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Human Mutation
|
May 20, 2003
Human Gene Mutation Database (HGMD): 2003 update
Peter D Stenson, Edward V Ball, Matthew Mort, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 24, 2001
A novel cell culture model of chondrocyte differentiation during mammalian endochondral ossification
J O Cheung, M C Hillarby, S Ayad, et al.
Neuroimage
|
March 27, 2012
Measuring and comparing brain cortical surface area and other areal quantities
Anderson M Winkler, Mert R Sabuncu, B T Thomas Yeo, et al.
International Journal of Sport Nutrition and Exercise Metabolism
|
December 15, 2012
A 6-month trial of resistance training with milk supplementation in adolescents: effects on body composition
Kate Lambourne, Richard A Washburn, Jaehoon Lee, et al.
Brain Structure & Function
|
July 23, 2015
Cerebral functional connectivity periodically (de)synchronizes with anatomical constraints
Raphaël Liégeois, Erik Ziegler, Christophe Phillips, et al.
Toxicologic Pathology
|
March 8, 2012
Evaluation of novel urinary renal biomarkers: biological variation and reference change values
Mark D Pinches, Catherine J Betts, Susan J Bickerton, et al.
Journal of Neurophysiology
|
January 11, 2021
The detailed organization of the human cerebellum estimated by intrinsic functional connectivity within the individual
Aihuiping Xue, Ru Kong, Qing Yang, et al.
Molecular Carcinogenesis
|
January 27, 2015
Cyclic nucleotide phosphodiesterase-1C (PDE1C) drives cell proliferation, migration and invasion in glioblastoma multiforme cells in vitro
Farjana B Rowther, Weinbin Wei, Timothy P Dawson, et al.
Biorxiv : the Preprint Server for Biology
|
August 26, 2024
MULTIMODAL NEURAL CORRELATES OF CHILDHOOD PSYCHOPATHOLOGY
Jessica Royer, Valeria Kebets, Camille Piguet, et al.
American Journal of Human Genetics
|
October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia
W A Sweetman, B Rash, B Sykes, et al.
Page
of 120
Search research articles
Search
Showing results (951-960 of 1,191) with videos related to
Sort By:
Page
of 120
Human Mutation
|
May 20, 2003
Human Gene Mutation Database (HGMD): 2003 update
Peter D Stenson, Edward V Ball, Matthew Mort, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 24, 2001
A novel cell culture model of chondrocyte differentiation during mammalian endochondral ossification
J O Cheung, M C Hillarby, S Ayad, et al.
Neuroimage
|
March 27, 2012
Measuring and comparing brain cortical surface area and other areal quantities
Anderson M Winkler, Mert R Sabuncu, B T Thomas Yeo, et al.
International Journal of Sport Nutrition and Exercise Metabolism
|
December 15, 2012
A 6-month trial of resistance training with milk supplementation in adolescents: effects on body composition
Kate Lambourne, Richard A Washburn, Jaehoon Lee, et al.
Brain Structure & Function
|
July 23, 2015
Cerebral functional connectivity periodically (de)synchronizes with anatomical constraints
Raphaël Liégeois, Erik Ziegler, Christophe Phillips, et al.
Toxicologic Pathology
|
March 8, 2012
Evaluation of novel urinary renal biomarkers: biological variation and reference change values
Mark D Pinches, Catherine J Betts, Susan J Bickerton, et al.
Journal of Neurophysiology
|
January 11, 2021
The detailed organization of the human cerebellum estimated by intrinsic functional connectivity within the individual
Aihuiping Xue, Ru Kong, Qing Yang, et al.
Molecular Carcinogenesis
|
January 27, 2015
Cyclic nucleotide phosphodiesterase-1C (PDE1C) drives cell proliferation, migration and invasion in glioblastoma multiforme cells in vitro
Farjana B Rowther, Weinbin Wei, Timothy P Dawson, et al.
Biorxiv : the Preprint Server for Biology
|
August 26, 2024
MULTIMODAL NEURAL CORRELATES OF CHILDHOOD PSYCHOPATHOLOGY
Jessica Royer, Valeria Kebets, Camille Piguet, et al.
American Journal of Human Genetics
|
October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasia
W A Sweetman, B Rash, B Sykes, et al.
Page
of 120