezing
N Kawamoto, T Fukao, H Kaneko, et al.
Journal of Medical Genetics
|
June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family
J Dai, O-H Kim, T-J Cho, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 139) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 139 results.
The Journal of Biological Chemistry
|
December 5, 2000
A new member of the HCO3(-) transporter superfamily is an apical anion exchanger of beta-intercalated cells in the kidney
H Tsuganezawa, K Kobayashi, M Iyori, et al.
Leukemia
|
January 19, 2017
Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia
N Yoshida, H Sakaguchi, H Muramatsu, et al.
Transplantation Proceedings
|
June 15, 2004
Characteristics of pancreas transplantation currently performed in japan
M Ishibashi, T Ito, A Sugitani, et al.
American Journal of Human Genetics
|
November 14, 2007
Genetic basis for correction of very-long-chain acyl-coenzyme A dehydrogenase deficiency by bezafibrate in patient fibroblasts: toward a genotype-based therapy
S Gobin-Limballe, F Djouadi, F Aubey, et al.
Human Mutation
|
October 29, 1998
Ataxia-telangiectasia in the Japanese population: identification of R1917X, W2491R, R2909G, IVS33+2T-->A, and 7883del5, the latter two being relatively common mutations
T Fukao, X Q Song, T Yoshida, et al.
Genomics
|
August 31, 2000
Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations
T Fukao, G A Mitchell, X Q Song, et al.
Genomics
|
July 1, 1996
Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene
I Pecker, K B Avraham, D J Gilbert, et al.
Journal of Investigational Allergology & Clinical Immunology
|
April 27, 2012
Risk factors for infantile atopic dermatitis and recurrent wheezing
N Kawamoto, T Fukao, H Kaneko, et al.
Journal of Medical Genetics
|
June 26, 2010
Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family
J Dai, O-H Kim, T-J Cho, et al.
Page
of 14