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Items: 1 to 20 of 136

1.

Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.

McGregor TL, Gurnett CA, Dobbs MB, Wise CA, Morcuende JA, Morgan TM, Menon R, Muglia LJ.

BMC Med Genet. 2011 Jul 8;12:92. doi: 10.1186/1471-2350-12-92.

2.

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms.

Akagawa H, Narita A, Yamada H, Tajima A, Krischek B, Kasuya H, Hori T, Kubota M, Saeki N, Hata A, Mizutani T, Inoue I.

Hum Genet. 2007 May;121(3-4):377-87.

PMID:
17287949
3.

Reciprocal regulation of LOX and LOXL2 expression during cell adhesion and terminal differentiation in epidermal keratinocytes.

Fujimoto E, Tajima S.

J Dermatol Sci. 2009 Aug;55(2):91-8. doi: 10.1016/j.jdermsci.2009.03.010.

PMID:
19394199
4.

Structural and functional diversity of lysyl oxidase and the LOX-like proteins.

Molnar J, Fong KS, He QP, Hayashi K, Kim Y, Fong SF, Fogelgren B, Szauter KM, Mink M, Csiszar K.

Biochim Biophys Acta. 2003 Apr 11;1647(1-2):220-4. Review.

PMID:
12686136
5.

Association of LMX1A genetic polymorphisms with susceptibility to congenital scoliosis in Chinese Han population.

Wu N, Yuan S, Liu J, Chen J, Fei Q, Liu S, Su X, Wang S, Zhang J, Li S, Wang Y, Qiu G, Wu Z.

Spine (Phila Pa 1976). 2014 Oct 1;39(21):1785-91. doi: 10.1097/BRS.0000000000000536.

PMID:
25099324
6.

Purification of enzymatically active human lysyl oxidase and lysyl oxidase-like protein from Escherichia coli inclusion bodies.

Jung ST, Kim MS, Seo JY, Kim HC, Kim Y.

Protein Expr Purif. 2003 Oct;31(2):240-6.

PMID:
14550642
7.

Lysyl oxidase and the lysyl oxidase-like protein modulate odontoblastic differentiation of human dental pulp cells.

Kim EC, Lee HJ, Kim Y.

J Endod. 2012 Jun;38(6):769-73. doi: 10.1016/j.joen.2012.03.014.

PMID:
22595110
8.

A replication study for association of 53 single nucleotide polymorphisms in ScoliScore test with adolescent idiopathic scoliosis in French-Canadian population.

Tang QL, Julien C, Eveleigh R, Bourque G, Franco A, Labelle H, Grimard G, Parent S, Ouellet J, Mac-Thiong JM, Gorman KF, Moreau A.

Spine (Phila Pa 1976). 2015 Apr 15;40(8):537-43. doi: 10.1097/BRS.0000000000000807.

PMID:
25646748
9.

Abnormal deposition of collagen around hepatocytes in Wilson's disease is associated with hepatocyte specific expression of lysyl oxidase and lysyl oxidase like protein-2.

Vadasz Z, Kessler O, Akiri G, Gengrinovitch S, Kagan HM, Baruch Y, Izhak OB, Neufeld G.

J Hepatol. 2005 Sep;43(3):499-507.

PMID:
16023247
10.

Transcriptome analysis of PPARγ target genes reveals the involvement of lysyl oxidase in human placental cytotrophoblast invasion.

Segond N, Degrelle SA, Berndt S, Clouqueur E, Rouault C, Saubamea B, Dessen P, Fong KS, Csiszar K, Badet J, Evain-Brion D, Fournier T.

PLoS One. 2013 Nov 12;8(11):e79413. doi: 10.1371/journal.pone.0079413.

11.

Lysyl oxidase-like-2 (LOXL2) is a major isoform in chondrocytes and is critically required for differentiation.

Iftikhar M, Hurtado P, Bais MV, Wigner N, Stephens DN, Gerstenfeld LC, Trackman PC.

J Biol Chem. 2011 Jan 14;286(2):909-18. doi: 10.1074/jbc.M110.155622.

12.

Association of GPR126 gene polymorphism with adolescent idiopathic scoliosis in Chinese populations.

Xu JF, Yang GH, Pan XH, Zhang SJ, Zhao C, Qiu BS, Gu HF, Hong JF, Cao L, Chen Y, Xia B, Bi Q, Wang YP.

Genomics. 2015 Feb;105(2):101-7. doi: 10.1016/j.ygeno.2014.11.009.

PMID:
25479386
13.

Transforming growth factor beta 1 is a novel susceptibility gene for adolescent idiopathic scoliosis.

Ryzhkov II, Borzilov EE, Churnosov MI, Ataman AV, Dedkov AA, Polonikov AV.

Spine (Phila Pa 1976). 2013 May 20;38(12):E699-704. doi: 10.1097/BRS.0b013e31828de9e1.

PMID:
23446766
14.

Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies.

Bykhovskaya Y, Li X, Epifantseva I, Haritunians T, Siscovick D, Aldave A, Szczotka-Flynn L, Iyengar SK, Taylor KD, Rotter JI, Rabinowitz YS.

Invest Ophthalmol Vis Sci. 2012 Jun 28;53(7):4152-7. doi: 10.1167/iovs.11-9268. Review.

15.

Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis.

Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, Ohlin A, Halldin K, Grabowski P, Tenne M, Laivuori H, Dahlman I, Andersen M, Christensen SB, Karlsson MK, Jiao H, Kere J, Gerdhem P.

Spine J. 2015 Oct 1;15(10):2239-46. doi: 10.1016/j.spinee.2015.05.013.

PMID:
25987191
16.

A replication study for association of 53 single nucleotide polymorphisms in a scoliosis prognostic test with progression of adolescent idiopathic scoliosis in Japanese.

Ogura Y, Takahashi Y, Kou I, Nakajima M, Kono K, Kawakami N, Uno K, Ito M, Minami S, Yanagida H, Taneichi H, Yonezawa I, Tsuji T, Suzuki T, Sudo H, Kotani T, Watanabe K, Chiba K, Toyama Y, Matsumoto M, Ikegawa S.

Spine (Phila Pa 1976). 2013 Jul 15;38(16):1375-9. doi: 10.1097/BRS.0b013e3182947d21.

PMID:
23591653
18.

Transforming growth factor-beta induces extracellular matrix protein cross-linking lysyl oxidase (LOX) genes in human trabecular meshwork cells.

Sethi A, Mao W, Wordinger RJ, Clark AF.

Invest Ophthalmol Vis Sci. 2011 Jul 15;52(8):5240-50. doi: 10.1167/iovs.11-7287.

19.

Lysyl oxidase-like 1 gene polymorphisms in German patients with normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma.

Wolf C, Gramer E, Müller-Myhsok B, Pasutto F, Gramer G, Wissinger B, Weisschuh N.

J Glaucoma. 2010 Feb;19(2):136-41. doi: 10.1097/IJG.0b013e31819f9330.

PMID:
19373106
20.

Lysyl oxidase polymorphisms and ischemic stroke--a case control study.

Zhang HF, Zhao KJ, Xu Y, Hong B, Zhao WY, Liu JM, Huang QH.

Mol Biol Rep. 2012 Oct;39(10):9391-7. doi: 10.1007/s11033-012-1803-9.

PMID:
22722997

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