Eric D Wieben - JoVE Visualize

Showing results (11-20 of 95) with videos related to

Pageof 10

Sort By:

Mayo Clinic Proceedings|August 14, 2002

Primer on medical genomics part II: Background principles and methods in molecular geneticsAyalew Tefferi, Eric D Wieben, Gordon W Dewald, et al.

Pharmacogenetics and Genomics|March 16, 2006

Human methylenetetrahydrofolate reductase pharmacogenomics: gene resequencing and functional genomicsYvette N Martin, Oreste E Salavaggione, Bruce W Eckloff, et al.

Journal of Neurochemistry|November 10, 2005

Human phenylethanolamine N-methyltransferase pharmacogenomics: gene re-sequencing and functional genomicsYuan Ji, Oreste E Salavaggione, Liewei Wang, et al.

British Journal of Pharmacology|August 19, 2003

Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomicsAraba A Adjei, Bianca A Thomae, Janel L Prondzinski, et al.

American Journal of Medical Genetics. Part A|June 4, 2014

Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicismRadhika Dhamija, Salman Kirmani, Xiangling Wang, et al.

Investigative Ophthalmology & Visual Science|April 21, 2018

Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal DystrophyElisabetta Soragni, Lina Petrosyan, Tommy A Rinkoski, et al.

Annals of Neurology|July 16, 2008

Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patientsDuygu Selcen, Margherita Milone, Xin-Ming Shen, et al.

European Journal of Human Genetics : EJHG|December 15, 2010

Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counselingRobert R McWilliams, Eric D Wieben, Kari G Rabe, et al.

Muscle & Nerve|September 8, 2017

Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21Jennifer M Martinez-Thompson, Zhiyv Niu, Jennifer A Tracy, et al.

Plos One|November 28, 2012

A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophyEric D Wieben, Ross A Aleff, Nirubol Tosakulwong, et al.

Pageof 10

Showing results (11-20 of 95) with videos related to

Sort By:

Pageof 10

Mayo Clinic Proceedings|August 14, 2002

Primer on medical genomics part II: Background principles and methods in molecular geneticsAyalew Tefferi, Eric D Wieben, Gordon W Dewald, et al.

Pharmacogenetics and Genomics|March 16, 2006

Human methylenetetrahydrofolate reductase pharmacogenomics: gene resequencing and functional genomicsYvette N Martin, Oreste E Salavaggione, Bruce W Eckloff, et al.

Journal of Neurochemistry|November 10, 2005

Human phenylethanolamine N-methyltransferase pharmacogenomics: gene re-sequencing and functional genomicsYuan Ji, Oreste E Salavaggione, Liewei Wang, et al.

British Journal of Pharmacology|August 19, 2003

Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomicsAraba A Adjei, Bianca A Thomae, Janel L Prondzinski, et al.

American Journal of Medical Genetics. Part A|June 4, 2014

Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicismRadhika Dhamija, Salman Kirmani, Xiangling Wang, et al.

Investigative Ophthalmology & Visual Science|April 21, 2018

Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal DystrophyElisabetta Soragni, Lina Petrosyan, Tommy A Rinkoski, et al.

Annals of Neurology|July 16, 2008

Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patientsDuygu Selcen, Margherita Milone, Xin-Ming Shen, et al.

European Journal of Human Genetics : EJHG|December 15, 2010

Prevalence of CDKN2A mutations in pancreatic cancer patients: implications for genetic counselingRobert R McWilliams, Eric D Wieben, Kari G Rabe, et al.

Muscle & Nerve|September 8, 2017

Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21Jennifer M Martinez-Thompson, Zhiyv Niu, Jennifer A Tracy, et al.

Plos One|November 28, 2012

A common trinucleotide repeat expansion within the transcription factor 4 (TCF4, E2-2) gene predicts Fuchs corneal dystrophyEric D Wieben, Ross A Aleff, Nirubol Tosakulwong, et al.

Pageof 10