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

Vimla S Aggarwal

Showing results (1-10 of 21) with videos related to

Pageof 3
Sort By:
Developmental Disabilities Research Reviews|July 19, 2008
Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndromeVimla S Aggarwal, Bernice E Morrow
Developmental Biology|May 27, 2010
Mesodermal Tbx1 is required for patterning the proximal mandible in miceVimla S Aggarwal, Courtney Carpenter, Laina Freyer, et al.
Developmental Biology|March 11, 2008
Identification of downstream genetic pathways of Tbx1 in the second heart fieldJun Liao, Vimla S Aggarwal, Sonja Nowotschin, et al.
BMC Developmental Biology|May 30, 2009
Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesisEvan M Braunstein, Dennis C Monks, Vimla S Aggarwal, et al.
Journal of Clinical Immunology|June 17, 2014
Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiencyNiti Sardana Agarwal, Lesley Northrop, Kwame Anyane-Yeboa, et al.
The Journal of Molecular Diagnostics : JMD|December 28, 2016
Clinical Genomic Profiling of a Diverse Array of Oncology Specimens at a Large Academic Cancer Center: Identification of Targetable Variants and Experience with ReimbursementAnthony N Sireci, Vimla S Aggarwal, Andrew T Turk, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2022
Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome SequencingRahul K Sharma, Madeleine Drusin, Joseph Hostyk, et al.
Human Molecular Genetics|September 27, 2006
Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancyVimla S Aggarwal, Jun Liao, Alexei Bondarev, et al.
Human Molecular Genetics|June 11, 2004
Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosageJun Liao, Lazaros Kochilas, Sonja Nowotschin, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Developmental Disabilities Research Reviews|July 19, 2008
Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndromeVimla S Aggarwal, Bernice E Morrow
Developmental Biology|May 27, 2010
Mesodermal Tbx1 is required for patterning the proximal mandible in miceVimla S Aggarwal, Courtney Carpenter, Laina Freyer, et al.
Developmental Biology|March 11, 2008
Identification of downstream genetic pathways of Tbx1 in the second heart fieldJun Liao, Vimla S Aggarwal, Sonja Nowotschin, et al.
BMC Developmental Biology|May 30, 2009
Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesisEvan M Braunstein, Dennis C Monks, Vimla S Aggarwal, et al.
Journal of Clinical Immunology|June 17, 2014
Tetratricopeptide repeat domain 7A (TTC7A) mutation in a newborn with multiple intestinal atresia and combined immunodeficiencyNiti Sardana Agarwal, Lesley Northrop, Kwame Anyane-Yeboa, et al.
The Journal of Molecular Diagnostics : JMD|December 28, 2016
Clinical Genomic Profiling of a Diverse Array of Oncology Specimens at a Large Academic Cancer Center: Identification of Targetable Variants and Experience with ReimbursementAnthony N Sireci, Vimla S Aggarwal, Andrew T Turk, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 12, 2022
Myosin Mutations and Sudden Sensorineural Hearing Loss: Results of Whole Exome SequencingRahul K Sharma, Madeleine Drusin, Joseph Hostyk, et al.
Human Molecular Genetics|September 27, 2006
Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancyVimla S Aggarwal, Jun Liao, Alexei Bondarev, et al.
Human Molecular Genetics|June 11, 2004
Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosageJun Liao, Lazaros Kochilas, Sonja Nowotschin, et al.
Journal of Human Genetics|September 19, 2020
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophreniaAnna Alkelai, Shahar Shohat, Lior Greenbaum, et al.
Pageof 3