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Tosso Leeb

Showing results (71-80 of 309) with videos related to

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The Journal of Heredity|May 24, 2007
A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogsCord Drögemüller, Ute Philipp, Bianca Haase, 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.
European Journal of Biochemistry|October 24, 2002
Cloning and characterization of the mammalian-specific nicolin 1 gene (NICN1) encoding a nuclear 24 kDa proteinBianca Backofen, Ralf Jacob, Katrin Serth, et al.
Biochimica Et Biophysica Acta|July 18, 2009
Impact of beta-galactosidase mutations on the expression of the canine lysosomal multienzyme complexRobert Kreutzer, Mihaela Kreutzer, Adrian C Sewell, et al.
Animal Genetics|March 8, 2023
Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier diseaseSarah Kiener, Ching Yang, Naomi Rich, et al.
Genes|October 27, 2022
<i>ACADM</i> Frameshift Variant in Cavalier King Charles Spaniels with Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMatthias Christen, Jos Bongers, Déborah Mathis, et al.
Genes|September 10, 2020
<i>LAMB3</i> Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis BullosaSarah Kiener, Aurore Laprais, Elizabeth A Mauldin, et al.
Animal Genetics|February 14, 2023
STK36 splice site variant in an Australian Shepherd dog with primary ciliary dyskinesiaMatthias Christen, Odette Ludwig-Peisker, Vidhya Jagannathan, et al.
Genes|December 23, 2022
<i>PCYT1A</i> Missense Variant in Vizslas with Disproportionate DwarfismOdette Ludwig-Peisker, Emily Ansel, Daniela Schweizer, et al.
Pageof 31

Showing results (71-80 of 309) with videos related to

Sort By:
Pageof 31
The Journal of Heredity|May 24, 2007
A noncoding melanophilin gene (MLPH) SNP at the splice donor of exon 1 represents a candidate causal mutation for coat color dilution in dogsCord Drögemüller, Ute Philipp, Bianca Haase, 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.
European Journal of Biochemistry|October 24, 2002
Cloning and characterization of the mammalian-specific nicolin 1 gene (NICN1) encoding a nuclear 24 kDa proteinBianca Backofen, Ralf Jacob, Katrin Serth, et al.
Biochimica Et Biophysica Acta|July 18, 2009
Impact of beta-galactosidase mutations on the expression of the canine lysosomal multienzyme complexRobert Kreutzer, Mihaela Kreutzer, Adrian C Sewell, et al.
Animal Genetics|March 8, 2023
Heterozygous ATP2A2 missense variant identified in a Shih Tzu with Darier diseaseSarah Kiener, Ching Yang, Naomi Rich, et al.
Genes|October 27, 2022
<i>ACADM</i> Frameshift Variant in Cavalier King Charles Spaniels with Medium-Chain Acyl-CoA Dehydrogenase DeficiencyMatthias Christen, Jos Bongers, Déborah Mathis, et al.
Genes|September 10, 2020
<i>LAMB3</i> Missense Variant in Australian Shepherd Dogs with Junctional Epidermolysis BullosaSarah Kiener, Aurore Laprais, Elizabeth A Mauldin, et al.
Animal Genetics|February 14, 2023
STK36 splice site variant in an Australian Shepherd dog with primary ciliary dyskinesiaMatthias Christen, Odette Ludwig-Peisker, Vidhya Jagannathan, et al.
Genes|December 23, 2022
<i>PCYT1A</i> Missense Variant in Vizslas with Disproportionate DwarfismOdette Ludwig-Peisker, Emily Ansel, Daniela Schweizer, et al.
Pageof 31