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Items: 1 to 20 of 96

1.

Identification of the causative gene for Simmental arachnomelia syndrome using a network-based disease gene prioritization approach.

Jiao S, Chu Q, Wang Y, Xie Z, Hou S, Liu A, Wu H, Liu L, Geng F, Wang C, Qin C, Tan R, Huang X, Tan S, Wu M, Xu X, Liu X, Yu Y, Zhang Y.

PLoS One. 2013 May 16;8(5):e64468. doi: 10.1371/journal.pone.0064468. Print 2013.

2.
3.

[Establishment of the detection method for two causative genes of cattle arachnomelia syndrome].

Chu Q, Jiao SH, Wang YC, Liu L, Liu AR, Wu HJ, Xie ZQ, Hou SY, Geng FJ, Wang CY, Huang XX, Tan SX, Tan R, Zhang Y, Yu Y, Zhang Y.

Yi Chuan. 2013 May;35(5):623-7. Chinese.

PMID:
23732669
4.

Assignment of the locus for arachnomelia syndrome to bovine chromosome 23 in Simmental cattle.

Buitkamp J, Kühn C, Semmer J, Götz KU.

Anim Genet. 2009 Dec;40(6):894-9. doi: 10.1111/j.1365-2052.2009.01933.x. Epub 2009 Jun 5.

PMID:
19519792
5.

Syndrome of arachnomelia in Simmental cattle.

Buitkamp J, Luntz B, Emmerling R, Reichenbach HD, Weppert M, Schade B, Meier N, Götz KU.

BMC Vet Res. 2008 Oct 1;4:39. doi: 10.1186/1746-6148-4-39.

6.

SNP-based association mapping of Arachnomelia in Fleckvieh cattle.

Seichter D, Russ I, Förster M, Medugorac I.

Anim Genet. 2011 Oct;42(5):544-7. doi: 10.1111/j.1365-2052.2010.02167.x. Epub 2011 Jan 25.

PMID:
21906105
7.
8.

Screening for JH1 genetic defect carriers in Jersey cattle by a polymerase chain reaction and restriction fragment length polymorphism assay.

Zhang Y, Guo G, Huang H, Lu L, Wang L, Fang L, Liu L, Wang Y, Zhang S.

J Vet Diagn Invest. 2015 Sep;27(5):596-9. doi: 10.1177/1040638715589362. Epub 2015 Jul 15.

PMID:
26179100
9.

A miniature condition in Brahman cattle is associated with a single nucleotide mutation within the growth hormone gene.

McCormack BL, Chase CC Jr, Olson TA, Elsasser TH, Hammond AC, Welsh TH Jr, Jiang H, Randel RD, Okamura CA, Lucy MC.

Domest Anim Endocrinol. 2009 Aug;37(2):104-11. doi: 10.1016/j.domaniend.2009.04.001. Epub 2009 May 14.

PMID:
19524387
10.

A direct StyI polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) test for the myophosphorylase mutation in cattle.

Soethout EC, Verkaar EL, Jansen GH, Müller KE, Lenstra JA.

J Vet Med A Physiol Pathol Clin Med. 2002 Aug;49(6):289-90.

PMID:
12227470
11.

A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle.

Murgiano L, Jagannathan V, Piffer C, Diez-Prieto I, Bolcato M, Gentile A, Drögemüller C.

BMC Vet Res. 2016 Dec 5;12(1):276.

12.

Frequency and heritability of supernumerary teats in German simmental and German Brown Swiss cows.

Brka M, Reinsch N, Kalm E.

J Dairy Sci. 2002 Jul;85(7):1881-6.

PMID:
12201539
13.

Bovine exome sequence analysis and targeted SNP genotyping of recessive fertility defects BH1, HH2, and HH3 reveal a putative causative mutation in SMC2 for HH3.

McClure MC, Bickhart D, Null D, Vanraden P, Xu L, Wiggans G, Liu G, Schroeder S, Glasscock J, Armstrong J, Cole JB, Van Tassell CP, Sonstegard TS.

PLoS One. 2014 Mar 25;9(3):e92769. doi: 10.1371/journal.pone.0092769. eCollection 2014.

14.

Haplotype variability in the bovine MITF gene and association with piebaldism in Holstein and Simmental cattle breeds.

Fontanesi L, Scotti E, Russo V.

Anim Genet. 2012 Jun;43(3):250-6. doi: 10.1111/j.1365-2052.2011.02242.x. Epub 2011 Sep 15.

PMID:
22486495
16.

Arachnomelia in Brown Swiss cattle maps to chromosome 5.

Drögemüller C, Rossi M, Gentile A, Testoni S, Jörg H, Stranzinger G, Drögemüller M, Glowatzki-Mullis ML, Leeb T.

Mamm Genome. 2009 Jan;20(1):53-9. doi: 10.1007/s00335-008-9157-2. Epub 2008 Dec 31.

PMID:
19116736
17.

Relationships of growth hormone gene and milk protein polymorphisms to milk production traits in Simmental cattle.

Falaki M, Prandi A, Corradini C, Sneyers M, Gengler N, Massart S, Fazzini U, Burny A, Portetelle D, Renaville R.

J Dairy Res. 1997 Feb;64(1):47-56.

PMID:
9120077
18.

[Arachnomelia syndrome: a skeletal system malformation inherited disorder].

Jiao SH, Wang YC, Zhang Y.

Yi Chuan. 2011 Jan;33(1):36-9. Review. Chinese.

PMID:
21377956
19.

A 20 bp Duplication in Exon 2 of the Aristaless-Like Homeobox 4 Gene (ALX4) Is the Candidate Causative Mutation for Tibial Hemimelia Syndrome in Galloway Cattle.

Brenig B, Schütz E, Hardt M, Scheuermann P, Freick M.

PLoS One. 2015 Jun 15;10(6):e0129208. doi: 10.1371/journal.pone.0129208. eCollection 2015.

20.

Genetic description of factor XI deficiency in holstein semen in Western Japan.

Ghanem ME, Nishibori M.

Reprod Domest Anim. 2009 Oct;44(5):792-6. doi: 10.1111/j.1439-0531.2008.01080.x. Epub 2008 Sep 10.

PMID:
18992095

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