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David J Cutler

Showing results (71-80 of 142) with videos related to

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Stem Cells Translational Medicine|March 4, 2023
Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell TherapyMurugadas Anbazhagan, Duke Geem, Suresh Venkateswaran, et al.
Genome Research|March 3, 2004
Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arraysChristopher W Wong, Thomas J Albert, Vinsensius B Vega, et al.
American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
Nature|April 15, 2005
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease riskEileen Sproat Emison, Andrew S McCallion, Carl S Kashuk, et al.
Inflammatory Bowel Diseases|March 27, 2012
Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixtureOloruntosin Adeyanju, David T Okou, Clifton Huang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depressionRanjana Verma, David J Cutler, Peter Holmans, et al.
Human Molecular Genetics|July 3, 2003
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locusJose L Badano, Jun Chul Kim, Bethan E Hoskins, et al.
Genome Medicine|November 16, 2023
The role of admixture in the rare variant contribution to inflammatory bowel diseaseCourtney Astore, Shivam Sharma, Sini Nagpal, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Pageof 15

Showing results (71-80 of 142) with videos related to

Sort By:
Pageof 15
Stem Cells Translational Medicine|March 4, 2023
Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell TherapyMurugadas Anbazhagan, Duke Geem, Suresh Venkateswaran, et al.
Genome Research|March 3, 2004
Tracking the evolution of the SARS coronavirus using high-throughput, high-density resequencing arraysChristopher W Wong, Thomas J Albert, Vinsensius B Vega, et al.
American Journal of Human Genetics|January 9, 2008
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autismDan E Arking, David J Cutler, Camille W Brune, et al.
Nature|April 15, 2005
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease riskEileen Sproat Emison, Andrew S McCallion, Carl S Kashuk, et al.
Inflammatory Bowel Diseases|March 27, 2012
Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixtureOloruntosin Adeyanju, David T Okou, Clifton Huang, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 19, 2007
Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depressionRanjana Verma, David J Cutler, Peter Holmans, et al.
Human Molecular Genetics|July 3, 2003
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locusJose L Badano, Jun Chul Kim, Bethan E Hoskins, et al.
Genome Medicine|November 16, 2023
The role of admixture in the rare variant contribution to inflammatory bowel diseaseCourtney Astore, Shivam Sharma, Sini Nagpal, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Rare genetic variants in <i>SEC24D</i> modify orofacial cleft phenotypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Human Genetics|September 7, 2023
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypesSarah W Curtis, Jenna C Carlson, Terri H Beaty, et al.
Pageof 15