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Wu Lin

Showing results (641-650 of 660) with videos related to

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Blood|March 2, 2013
Higher bone marrow LGALS3 expression is an independent unfavorable prognostic factor for overall survival in patients with acute myeloid leukemiaChieh-Lung Cheng, Hsin-An Hou, Ming-Cheng Lee, et al.
Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Journal of the National Cancer Institute|June 22, 2006
A new tumor suppressor DnaJ-like heat shock protein, HLJ1, and survival of patients with non-small-cell lung carcinomaMeng-Feng Tsai, Chi-Chung Wang, Gee-Chen Chang, et al.
Neuron Glia Biology|March 17, 2007
Oligodendrocytes regulate formation of nodes of Ranvier via the recognition molecule OMgpDu-Yu Nie, Quan-Hong Ma, Janice W S Law, et al.
American Journal of Human Genetics|March 5, 2016
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar AtrophyTamar Harel, Gozde Yesil, Yavuz Bayram, et al.
Biochemical and Biophysical Research Communications|April 17, 2017
Role of GPR30 in estrogen-induced prostate epithelial apoptosis and benign prostatic hyperplasiaDeng-Liang Yang, Jia-Wen Xu, Jian-Guo Zhu, et al.
Genome Medicine|November 2, 2016
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomicsMaria Nicla Loviglio, Christine R Beck, Janson J White, et al.
BMC Medical Genomics|July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rateWu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.
American Journal of Medical Genetics. Part A|April 2, 2020
Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillationZeynep H Coban-Akdemir, Wu-Lin Charng, Mahshid Azamian, et al.
The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
Pageof 66

Showing results (641-650 of 660) with videos related to

Sort By:
Pageof 66
Blood|March 2, 2013
Higher bone marrow LGALS3 expression is an independent unfavorable prognostic factor for overall survival in patients with acute myeloid leukemiaChieh-Lung Cheng, Hsin-An Hou, Ming-Cheng Lee, et al.
Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Journal of the National Cancer Institute|June 22, 2006
A new tumor suppressor DnaJ-like heat shock protein, HLJ1, and survival of patients with non-small-cell lung carcinomaMeng-Feng Tsai, Chi-Chung Wang, Gee-Chen Chang, et al.
Neuron Glia Biology|March 17, 2007
Oligodendrocytes regulate formation of nodes of Ranvier via the recognition molecule OMgpDu-Yu Nie, Quan-Hong Ma, Janice W S Law, et al.
American Journal of Human Genetics|March 5, 2016
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar AtrophyTamar Harel, Gozde Yesil, Yavuz Bayram, et al.
Biochemical and Biophysical Research Communications|April 17, 2017
Role of GPR30 in estrogen-induced prostate epithelial apoptosis and benign prostatic hyperplasiaDeng-Liang Yang, Jia-Wen Xu, Jian-Guo Zhu, et al.
Genome Medicine|November 2, 2016
Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomicsMaria Nicla Loviglio, Christine R Beck, Janson J White, et al.
BMC Medical Genomics|July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rateWu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.
American Journal of Medical Genetics. Part A|April 2, 2020
Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillationZeynep H Coban-Akdemir, Wu-Lin Charng, Mahshid Azamian, et al.
The Journal of Clinical Investigation|January 12, 2016
Molecular etiology of arthrogryposis in multiple families of mostly Turkish originYavuz Bayram, Ender Karaca, Zeynep Coban Akdemir, et al.
Pageof 66