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Biochemistry
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April 10, 2002
Sterol efflux to apolipoprotein A-I originates from caveolin-rich microdomains and potentiates PDGF-dependent protein kinase activity
P E Fielding, J S Russel, T A Spencer, et al.
Biochemistry
|
May 15, 2023
The Y46D Mutation Destabilizes Dense Packing of the Second Greek Key Pair of Human γC-Crystallin Causing Congenital Nuclear Cataracts
Venkata Pulla Rao Vendra, Christian Ostrowski, Rebecca Clark, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical
|
May 1, 2018
Multiple sclerosis: Executive dysfunction, task switching and the role of attention
M Clough, P Foletta, A N Frohman, et al.
Clinical and Diagnostic Virology
|
February 1, 1997
The reliability of saliva as a sample for the detection of hepatitis A immunoglobulins under various sampling conditions
B J O'Farrell, E Rajan, S S Albloushi, et al.
Journal of Human Genetics
|
July 13, 2006
Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1
Xiangming Guo, Huangxuan Shen, Xueshan Xiao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 11, 1999
Determinants of peak bone mass: clinical and genetic analyses in a young female Canadian cohort
L A Rubin, G A Hawker, V D Peltekova, et al.
The Journal of Biological Chemistry
|
August 15, 1992
Site-directed mutagenesis and structure-function analysis of the human apolipoprotein A-I. Relation between lecithin-cholesterol acyltransferase activation and lipid binding
A Minnich, X Collet, A Roghani, et al.
Genes
|
September 28, 2024
Phenotypic and Genotypic Features of a Chinese Cohort with Retinal Hemangioblastoma
Liqin Gao, Feng Zhang, J Fielding Hejtmancik, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 14, 2012
Genotype-phenotype correlations in Bardet-Biedl syndrome
Anthony B Daniels, Michael A Sandberg, Jianjun Chen, et al.
Human Genetics
|
June 8, 2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3
Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, et al.
Page
of 50
Search research articles
Search
Showing results (301-310 of 493) with videos related to
Sort By:
Page
of 50
Biochemistry
|
April 10, 2002
Sterol efflux to apolipoprotein A-I originates from caveolin-rich microdomains and potentiates PDGF-dependent protein kinase activity
P E Fielding, J S Russel, T A Spencer, et al.
Biochemistry
|
May 15, 2023
The Y46D Mutation Destabilizes Dense Packing of the Second Greek Key Pair of Human γC-Crystallin Causing Congenital Nuclear Cataracts
Venkata Pulla Rao Vendra, Christian Ostrowski, Rebecca Clark, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical
|
May 1, 2018
Multiple sclerosis: Executive dysfunction, task switching and the role of attention
M Clough, P Foletta, A N Frohman, et al.
Clinical and Diagnostic Virology
|
February 1, 1997
The reliability of saliva as a sample for the detection of hepatitis A immunoglobulins under various sampling conditions
B J O'Farrell, E Rajan, S S Albloushi, et al.
Journal of Human Genetics
|
July 13, 2006
Cataracts, ataxia, short stature, and mental retardation in a Chinese family mapped to Xpter-q13.1
Xiangming Guo, Huangxuan Shen, Xueshan Xiao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 11, 1999
Determinants of peak bone mass: clinical and genetic analyses in a young female Canadian cohort
L A Rubin, G A Hawker, V D Peltekova, et al.
The Journal of Biological Chemistry
|
August 15, 1992
Site-directed mutagenesis and structure-function analysis of the human apolipoprotein A-I. Relation between lecithin-cholesterol acyltransferase activation and lipid binding
A Minnich, X Collet, A Roghani, et al.
Genes
|
September 28, 2024
Phenotypic and Genotypic Features of a Chinese Cohort with Retinal Hemangioblastoma
Liqin Gao, Feng Zhang, J Fielding Hejtmancik, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
March 14, 2012
Genotype-phenotype correlations in Bardet-Biedl syndrome
Anthony B Daniels, Michael A Sandberg, Jianjun Chen, et al.
Human Genetics
|
June 8, 2019
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3
Xueshan Xiao, Wenmin Sun, Jiamin Ouyang, et al.
Page
of 50