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

Sumantra Chatterjee

Showing results (11-20 of 35) with videos related to

Pageof 4
Sort By:
Transgenic Research|August 8, 2009
The role of post-transcriptional RNA processing and plasmid vector sequences on transient transgene expression in zebrafishSumantra Chatterjee, Lin Min, R Krishna Murthy Karuturi, et al.
Plos One|January 26, 2023
Cumulative temporal vegetation indices from unoccupied aerial systems allow maize (Zea mays L.) hybrid yield to be estimated across environments with fewer flightsSumantra Chatterjee, Alper Adak, Scott Wilde, et al.
Human Molecular Genetics|March 24, 2017
Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system developmentAshish Kapoor, Dallas R Auer, Dongwon Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 2019
Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung diseaseSumantra Chatterjee, Priyanka Nandakumar, Dallas R Auer, et al.
Genome Research|November 16, 2021
A multi-enhancer <i>RET</i> regulatory code is disrupted in Hirschsprung diseaseSumantra Chatterjee, Kameko M Karasaki, Lauren E Fries, et al.
Trends in Developmental Biology|August 17, 2013
Making no bones about it: Transcription factors in vertebrate skeletogenesis and diseaseSumantra Chatterjee, V Sivakamasundari, Wenqing Jean Lee, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
<i>Sod1</i> trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal <i>Ret</i> suppression and glial remodelingGabriel Grullon, Jarod Rollins, Lauren Wilkes, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Journal of Investigative Surgery : the Official Journal of the Academy of Surgical Research|September 17, 2015
Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in GastroschisisAkhmad Makhmudi, Ahmad Hamim Sadewa, Teguh Aryandono, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Synergistic effects of <i>Ret</i> coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous systemLauren E Fries, Gabriel Grullon, Hanna E Berk-Rauch, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Transgenic Research|August 8, 2009
The role of post-transcriptional RNA processing and plasmid vector sequences on transient transgene expression in zebrafishSumantra Chatterjee, Lin Min, R Krishna Murthy Karuturi, et al.
Plos One|January 26, 2023
Cumulative temporal vegetation indices from unoccupied aerial systems allow maize (Zea mays L.) hybrid yield to be estimated across environments with fewer flightsSumantra Chatterjee, Alper Adak, Scott Wilde, et al.
Human Molecular Genetics|March 24, 2017
Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system developmentAshish Kapoor, Dallas R Auer, Dongwon Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 2019
Gene- and tissue-level interactions in normal gastrointestinal development and Hirschsprung diseaseSumantra Chatterjee, Priyanka Nandakumar, Dallas R Auer, et al.
Genome Research|November 16, 2021
A multi-enhancer <i>RET</i> regulatory code is disrupted in Hirschsprung diseaseSumantra Chatterjee, Kameko M Karasaki, Lauren E Fries, et al.
Trends in Developmental Biology|August 17, 2013
Making no bones about it: Transcription factors in vertebrate skeletogenesis and diseaseSumantra Chatterjee, V Sivakamasundari, Wenqing Jean Lee, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
<i>Sod1</i> trisomy causes ENS developmental defects and susceptibility to Hirschsprung disease via neuronal <i>Ret</i> suppression and glial remodelingGabriel Grullon, Jarod Rollins, Lauren Wilkes, et al.
Medrxiv : the Preprint Server for Health Sciences|April 3, 2026
Whole Genome Sequencing Reveals a <i>RET</i> Enhancer Risk Haplotype Associated with Hirschsprung Disease in Mowat Wilson SyndromeSydney Collins, Ibrahim Bah, Ryan Pysar, et al.
Journal of Investigative Surgery : the Official Journal of the Academy of Surgical Research|September 17, 2015
Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in GastroschisisAkhmad Makhmudi, Ahmad Hamim Sadewa, Teguh Aryandono, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Synergistic effects of <i>Ret</i> coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous systemLauren E Fries, Gabriel Grullon, Hanna E Berk-Rauch, et al.
Pageof 4