Literature DB >> 17935556

Inherited disorders in Danish cattle.

Jørgen S Agerholm1.   

Abstract

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Year:  2007        PMID： 17935556     DOI： 10.1111/j.1600-0463.2007.apm_v115_s122.x

Source DB:  PubMed          Journal:  APMIS Suppl        ISSN： 0903-465X


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  10 in total

1.  First confirmed case of the bovine brachyspina syndrome in Canada.

Authors:  Jørgen S Agerholm; Josepha DeLay; Bryan Hicks; Merete Fredholm
Journal:  Can Vet J       Date:  2010-12       Impact factor: 1.008

2.  Novel identification of Factor XI deficiency in Indian Sahiwal (Bos indicus) cattle.

Authors:  Krishnendu Mondal; S Chakravarti; A K Ghosh; S Kumar; B Nayak; S Nandi; U Sarkar; Rajib Deb; A De; J Biswas
Journal:  Mol Biol Rep       Date:  2016-02-18       Impact factor: 2.316

3.  Screening for bovine leukocyte adhesion deficiency, deficiency of uridine monophosphate synthase, complex vertebral malformation, bovine citrullinaemia, and factor XI deficiency in Holstein cows reared in Turkey.

Authors:  Hasan Meydan; Mehmet A Yildiz; Jørgen S Agerholm
Journal:  Acta Vet Scand       Date:  2010-10-07       Impact factor: 1.695

4.  Epidermolysis bullosa in Danish Hereford calves is caused by a deletion in LAMC2 gene.

Authors:  Leonardo Murgiano; Natalie Wiedemar; Vidhya Jagannathan; Louise K Isling; Cord Drögemüller; Jørgen S Agerholm
Journal:  BMC Vet Res       Date:  2015-02-07       Impact factor: 2.741

5.  Use of SNP genotypes to identify carriers of harmful recessive mutations in cattle populations.

Authors:  Filippo Biscarini; Hermann Schwarzenbacher; Hubert Pausch; Ezequiel L Nicolazzi; Yuri Pirola; Stefano Biffani
Journal:  BMC Genomics       Date:  2016-11-03       Impact factor: 3.969

6.  Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene.

Authors:  Bo Thomsen; Peter H Nissen; Jørgen S Agerholm; Christian Bendixen
Journal:  Neurogenetics       Date:  2009-08-28       Impact factor: 2.660

7.  Fine mapping for Weaver syndrome in Brown Swiss cattle and the identification of 41 concordant mutations across NRCAM, PNPLA8 and CTTNBP2.

Authors:  Matthew McClure; Euisoo Kim; Derek Bickhart; Daniel Null; Tabatha Cooper; John Cole; George Wiggans; Paolo Ajmone-Marsan; Licia Colli; Enrico Santus; George E Liu; Steve Schroeder; Lakshmi Matukumalli; Curt Van Tassell; Tad Sonstegard
Journal:  PLoS One       Date:  2013-03-20       Impact factor: 3.240

Review 8.  Large animal models of rare genetic disorders: sheep as phenotypically relevant models of human genetic disease.

Authors:  Ashish R Pinnapureddy; Cherie Stayner; John McEwan; Olivia Baddeley; John Forman; Michael R Eccles
Journal:  Orphanet J Rare Dis       Date:  2015-09-02       Impact factor: 4.123

9.  Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle.

Authors:  Elisabeth Kunz; Sophie Rothammer; Hubert Pausch; Hermann Schwarzenbacher; Franz R Seefried; Kaspar Matiasek; Doris Seichter; Ingolf Russ; Ruedi Fries; Ivica Medugorac
Journal:  Genet Sel Evol       Date:  2016-03-18       Impact factor: 4.297

10.  Germline mutation within COL2A1 associated with lethal chondrodysplasia in a polled Holstein family.

Authors:  Sina Reinartz; Hartmut Mohwinkel; Christian Sürie; Maren Hellige; Karsten Feige; Deborah Eikelberg; Andreas Beineke; Julia Metzger; Ottmar Distl
Journal:  BMC Genomics       Date:  2017-10-10       Impact factor: 3.969
  10 in total

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