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Vidhya Jagannathan

Showing results (41-50 of 207) with videos related to

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BMC Veterinary Research|April 19, 2015
DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattleMartin Peters, Irene Reber, Vidhya Jagannathan, et al.
Genes|October 23, 2021
<i>MYO5A</i> Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1Matthias Christen, Madeleine de le Roi, Vidhya Jagannathan, et al.
Genes|September 28, 2021
A Missense Variant in <i>SLC39A4</i> in a Litter of Turkish Van Cats with Acrodermatitis EnteropathicaSarah Kiener, Robert Cikota, Monika Welle, et al.
BMC Veterinary Research|June 15, 2016
Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1Jørgen S Agerholm, Fiona Menzi, Fintan J McEvoy, et al.
Journal of Veterinary Internal Medicine|December 21, 2019
A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosisJulien Guevar, Petra Hug, Felix Giebels, et al.
Genes|February 9, 2020
The <i>LCORL</i> Locus is under Selection in Large-Sized Pakistani Goat BreedsRashid Saif, Jan Henkel, Vidhya Jagannathan, et al.
Genes|December 9, 2020
A <i>COL7A1</i> Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis BullosaTeresa Maria Garcia, Sarah Kiener, Vidhya Jagannathan, et al.
Genes|August 28, 2025
<i>RAB24</i> Missense Variant in Dogs with Cerebellar AtaxiaCleo Schwarz, Jan Wennemuth, Julien Guevar, et al.
Plos One|October 28, 2014
Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattleLeonardo Murgiano, Vidhya Jagannathan, Valerio Calderoni, et al.
Journal of Veterinary Internal Medicine|January 8, 2021
Diagnostic potential of three serum microRNAs as biomarkers for equine sarcoid disease in horses and donkeysLucia Unger, Carlos Abril, Vinzenz Gerber, et al.
Pageof 21

Showing results (41-50 of 207) with videos related to

Sort By:
Pageof 21
BMC Veterinary Research|April 19, 2015
DNA-based diagnosis of rare diseases in veterinary medicine: a 4.4 kb deletion of ITGB4 is associated with epidermolysis bullosa in Charolais cattleMartin Peters, Irene Reber, Vidhya Jagannathan, et al.
Genes|October 23, 2021
<i>MYO5A</i> Frameshift Variant in a Miniature Dachshund with Coat Color Dilution and Neurological Defects Resembling Human Griscelli Syndrome Type 1Matthias Christen, Madeleine de le Roi, Vidhya Jagannathan, et al.
Genes|September 28, 2021
A Missense Variant in <i>SLC39A4</i> in a Litter of Turkish Van Cats with Acrodermatitis EnteropathicaSarah Kiener, Robert Cikota, Monika Welle, et al.
BMC Veterinary Research|June 15, 2016
Lethal chondrodysplasia in a family of Holstein cattle is associated with a de novo splice site variant of COL2A1Jørgen S Agerholm, Fiona Menzi, Fintan J McEvoy, et al.
Journal of Veterinary Internal Medicine|December 21, 2019
A major facilitator superfamily domain 8 frameshift variant in a cat with suspected neuronal ceroid lipofuscinosisJulien Guevar, Petra Hug, Felix Giebels, et al.
Genes|February 9, 2020
The <i>LCORL</i> Locus is under Selection in Large-Sized Pakistani Goat BreedsRashid Saif, Jan Henkel, Vidhya Jagannathan, et al.
Genes|December 9, 2020
A <i>COL7A1</i> Variant in a Litter of Neonatal Basset Hounds with Dystrophic Epidermolysis BullosaTeresa Maria Garcia, Sarah Kiener, Vidhya Jagannathan, et al.
Genes|August 28, 2025
<i>RAB24</i> Missense Variant in Dogs with Cerebellar AtaxiaCleo Schwarz, Jan Wennemuth, Julien Guevar, et al.
Plos One|October 28, 2014
Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattleLeonardo Murgiano, Vidhya Jagannathan, Valerio Calderoni, et al.
Journal of Veterinary Internal Medicine|January 8, 2021
Diagnostic potential of three serum microRNAs as biomarkers for equine sarcoid disease in horses and donkeysLucia Unger, Carlos Abril, Vinzenz Gerber, et al.
Pageof 21