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Qing Kenneth Wang

Showing results (1-10 of 51) with videos related to

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The Journal of Biological Chemistry|August 4, 2009
Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35Chun Fan, Qiuyun Chen, Qing Kenneth Wang
Methods in Molecular Biology (Clifton, N.J.)|September 22, 2009
The TaqMan method for SNP genotypingGong-Qing Shen, Kalil G Abdullah, Qing Kenneth Wang
Molecular Vision|April 9, 2009
Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt diseaseQuansheng Xi, Lin Li, Elias I Traboulsi, et al.
Annals of Human Genetics|April 6, 2011
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian populationAnnabel Z Wang, Lin Li, Bin Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 12, 2009
Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese familyZhaohui Tang, Zhaoxiang Wang, Zhi Wang, et al.
Journal of Clinical Periodontology|June 26, 2009
Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosisXiaoqian Ye, Lisong Shi, Wei Yin, et al.
Journal of Human Genetics|September 26, 2009
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American familyTie Ke, Cladelis Rubio Gomez, Heidi Eliana Mateus, et al.
Journal of Lipid Research|February 5, 2008
Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MISara Bretschger Seidelmann, Lin Li, Gong-Qing Shen, et al.
Sleep Medicine|September 20, 2011
Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US populationQinbo Yang, Lin Li, Qiuyun Chen, et al.
Human Molecular Genetics|December 14, 2011
Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery diseaseStephen R Archacki, George Angheloiu, Christine S Moravec, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
The Journal of Biological Chemistry|August 4, 2009
Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35Chun Fan, Qiuyun Chen, Qing Kenneth Wang
Methods in Molecular Biology (Clifton, N.J.)|September 22, 2009
The TaqMan method for SNP genotypingGong-Qing Shen, Kalil G Abdullah, Qing Kenneth Wang
Molecular Vision|April 9, 2009
Novel ABCA4 compound heterozygous mutations cause severe progressive autosomal recessive cone-rod dystrophy presenting as Stargardt diseaseQuansheng Xi, Lin Li, Elias I Traboulsi, et al.
Annals of Human Genetics|April 6, 2011
Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian populationAnnabel Z Wang, Lin Li, Bin Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 12, 2009
Novel compound heterozygous mutations in CERKL cause autosomal recessive retinitis pigmentosa in a nonconsanguineous Chinese familyZhaohui Tang, Zhaoxiang Wang, Zhi Wang, et al.
Journal of Clinical Periodontology|June 26, 2009
Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosisXiaoqian Ye, Lisong Shi, Wei Yin, et al.
Journal of Human Genetics|September 26, 2009
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American familyTie Ke, Cladelis Rubio Gomez, Heidi Eliana Mateus, et al.
Journal of Lipid Research|February 5, 2008
Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MISara Bretschger Seidelmann, Lin Li, Gong-Qing Shen, et al.
Sleep Medicine|September 20, 2011
Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US populationQinbo Yang, Lin Li, Qiuyun Chen, et al.
Human Molecular Genetics|December 14, 2011
Comparative gene expression analysis between coronary arteries and internal mammary arteries identifies a role for the TES gene in endothelial cell functions relevant to coronary artery diseaseStephen R Archacki, George Angheloiu, Christine S Moravec, et al.
Pageof 6