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Pak C Sham

Showing results (171-180 of 235) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 31, 2008
Genome-wide haplotype association mapping in mice identifies a genetic variant in CER1 associated with BMD and fracture in southern Chinese womenPaul L F Tang, Ching-Lung Cheung, Pak C Sham, et al.
Journal of Abnormal Psychology|October 19, 2020
Cerebellar hypoactivation is associated with impaired sensory integration in schizophreniaZhi Li, Jia Huang, Karen S Y Hung, et al.
Human Molecular Genetics|November 19, 2004
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's diseaseMercè Garcia-Barcelo, Raymond W Ganster, Vincent C H Lui, et al.
European Journal of Human Genetics : EJHG|February 28, 2018
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencingClara Sm Tang, Xuehan Zhuang, Wai-Yee Lam, et al.
Journal of Neurodevelopmental Disorders|June 20, 2025
Common and rare variant analyses implicate late-infancy cerebellar development and immune genes in ADHDYuanxin Zhong, Larry W Baum, Justin D Tubbs, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 19, 2007
Neurocognitive deficits in first-episode schizophrenic patients and their first-degree relativesXiaohong Ma, Qiang Wang, Pak C Sham, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|April 13, 2018
Early onset of disc degeneration in SM/J mice is associated with changes in ion transport systems and fibrotic eventsYing Zhang, Chi Xiong, Mateusz Kudelko, et al.
Cancer Research|April 19, 2006
High-throughput loss-of-heterozygosity study of chromosome 3p in lung cancer using single-nucleotide polymorphism markersAmy L S Tai, William Mak, Phoebe K M Ng, et al.
The Lancet. Diabetes & Endocrinology|April 16, 2014
Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysisKaixin Zhou, Louise Donnelly, Jian Yang, et al.
Plos One|December 14, 2011
The KCNJ11 E23K polymorphism and progression of glycaemia in Southern Chinese: a long-term prospective studyChloe Y Y Cheung, Annette W K Tso, Bernard M Y Cheung, et al.
Pageof 24

Showing results (171-180 of 235) with videos related to

Sort By:
Pageof 24
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 31, 2008
Genome-wide haplotype association mapping in mice identifies a genetic variant in CER1 associated with BMD and fracture in southern Chinese womenPaul L F Tang, Ching-Lung Cheung, Pak C Sham, et al.
Journal of Abnormal Psychology|October 19, 2020
Cerebellar hypoactivation is associated with impaired sensory integration in schizophreniaZhi Li, Jia Huang, Karen S Y Hung, et al.
Human Molecular Genetics|November 19, 2004
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's diseaseMercè Garcia-Barcelo, Raymond W Ganster, Vincent C H Lui, et al.
European Journal of Human Genetics : EJHG|February 28, 2018
Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencingClara Sm Tang, Xuehan Zhuang, Wai-Yee Lam, et al.
Journal of Neurodevelopmental Disorders|June 20, 2025
Common and rare variant analyses implicate late-infancy cerebellar development and immune genes in ADHDYuanxin Zhong, Larry W Baum, Justin D Tubbs, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 19, 2007
Neurocognitive deficits in first-episode schizophrenic patients and their first-degree relativesXiaohong Ma, Qiang Wang, Pak C Sham, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|April 13, 2018
Early onset of disc degeneration in SM/J mice is associated with changes in ion transport systems and fibrotic eventsYing Zhang, Chi Xiong, Mateusz Kudelko, et al.
Cancer Research|April 19, 2006
High-throughput loss-of-heterozygosity study of chromosome 3p in lung cancer using single-nucleotide polymorphism markersAmy L S Tai, William Mak, Phoebe K M Ng, et al.
The Lancet. Diabetes & Endocrinology|April 16, 2014
Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysisKaixin Zhou, Louise Donnelly, Jian Yang, et al.
Plos One|December 14, 2011
The KCNJ11 E23K polymorphism and progression of glycaemia in Southern Chinese: a long-term prospective studyChloe Y Y Cheung, Annette W K Tso, Bernard M Y Cheung, et al.
Pageof 24