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Vidhya Jagannathan

Showing results (31-40 of 207) with videos related to

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Animal Genetics|March 27, 2023
SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosisSarah Kiener, Eloy Castilla, Vidhya Jagannathan, et al.
Animal Genetics|August 13, 2024
Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalitiesSarah Kiener, Georg Lehner, Vidhya Jagannathan, et al.
Genes|October 27, 2022
Long-Read Transcriptome of Equine Bronchoalveolar CellsSophie Elena Sage, Pamela Nicholson, Tosso Leeb, et al.
Plos One|October 17, 2022
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosisVerena K Affolter, Sarah Kiener, Vidhya Jagannathan, et al.
Genes|February 25, 2022
<i>FYCO1</i> Frameshift Deletion in Wirehaired Pointing Griffon Dogs with Juvenile CataractGabriela Rudd Garces, Matthias Christen, Robert Loechel, et al.
Animal Genetics|April 25, 2024
Heterozygous deletion of the NSDHL gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic neviSarah Kiener, Brett Wildermuth, Nadine M Meertens, et al.
Animal Genetics|November 1, 2018
A COL2A1 de novo variant in a Holstein bulldog calfIrene Monika Häfliger, Holger Behn, Markus Freick, et al.
BMC Genomics|July 2, 2016
A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattleJørgen S Agerholm, Fintan J McEvoy, Fiona Menzi, et al.
International Journal of Molecular Sciences|February 25, 2023
Dystrophin (<i>DMD</i>) Missense Variant in Cats with Becker-Type Muscular DystrophyStephanie Hilton, Matthias Christen, Thomas Bilzer, et al.
Animal Genetics|August 25, 2022
KRT5 missense variant in a Cardigan Welsh Corgi with epidermolysis bullosa simplexSarah Kiener, Elizabeth A Mauldin, Vidhya Jagannathan, et al.
Pageof 21

Showing results (31-40 of 207) with videos related to

Sort By:
Pageof 21
Animal Genetics|March 27, 2023
SDR9C7 missense variant in a Chihuahua with non-epidermolytic ichthyosisSarah Kiener, Eloy Castilla, Vidhya Jagannathan, et al.
Animal Genetics|August 13, 2024
Heterozygous DSP in-frame deletion in a poodle with syndromic ichthyosis involving additional hair and tooth abnormalitiesSarah Kiener, Georg Lehner, Vidhya Jagannathan, et al.
Genes|October 27, 2022
Long-Read Transcriptome of Equine Bronchoalveolar CellsSophie Elena Sage, Pamela Nicholson, Tosso Leeb, et al.
Plos One|October 17, 2022
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosisVerena K Affolter, Sarah Kiener, Vidhya Jagannathan, et al.
Genes|February 25, 2022
<i>FYCO1</i> Frameshift Deletion in Wirehaired Pointing Griffon Dogs with Juvenile CataractGabriela Rudd Garces, Matthias Christen, Robert Loechel, et al.
Animal Genetics|April 25, 2024
Heterozygous deletion of the NSDHL gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic neviSarah Kiener, Brett Wildermuth, Nadine M Meertens, et al.
Animal Genetics|November 1, 2018
A COL2A1 de novo variant in a Holstein bulldog calfIrene Monika Häfliger, Holger Behn, Markus Freick, et al.
BMC Genomics|July 2, 2016
A CHRNB1 frameshift mutation is associated with familial arthrogryposis multiplex congenita in Red dairy cattleJørgen S Agerholm, Fintan J McEvoy, Fiona Menzi, et al.
International Journal of Molecular Sciences|February 25, 2023
Dystrophin (<i>DMD</i>) Missense Variant in Cats with Becker-Type Muscular DystrophyStephanie Hilton, Matthias Christen, Thomas Bilzer, et al.
Animal Genetics|August 25, 2022
KRT5 missense variant in a Cardigan Welsh Corgi with epidermolysis bullosa simplexSarah Kiener, Elizabeth A Mauldin, Vidhya Jagannathan, et al.
Pageof 21