Similar articles for PMID: 26763170

Year	Number of Results
1954	1
1968	1
1974	1
1976	1
1992	2
1993	2
1995	4
1996	1
1997	1
1998	1
1999	1
2002	2
2003	1
2004	4
2005	2
2006	1
2007	5
2008	1
2009	3
2010	2
2011	7
2012	6
2013	2
2014	3
2015	9
2016	18
2017	6
2018	5
2019	6
2020	9
2021	4
2022	9
2024	0

1

A transposable element insertion in APOB causes cholesterol deficiency in Holstein cattle.

Menzi F, Besuchet-Schmutz N, Fragnière M, Hofstetter S, Jagannathan V, Mock T, Raemy A, Studer E, Mehinagic K, Regenscheit N, Meylan M, Schmitz-Hsu F, Drögemüller C. Menzi F, et al. Anim Genet. 2016 Apr;47(2):253-7. doi: 10.1111/age.12410. Epub 2016 Jan 13. Anim Genet. 2016. PMID: 26763170 Free PMC article.

2

The Holstein Friesian Lethal Haplotype 5 (HH5) Results from a Complete Deletion of TBF1M and Cholesterol Deficiency (CDH) from an ERV-(LTR) Insertion into the Coding Region of APOB.

Schütz E, Wehrhahn C, Wanjek M, Bortfeld R, Wemheuer WE, Beck J, Brenig B. Schütz E, et al. PLoS One. 2016 Apr 29;11(4):e0154602. doi: 10.1371/journal.pone.0154602. eCollection 2016. PLoS One. 2016. PMID: 27128314 Free PMC article.

3

Clinicopathological Phenotype of Autosomal Recessive Cholesterol Deficiency in Holstein Cattle.

Mock T, Mehinagic K, Menzi F, Studer E, Oevermann A, Stoffel MH, Drögemüller C, Meylan M, Regenscheit N. Mock T, et al. J Vet Intern Med. 2016 Jul;30(4):1369-75. doi: 10.1111/jvim.13976. Epub 2016 Jun 8. J Vet Intern Med. 2016. PMID: 27279263 Free PMC article.

4

Rapid Communication: Cholesterol deficiency-associated APOB mutation impacts lipid metabolism in Holstein calves and breeding bulls.

Gross JJ, Schwinn AC, Schmitz-Hsu F, Menzi F, Drögemüller C, Albrecht C, Bruckmaier RM. Gross JJ, et al. J Anim Sci. 2016 Apr;94(4):1761-6. doi: 10.2527/jas.2016-0439. J Anim Sci. 2016. PMID: 27136033

5

APOB-associated cholesterol deficiency in Holstein cattle is not a simple recessive disease.

Häfliger IM, Hofstetter S, Mock T, Stettler MH, Meylan M, Mehinagic K, Stokar-Regenscheit N, Drögemüller C. Häfliger IM, et al. Anim Genet. 2019 Aug;50(4):372-375. doi: 10.1111/age.12801. Epub 2019 Jun 18. Anim Genet. 2019. PMID: 31215050 Free PMC article.

6

Identification of a haplotype associated with cholesterol deficiency and increased juvenile mortality in Holstein cattle.

Kipp S, Segelke D, Schierenbeck S, Reinhardt F, Reents R, Wurmser C, Pausch H, Fries R, Thaller G, Tetens J, Pott J, Haas D, Raddatz BB, Hewicker-Trautwein M, Proios I, Schmicke M, Grünberg W. Kipp S, et al. J Dairy Sci. 2016 Nov;99(11):8915-8931. doi: 10.3168/jds.2016-11118. Epub 2016 Sep 7. J Dairy Sci. 2016. PMID: 27614835 Free article.

7

Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia.

Di Costanzo A, Di Leo E, Noto D, Cefalù AB, Minicocci I, Polito L, D'Erasmo L, Cantisani V, Spina R, Tarugi P, Averna M, Arca M. Di Costanzo A, et al. J Clin Lipidol. 2017 Sep-Oct;11(5):1234-1242. doi: 10.1016/j.jacl.2017.06.013. Epub 2017 Jun 24. J Clin Lipidol. 2017. PMID: 28733173

8

Allele-biased expression of the bovine APOB gene associated with the cholesterol deficiency defect suggests cis-regulatory enhancer effects of the LTR retrotransposon insertion.

Becker D, Weikard R, Heimes A, Hadlich F, Hammon HM, Meyerholz MM, Petzl W, Zerbe H, Schuberth HJ, Hoedemaker M, Schmicke M, Engelmann S, Kühn C. Becker D, et al. Sci Rep. 2022 Aug 5;12(1):13469. doi: 10.1038/s41598-022-17798-5. Sci Rep. 2022. PMID: 35931741 Free PMC article.

9

Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia.

Whitfield AJ, Marais AD, Robertson K, Barrett PH, van Bockxmeer FM, Burnett JR. Whitfield AJ, et al. Hum Mutat. 2003 Aug;22(2):178. doi: 10.1002/humu.9163. Hum Mutat. 2003. PMID: 12872264

10

Identification of the bovine Arachnomelia mutation by massively parallel sequencing implicates sulfite oxidase (SUOX) in bone development.

Drögemüller C, Tetens J, Sigurdsson S, Gentile A, Testoni S, Lindblad-Toh K, Leeb T. Drögemüller C, et al. PLoS Genet. 2010 Aug 26;6(8):e1001079. doi: 10.1371/journal.pgen.1001079. PLoS Genet. 2010. PMID: 20865119 Free PMC article.

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