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The Journal of Biological Chemistry
|
December 15, 1993
Cloning and expression of a cDNA for the human prostaglandin E receptor EP1 subtype
C D Funk, L Furci, G A FitzGerald, et al.
Molecular Biology of the Cell
|
February 22, 2013
ZYX-1, the unique zyxin protein of Caenorhabditis elegans, is involved in dystrophin-dependent muscle degeneration
Claire Lecroisey, Nicolas Brouilly, Hiroshi Qadota, et al.
Journal of Inherited Metabolic Disease
|
December 31, 1998
Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?
L Thuillier, B Chadefaux-Vekemans, J P Bonnefont, et al.
The Journal of Biological Chemistry
|
June 20, 1998
The putative cofactor TIF1alpha is a protein kinase that is hyperphosphorylated upon interaction with liganded nuclear receptors
R A Fraser, D J Heard, S Adam, et al.
American Journal of Human Genetics
|
June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number
P E McAndrew, D W Parsons, L R Simard, et al.
Oncology
|
September 1, 1993
A new device for the treatment of pleural malignancies: intrapleural chemohyperthermia preliminary report
P Y Carry, A Brachet, F N Gilly, et al.
Journal of Endocrinological Investigation
|
September 10, 2014
Combined pituitary hormone deficiency: current and future status
F Castinetti, R Reynaud, M-H Quentien, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 6, 1999
New class of biphenylene dibenzazocinones as potent ligands for the human EP1 prostanoid receptor
R Ruel, P Lacombe, M Abramovitz, et al.
The Journal of Biological Chemistry
|
August 12, 1994
Immunological identification and functional quantitation of retinoic acid and retinoid X receptor proteins in human skin
G J Fisher, H S Talwar, J H Xiao, et al.
Nature Genetics
|
January 1, 1995
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients
T G Thompson, C J DiDonato, L R Simard, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 128) with videos related to
Sort By:
Page
of 13
The Journal of Biological Chemistry
|
December 15, 1993
Cloning and expression of a cDNA for the human prostaglandin E receptor EP1 subtype
C D Funk, L Furci, G A FitzGerald, et al.
Molecular Biology of the Cell
|
February 22, 2013
ZYX-1, the unique zyxin protein of Caenorhabditis elegans, is involved in dystrophin-dependent muscle degeneration
Claire Lecroisey, Nicolas Brouilly, Hiroshi Qadota, et al.
Journal of Inherited Metabolic Disease
|
December 31, 1998
Does the polymorphism 677C-T of the 5,10-methylenetetrahydrofolate reductase gene contribute to homocysteine-related vascular disease?
L Thuillier, B Chadefaux-Vekemans, J P Bonnefont, et al.
The Journal of Biological Chemistry
|
June 20, 1998
The putative cofactor TIF1alpha is a protein kinase that is hyperphosphorylated upon interaction with liganded nuclear receptors
R A Fraser, D J Heard, S Adam, et al.
American Journal of Human Genetics
|
June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy number
P E McAndrew, D W Parsons, L R Simard, et al.
Oncology
|
September 1, 1993
A new device for the treatment of pleural malignancies: intrapleural chemohyperthermia preliminary report
P Y Carry, A Brachet, F N Gilly, et al.
Journal of Endocrinological Investigation
|
September 10, 2014
Combined pituitary hormone deficiency: current and future status
F Castinetti, R Reynaud, M-H Quentien, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 6, 1999
New class of biphenylene dibenzazocinones as potent ligands for the human EP1 prostanoid receptor
R Ruel, P Lacombe, M Abramovitz, et al.
The Journal of Biological Chemistry
|
August 12, 1994
Immunological identification and functional quantitation of retinoic acid and retinoid X receptor proteins in human skin
G J Fisher, H S Talwar, J H Xiao, et al.
Nature Genetics
|
January 1, 1995
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patients
T G Thompson, C J DiDonato, L R Simard, et al.
Page
of 13