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Items: 18

1.

Genetic disorders in beef cattle: a review.

Ciepłoch A, Rutkowska K, Oprządek J, Poławska E.

Genes Genomics. 2017;39(5):461-471. doi: 10.1007/s13258-017-0525-8. Epub 2017 Mar 3. Review.

2.

ApoE, ApoE Receptors, and the Synapse in Alzheimer's Disease.

Lane-Donovan C, Herz J.

Trends Endocrinol Metab. 2017 Apr;28(4):273-284. doi: 10.1016/j.tem.2016.12.001. Epub 2017 Jan 2. Review.

PMID:
28057414
3.

Polyhydramnios in Lrp4 knockout mice with bilateral kidney agenesis: Defects in the pathways of amniotic fluid clearance.

Tanahashi H, Tian QB, Hara Y, Sakagami H, Endo S, Suzuki T.

Sci Rep. 2016 Feb 5;6:20241. doi: 10.1038/srep20241.

4.

Lrp4 domains differentially regulate limb/brain development and synaptic plasticity.

Pohlkamp T, Durakoglugil M, Lane-Donovan C, Xian X, Johnson EB, Hammer RE, Herz J.

PLoS One. 2015 Feb 17;10(2):e0116701. doi: 10.1371/journal.pone.0116701. eCollection 2015.

5.

More than cholesterol transporters: lipoprotein receptors in CNS function and neurodegeneration.

Lane-Donovan C, Philips GT, Herz J.

Neuron. 2014 Aug 20;83(4):771-87. doi: 10.1016/j.neuron.2014.08.005. Review.

6.

LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner.

Ohkawara B, Cabrera-Serrano M, Nakata T, Milone M, Asai N, Ito K, Ito M, Masuda A, Ito Y, Engel AG, Ohno K.

Hum Mol Genet. 2014 Apr 1;23(7):1856-68. doi: 10.1093/hmg/ddt578. Epub 2013 Nov 13.

7.

APP interacts with LRP4 and agrin to coordinate the development of the neuromuscular junction in mice.

Choi HY, Liu Y, Tennert C, Sugiura Y, Karakatsani A, Kröger S, Johnson EB, Hammer RE, Lin W, Herz J.

Elife. 2013 Aug 20;2:e00220. doi: 10.7554/eLife.00220.

8.

Structural mechanisms of the agrin-LRP4-MuSK signaling pathway in neuromuscular junction differentiation.

Zong Y, Jin R.

Cell Mol Life Sci. 2013 Sep;70(17):3077-88. doi: 10.1007/s00018-012-1209-9. Epub 2012 Nov 22. Review.

9.

Agrin binds to the N-terminal region of Lrp4 protein and stimulates association between Lrp4 and the first immunoglobulin-like domain in muscle-specific kinase (MuSK).

Zhang W, Coldefy AS, Hubbard SR, Burden SJ.

J Biol Chem. 2011 Nov 25;286(47):40624-30. doi: 10.1074/jbc.M111.279307. Epub 2011 Oct 3.

10.

Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function.

Leupin O, Piters E, Halleux C, Hu S, Kramer I, Morvan F, Bouwmeester T, Schirle M, Bueno-Lozano M, Fuentes FJ, Itin PH, Boudin E, de Freitas F, Jennes K, Brannetti B, Charara N, Ebersbach H, Geisse S, Lu CX, Bauer A, Van Hul W, Kneissel M.

J Biol Chem. 2011 Jun 3;286(22):19489-500. doi: 10.1074/jbc.M110.190330. Epub 2011 Apr 6.

11.

Lipoprotein receptors--an evolutionarily ancient multifunctional receptor family.

Dieckmann M, Dietrich MF, Herz J.

Biol Chem. 2010 Nov;391(11):1341-63. doi: 10.1515/BC.2010.129. Review.

12.

Lrp4 regulates initiation of ureteric budding and is crucial for kidney formation--a mouse model for Cenani-Lenz syndrome.

Karner CM, Dietrich MF, Johnson EB, Kappesser N, Tennert C, Percin F, Wollnik B, Carroll TJ, Herz J.

PLoS One. 2010 Apr 29;5(4):e10418. doi: 10.1371/journal.pone.0010418.

13.

Ectodomains of the LDL receptor-related proteins LRP1b and LRP4 have anchorage independent functions in vivo.

Dietrich MF, van der Weyden L, Prosser HM, Bradley A, Herz J, Adams DJ.

PLoS One. 2010 Apr 7;5(4):e9960. doi: 10.1371/journal.pone.0009960.

14.

LRP4 mutations alter Wnt/beta-catenin signaling and cause limb and kidney malformations in Cenani-Lenz syndrome.

Li Y, Pawlik B, Elcioglu N, Aglan M, Kayserili H, Yigit G, Percin F, Goodman F, Nürnberg G, Cenani A, Urquhart J, Chung BD, Ismail S, Amr K, Aslanger AD, Becker C, Netzer C, Scambler P, Eyaid W, Hamamy H, Clayton-Smith J, Hennekam R, Nürnberg P, Herz J, Temtamy SA, Wollnik B.

Am J Hum Genet. 2010 May 14;86(5):696-706. doi: 10.1016/j.ajhg.2010.03.004. Epub 2010 Apr 8.

15.

Mutations in VLDLR as a cause for autosomal recessive cerebellar ataxia with mental retardation (dysequilibrium syndrome).

Boycott KM, Bonnemann C, Herz J, Neuert S, Beaulieu C, Scott JN, Venkatasubramanian A, Parboosingh JS.

J Child Neurol. 2009 Oct;24(10):1310-5. doi: 10.1177/0883073809332696. Epub 2009 Mar 30.

16.

Expanding functions of lipoprotein receptors.

Herz J, Chen Y, Masiulis I, Zhou L.

J Lipid Res. 2009 Apr;50 Suppl:S287-92. doi: 10.1194/jlr.R800077-JLR200. Epub 2008 Nov 17.

17.

A critical analysis of disease-associated DNA polymorphisms in the genes of cattle, goat, sheep, and pig.

Ibeagha-Awemu EM, Kgwatalala P, Ibeagha AE, Zhao X.

Mamm Genome. 2008 Apr;19(4):226-45. doi: 10.1007/s00335-008-9101-5. Epub 2008 Mar 19. Review.

18.

Congenital syndactyly in cattle: four novel mutations in the low density lipoprotein receptor-related protein 4 gene (LRP4).

Drögemüller C, Leeb T, Harlizius B, Tammen I, Distl O, Höltershinken M, Gentile A, Duchesne A, Eggen A.

BMC Genet. 2007 Feb 23;8:5.

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