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Vidhya Jagannathan

Showing results (161-170 of 207) with videos related to

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Genes|October 21, 2020
<i>SLC19A3</i> Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing EncephalopathyMichaela Drögemüller, Anna Letko, Kaspar Matiasek, et al.
Scientific Reports|May 6, 2024
Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9Keijiro Mizukami, Angella Dorsey-Oresto, Karthik Raj, et al.
Genes|May 28, 2022
Independent <i>COL5A1</i> Variants in Cats with Ehlers-Danlos SyndromeSarah Kiener, Neoklis Apostolopoulos, Jennifer Schissler, et al.
Genes|October 23, 2019
Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland PoniesJocelyn Tanaka, Tosso Leeb, James Rushton, et al.
Plos Genetics|March 2, 2017
A de novo variant in the ASPRV1 gene in a dog with ichthyosisAnina Bauer, Dominik P Waluk, Arnaud Galichet, et al.
American Journal of Medical Genetics. Part A|February 7, 2015
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletionElisa Tassano, Vidhya Jagannathan, Cord Drögemüller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2023
A TNR Frameshift Variant in Weimaraner Dogs with an Exercise-Induced Paroxysmal Movement DisorderMatthias Christen, Rodrigo Gutierrez-Quintana, Matthew James, et al.
G3 (Bethesda, Md.)|December 14, 2018
Complex Structural <i>PPT1</i> Variant Associated with Non-syndromic Canine Retinal DegenerationLeonardo Murgiano, Doreen Becker, Dina Torjman, et al.
Plos Genetics|May 17, 2014
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH)Michaela Drögemüller, Vidhya Jagannathan, Doreen Becker, et al.
G3 (Bethesda, Md.)|February 26, 2017
A Nonsense Variant in the <i>ST14</i> Gene in Akhal-Teke Horses with Naked Foal SyndromeAnina Bauer, Theresa Hiemesch, Vidhya Jagannathan, et al.
Pageof 21

Showing results (161-170 of 207) with videos related to

Sort By:
Pageof 21
Genes|October 21, 2020
<i>SLC19A3</i> Loss-of-Function Variant in Yorkshire Terriers with Leigh-Like Subacute Necrotizing EncephalopathyMichaela Drögemüller, Anna Letko, Kaspar Matiasek, et al.
Scientific Reports|May 6, 2024
Increased susceptibility to Mycobacterium avium complex infection in miniature Schnauzer dogs caused by a codon deletion in CARD9Keijiro Mizukami, Angella Dorsey-Oresto, Karthik Raj, et al.
Genes|May 28, 2022
Independent <i>COL5A1</i> Variants in Cats with Ehlers-Danlos SyndromeSarah Kiener, Neoklis Apostolopoulos, Jennifer Schissler, et al.
Genes|October 23, 2019
Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland PoniesJocelyn Tanaka, Tosso Leeb, James Rushton, et al.
Plos Genetics|March 2, 2017
A de novo variant in the ASPRV1 gene in a dog with ichthyosisAnina Bauer, Dominik P Waluk, Arnaud Galichet, et al.
American Journal of Medical Genetics. Part A|February 7, 2015
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletionElisa Tassano, Vidhya Jagannathan, Cord Drögemüller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 6, 2023
A TNR Frameshift Variant in Weimaraner Dogs with an Exercise-Induced Paroxysmal Movement DisorderMatthias Christen, Rodrigo Gutierrez-Quintana, Matthew James, et al.
G3 (Bethesda, Md.)|December 14, 2018
Complex Structural <i>PPT1</i> Variant Associated with Non-syndromic Canine Retinal DegenerationLeonardo Murgiano, Doreen Becker, Dina Torjman, et al.
Plos Genetics|May 17, 2014
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH)Michaela Drögemüller, Vidhya Jagannathan, Doreen Becker, et al.
G3 (Bethesda, Md.)|February 26, 2017
A Nonsense Variant in the <i>ST14</i> Gene in Akhal-Teke Horses with Naked Foal SyndromeAnina Bauer, Theresa Hiemesch, Vidhya Jagannathan, et al.
Pageof 21