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Biochemical and Biophysical Research Communications
|
November 15, 1989
Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency
T Gotoda, M Senda, T Murase, et al.
Oral Diseases
|
November 25, 2003
Changes of alpha1-protease inhibitor and secretory leukocyte protease inhibitor levels in gingival crevicular fluid before and after non-surgical periodontal treatment
M Nakamura-Minami, Y Furuichi, K Ishikawa, et al.
Genomics
|
January 8, 1999
Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes
S Kitao, I Ohsugi, K Ichikawa, et al.
Cellular & Molecular Biology Research
|
January 1, 1993
Identification of specific intracellular domains of the human ETA receptor required for ligand binding and signal transduction
K Hashido, M Adachi, T Gamou, et al.
Nucleic Acids Research
|
June 20, 1998
Cloning and characterization of a human DEAH-box RNA helicase, a functional homolog of fission yeast Cdc28/Prp8
O Imamura, K Saiki, T Tani, et al.
The Journal of Biological Chemistry
|
June 25, 1981
Excess synthesis of viral mRNA 5-terminal oligonucleotides by reovirus transcriptase
M Yamakawa, Y Furuichi, K Nakashima, et al.
Molecular and Cellular Biology
|
October 17, 1998
Sp1-mediated transcription of the Werner helicase gene is modulated by Rb and p53
Y Yamabe, A Shimamoto, M Goto, et al.
Genomics
|
April 15, 1997
Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization
O Imamura, K Ichikawa, Y Yamabe, et al.
Nucleic Acids Research
|
May 11, 1989
Detection of familial LPL deficiency by PvuII RFLP
T Gotoda, M Senda, T Murase, et al.
American Journal of Medical Genetics
|
March 4, 2000
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
N M Lindor, Y Furuichi, S Kitao, et al.
Page
of 24
Search research articles
Search
Showing results (131-140 of 235) with videos related to
Sort By:
Page
of 24
Biochemical and Biophysical Research Communications
|
November 15, 1989
Gene polymorphism identified by PvuII in familial lipoprotein lipase deficiency
T Gotoda, M Senda, T Murase, et al.
Oral Diseases
|
November 25, 2003
Changes of alpha1-protease inhibitor and secretory leukocyte protease inhibitor levels in gingival crevicular fluid before and after non-surgical periodontal treatment
M Nakamura-Minami, Y Furuichi, K Ishikawa, et al.
Genomics
|
January 8, 1999
Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes
S Kitao, I Ohsugi, K Ichikawa, et al.
Cellular & Molecular Biology Research
|
January 1, 1993
Identification of specific intracellular domains of the human ETA receptor required for ligand binding and signal transduction
K Hashido, M Adachi, T Gamou, et al.
Nucleic Acids Research
|
June 20, 1998
Cloning and characterization of a human DEAH-box RNA helicase, a functional homolog of fission yeast Cdc28/Prp8
O Imamura, K Saiki, T Tani, et al.
The Journal of Biological Chemistry
|
June 25, 1981
Excess synthesis of viral mRNA 5-terminal oligonucleotides by reovirus transcriptase
M Yamakawa, Y Furuichi, K Nakashima, et al.
Molecular and Cellular Biology
|
October 17, 1998
Sp1-mediated transcription of the Werner helicase gene is modulated by Rb and p53
Y Yamabe, A Shimamoto, M Goto, et al.
Genomics
|
April 15, 1997
Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization
O Imamura, K Ichikawa, Y Yamabe, et al.
Nucleic Acids Research
|
May 11, 1989
Detection of familial LPL deficiency by PvuII RFLP
T Gotoda, M Senda, T Murase, et al.
American Journal of Medical Genetics
|
March 4, 2000
Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
N M Lindor, Y Furuichi, S Kitao, et al.
Page
of 24