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Michael Bamshad

Showing results (31-40 of 53) with videos related to

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Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Science (New York, N.Y.)|March 12, 2010
Analysis of genetic inheritance in a family quartet by whole-genome sequencingJared C Roach, Gustavo Glusman, Arian F A Smit, et al.
International Journal of Dermatology|November 19, 2015
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosisRahim Ullah, Muhammad Ansar, Zaka Ullah Durrani, et al.
American Journal of Respiratory and Critical Care Medicine|January 7, 2016
Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary DiseaseDandi Qiao, Christoph Lange, Terri H Beaty, et al.
Plos One|September 22, 2011
Host genetic risk factors for West Nile virus infection and disease progressionAbigail W Bigham, Kati J Buckingham, Sofia Husain, et al.
American Journal of Medical Genetics. Part A|March 30, 2021
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndromeClara C Hildebrandt, Nisha Patel, John M Graham, et al.
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
Human Molecular Genetics|July 29, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.
American Journal of Respiratory Cell and Molecular Biology|July 15, 2017
The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR MutationsPankaj B Agrawal, Ruobing Wang, Hongmei Lisa Li, et al.
Gastroenterology|January 11, 2015
Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstructionElena Bonora, Francesca Bianco, Lina Cordeddu, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
Scientific Reports|February 17, 2017
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosisJennifer Zieba, Wenjuan Zhang, Jessica X Chong, et al.
Science (New York, N.Y.)|March 12, 2010
Analysis of genetic inheritance in a family quartet by whole-genome sequencingJared C Roach, Gustavo Glusman, Arian F A Smit, et al.
International Journal of Dermatology|November 19, 2015
Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosisRahim Ullah, Muhammad Ansar, Zaka Ullah Durrani, et al.
American Journal of Respiratory and Critical Care Medicine|January 7, 2016
Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary DiseaseDandi Qiao, Christoph Lange, Terri H Beaty, et al.
Plos One|September 22, 2011
Host genetic risk factors for West Nile virus infection and disease progressionAbigail W Bigham, Kati J Buckingham, Sofia Husain, et al.
American Journal of Medical Genetics. Part A|March 30, 2021
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndromeClara C Hildebrandt, Nisha Patel, John M Graham, et al.
Human Molecular Genetics|February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafishRegie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
Human Molecular Genetics|July 29, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.
American Journal of Respiratory Cell and Molecular Biology|July 15, 2017
The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR MutationsPankaj B Agrawal, Ruobing Wang, Hongmei Lisa Li, et al.
Gastroenterology|January 11, 2015
Mutations in RAD21 disrupt regulation of APOB in patients with chronic intestinal pseudo-obstructionElena Bonora, Francesca Bianco, Lina Cordeddu, et al.
Pageof 6