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P Kemp

Showing results (361-370 of 402) with videos related to

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Nature Genetics|June 20, 2017
Variants in the fetal genome near FLT1 are associated with risk of preeclampsiaRalph McGinnis, Valgerdur Steinthorsdottir, Nicholas O Williams, et al.
Cell|January 7, 2022
Limb development genes underlie variation in human fingerprint patternsJinxi Li, James D Glover, Haiguo Zhang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2015
A genome-wide approach to children's aggressive behavior: The EAGLE consortiumIrene Pappa, Beate St Pourcain, Kelly Benke, et al.
Cell|February 26, 2021
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorptionMichelle M McDonald, Weng Hua Khoo, Pei Ying Ng, et al.
Plos Genetics|May 3, 2011
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture riskEmma L Duncan, Patrick Danoy, John P Kemp, et al.
Cell|April 2, 2021
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorptionMichelle M McDonald, Weng Hua Khoo, Pei Ying Ng, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|September 25, 2016
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric CohortsChristel M Middeldorp, Anke R Hammerschlag, Klaasjan G Ouwens, et al.
Science (New York, N.Y.)|May 16, 2015
Social evolution. Genomic signatures of evolutionary transitions from solitary to group livingKaren M Kapheim, Hailin Pan, Cai Li, et al.
Plos Genetics|July 14, 2012
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture riskHou-Feng Zheng, Jon H Tobias, Emma Duncan, et al.
The Journal of Allergy and Clinical Immunology|December 10, 2013
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variantsRalf Jp van der Valk, Liesbeth Duijts, Nicolas J Timpson, et al.
Pageof 41

Showing results (361-370 of 402) with videos related to

Sort By:
Pageof 41
Nature Genetics|June 20, 2017
Variants in the fetal genome near FLT1 are associated with risk of preeclampsiaRalph McGinnis, Valgerdur Steinthorsdottir, Nicholas O Williams, et al.
Cell|January 7, 2022
Limb development genes underlie variation in human fingerprint patternsJinxi Li, James D Glover, Haiguo Zhang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 19, 2015
A genome-wide approach to children's aggressive behavior: The EAGLE consortiumIrene Pappa, Beate St Pourcain, Kelly Benke, et al.
Cell|February 26, 2021
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorptionMichelle M McDonald, Weng Hua Khoo, Pei Ying Ng, et al.
Plos Genetics|May 3, 2011
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture riskEmma L Duncan, Patrick Danoy, John P Kemp, et al.
Cell|April 2, 2021
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorptionMichelle M McDonald, Weng Hua Khoo, Pei Ying Ng, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|September 25, 2016
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric CohortsChristel M Middeldorp, Anke R Hammerschlag, Klaasjan G Ouwens, et al.
Science (New York, N.Y.)|May 16, 2015
Social evolution. Genomic signatures of evolutionary transitions from solitary to group livingKaren M Kapheim, Hailin Pan, Cai Li, et al.
Plos Genetics|July 14, 2012
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture riskHou-Feng Zheng, Jon H Tobias, Emma Duncan, et al.
The Journal of Allergy and Clinical Immunology|December 10, 2013
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variantsRalf Jp van der Valk, Liesbeth Duijts, Nicolas J Timpson, et al.
Pageof 41