Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria X Sosa

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

Pageof 1
Sort By:
Human Mutation|September 8, 2011
Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencerQian Jiang, Tychele Turner, Maria X Sosa, et al.
Human Molecular Genetics|February 11, 2015
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphismsAshish Kapoor, Qian Jiang, Sumantra Chatterjee, et al.
Journal of Pediatric Surgery|December 6, 2014
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung diseaseGunadi, Ashish Kapoor, Albee Yun Ling, et al.
Journal of Pediatric Surgery|May 19, 2021
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjectsAshish Kapoor, Priyanka Nandakumar, Dallas R Auer, et al.
Iscience|July 21, 2019
Abnormal Behavior of Zebrafish Mutant in Dopamine Transporter Is Rescued by ClozapineGuangliang Wang, Guoqiang Zhang, Zhuyun Li, et al.
The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Cell Reports|September 12, 2019
αKlotho Regulates Age-Associated Vascular Calcification and Lifespan in ZebrafishAjeet Pratap Singh, Maria X Sosa, Jian Fang, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
Nature Genetics|September 13, 2016
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individualsGeorg B Ehret, Teresa Ferreira, Daniel I Chasman, et al.
Pageof 1

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

Sort By:
Pageof 1
Human Mutation|September 8, 2011
Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencerQian Jiang, Tychele Turner, Maria X Sosa, et al.
Human Molecular Genetics|February 11, 2015
Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphismsAshish Kapoor, Qian Jiang, Sumantra Chatterjee, et al.
Journal of Pediatric Surgery|December 6, 2014
Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung diseaseGunadi, Ashish Kapoor, Albee Yun Ling, et al.
Journal of Pediatric Surgery|May 19, 2021
Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjectsAshish Kapoor, Priyanka Nandakumar, Dallas R Auer, et al.
Iscience|July 21, 2019
Abnormal Behavior of Zebrafish Mutant in Dopamine Transporter Is Rescued by ClozapineGuangliang Wang, Guoqiang Zhang, Zhuyun Li, et al.
The New England Journal of Medicine|April 11, 2019
Molecular Genetic Anatomy and Risk Profile of Hirschsprung's DiseaseJoseph M Tilghman, Albee Y Ling, Tychele N Turner, et al.
Cell Reports|September 12, 2019
αKlotho Regulates Age-Associated Vascular Calcification and Lifespan in ZebrafishAjeet Pratap Singh, Maria X Sosa, Jian Fang, et al.
Nature|March 26, 2015
Loss of δ-catenin function in severe autismTychele N Turner, Kamal Sharma, Edwin C Oh, et al.
American Journal of Human Genetics|April 4, 2015
Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liabilityQian Jiang, Stacey Arnold, Tiffany Heanue, et al.
Nature Genetics|September 13, 2016
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individualsGeorg B Ehret, Teresa Ferreira, Daniel I Chasman, et al.
Pageof 1