Brenig B - Search Results

1

Skin exhibits of Dark Ronald XX are homozygous wild type at the Warmblood fragile foal syndrome causative missense variant position in lysyl hydroxylase gene PLOD1.

Zhang X, Hirschfeld M, Schafberg R, Swalve H, Brenig B. Zhang X, et al. Among authors: brenig b. Anim Genet. 2020 Oct;51(5):838-840. doi: 10.1111/age.12972. Epub 2020 Jun 17. Anim Genet. 2020. PMID: 32557718 No abstract available.

2

The equine MSH-R TaqI RFLP is not informative for hair colour in Arabian horses.

Kriegesmann B, Jansen S, Bishop M, Brenig B. Kriegesmann B, et al. Among authors: brenig b. Anim Genet. 1996 Feb;27(1):64. doi: 10.1111/j.1365-2052.1996.tb01189.x. Anim Genet. 1996. PMID: 8624048 No abstract available.

3

Analysis of canine protein C gene polymorphisms.

Leeb T, Pfeiffer I, Kopp T, Deppe A, Brenig B. Leeb T, et al. Among authors: brenig b. Anim Genet. 1999 Jun;30(3):237-8. doi: 10.1046/j.1365-2052.1999.00404-17.x. Anim Genet. 1999. PMID: 10443005 No abstract available.

4

Molecular cloning, mapping, and functional analysis of the bovine sulfate transporter SLC26a2 gene.

Brenig B, Baumgartner BG, Kriegesmann B, Habermann F, Fries R, Swalve HH. Brenig B, et al. Gene. 2003 Nov 13;319:161-6. doi: 10.1016/s0378-1119(03)00806-0. Gene. 2003. PMID: 14597181

5

Identification of a mutation in the ovine uroporphyrinogen decarboxylase (UROD) gene associated with a type of porphyria.

Nezamzadeh R, Seubert A, Pohlenz J, Brenig B. Nezamzadeh R, et al. Among authors: brenig b. Anim Genet. 2005 Aug;36(4):297-302. doi: 10.1111/j.1365-2052.2005.01301.x. Anim Genet. 2005. PMID: 16026339

6

Exclusion of a T>C sequence variant in exon 7 of the canine G(alphas) gene (GNAS1) as a causal gene for liver cancer.

Dudenbostel KJ, Neumann S, Baumgartner BG, Brenig B. Dudenbostel KJ, et al. Among authors: brenig b. Anim Genet. 2009 Oct;40(5):792. doi: 10.1111/j.1365-2052.2009.01901.x. Epub 2009 Apr 24. Anim Genet. 2009. PMID: 19422361 No abstract available.

7

Molecular genetics of coat colour variations in White Galloway and White Park cattle.

Brenig B, Beck J, Floren C, Bornemann-Kolatzki K, Wiedemann I, Hennecke S, Swalve H, Schütz E. Brenig B, et al. Anim Genet. 2013 Aug;44(4):450-3. doi: 10.1111/age.12029. Epub 2013 Feb 18. Anim Genet. 2013. PMID: 23418861

8

A study based on records taken at time of hoof trimming reveals a strong association between the IQ motif-containing GTPase-activating protein 1 (IQGAP1) gene and sole hemorrhage in Holstein cattle.

Swalve HH, Floren C, Wensch-Dorendorf M, Schöpke K, Pijl R, Wimmers K, Brenig B. Swalve HH, et al. Among authors: brenig b. J Dairy Sci. 2014;97(1):507-19. doi: 10.3168/jds.2013-6997. Epub 2013 Nov 12. J Dairy Sci. 2014. PMID: 24237756 Free article.

9

Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter.

Brenig B, Steingräber L, Shan S, Xu F, Hirschfeld M, Andag R, Spengeler M, Dietschi E, Mischke R, Leeb T. Brenig B, et al. Haematologica. 2019 Nov;104(11):2307-2313. doi: 10.3324/haematol.2018.215426. Epub 2019 Mar 7. Haematologica. 2019. PMID: 30846504 Free PMC article.

10

Processed pseudogene confounding the identification of a putative lethal recessive deletion in the bovine 60S ribosomal protein L11 gene (uL5).

Zhang X, Wacker C, Schütz E, Brenig B. Zhang X, et al. Among authors: brenig b. Anim Genet. 2020 Feb;51(1):146-147. doi: 10.1111/age.12868. Epub 2019 Oct 17. Anim Genet. 2020. PMID: 31625165 No abstract available.

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