Format
Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 44

1.

Co-expression Network Analysis Identified COL8A1 Is Associated with the Progression and Prognosis in Human Colon Adenocarcinoma.

Shang J, Wang F, Chen P, Wang X, Ding F, Liu S, Zhao Q.

Dig Dis Sci. 2018 May;63(5):1219-1228. doi: 10.1007/s10620-018-4996-5. Epub 2018 Mar 1.

PMID:
29497907
2.

Type VIII collagen is elevated in diseases associated with angiogenesis and vascular remodeling.

Hansen NU, Willumsen N, Sand JM, Larsen L, Karsdal MA, Leeming DJ.

Clin Biochem. 2016 Aug;49(12):903-8. doi: 10.1016/j.clinbiochem.2016.05.023. Epub 2016 May 24.

PMID:
27234597
3.
5.

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.

Nag A, Bochukova EG, Kremeyer B, Campbell DD, Muller H, Valencia-Duarte AV, Cardona J, Rivas IC, Mesa SC, Cuartas M, Garcia J, Bedoya G, Cornejo W, Herrera LD, Romero R, Fournier E, Reus VI, Lowe TL, Farooqi IS; Tourette Syndrome Association International Consortium for Genetics, Mathews CA, McGrath LM, Yu D, Cook E, Wang K, Scharf JM, Pauls DL, Freimer NB, Plagnol V, Ruiz-Linares A.

PLoS One. 2013;8(3):e59061. doi: 10.1371/journal.pone.0059061. Epub 2013 Mar 22.

6.

Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness.

Desronvil T, Logan-Wyatt D, Abdrabou W, Triana M, Jones R, Taheri S, Del Bono E, Pasquale LR, Olivier M, Haines JL, Fan BJ, Wiggs JL.

Mol Vis. 2010 Oct 29;16:2185-91.

7.

Keratoconus is not associated with mutations in COL8A1 and COL8A2.

Aldave AJ, Bourla N, Yellore VS, Rayner SA, Khan MA, Salem AK, Sonmez B.

Cornea. 2007 Sep;26(8):963-5.

PMID:
17721297
8.

No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.

Aldave AJ, Rayner SA, Salem AK, Yoo GL, Kim BT, Saeedian M, Sonmez B, Yellore VS.

Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3787-90.

PMID:
16936088
9.

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.

Biswas S, Munier FL, Yardley J, Hart-Holden N, Perveen R, Cousin P, Sutphin JE, Noble B, Batterbury M, Kielty C, Hackett A, Bonshek R, Ridgway A, McLeod D, Sheffield VC, Stone EM, Schorderet DF, Black GC.

Hum Mol Genet. 2001 Oct 1;10(21):2415-23.

PMID:
11689488
11.

The alpha1(VIII) and alpha2(VIII) chains of type VIII collagen can form stable homotrimeric molecules.

Illidge C, Kielty C, Shuttleworth A.

J Biol Chem. 1998 Aug 21;273(34):22091-5.

12.

Type VIII collagen.

Shuttleworth CA.

Int J Biochem Cell Biol. 1997 Oct;29(10):1145-8. Review.

PMID:
9438378
13.

The complete primary structure of the human alpha 1 (VIII) chain and assignment of its gene (COL8A1) to chromosome 3.

Muragaki Y, Mattei MG, Yamaguchi N, Olsen BR, Ninomiya Y.

Eur J Biochem. 1991 May 8;197(3):615-22.

14.

Biomarkers for Refractory Lupus Nephritis: A Microarray Study of Kidney Tissue.

Benjachat T, Tongyoo P, Tantivitayakul P, Somparn P, Hirankarn N, Prom-On S, Pisitkun P, Leelahavanichkul A, Avihingsanon Y, Townamchai N.

Int J Mol Sci. 2015 Jun 23;16(6):14276-90. doi: 10.3390/ijms160614276.

15.

Three new genetic loci (R1210C in CFH, variants in COL8A1 and RAD51B) are independently related to progression to advanced macular degeneration.

Seddon JM, Reynolds R, Yu Y, Rosner B.

PLoS One. 2014 Jan 31;9(1):e87047. doi: 10.1371/journal.pone.0087047. eCollection 2014.

16.

Crystal structure of the collagen alpha1(VIII) NC1 trimer.

Kvansakul M, Bogin O, Hohenester E, Yayon A.

Matrix Biol. 2003 Apr;22(2):145-52.

PMID:
12782141
17.

Vascular collagens: spotlight on the role of type VIII collagen in atherogenesis.

Plenz GA, Deng MC, Robenek H, Völker W.

Atherosclerosis. 2003 Jan;166(1):1-11. Review.

PMID:
12482545
18.
19.

Common variants at 1p36 are associated with superior frontal gyrus volume.

Hashimoto R, Ikeda M, Yamashita F, Ohi K, Yamamori H, Yasuda Y, Fujimoto M, Fukunaga M, Nemoto K, Takahashi T, Tochigi M, Onitsuka T, Yamasue H, Matsuo K, Iidaka T, Iwata N, Suzuki M, Takeda M, Kasai K, Ozaki N.

Transl Psychiatry. 2014 Oct 21;4:e472. doi: 10.1038/tp.2014.110.

20.

Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio study.

Beaty TH, Taub MA, Scott AF, Murray JC, Marazita ML, Schwender H, Parker MM, Hetmanski JB, Balakrishnan P, Mansilla MA, Mangold E, Ludwig KU, Noethen MM, Rubini M, Elcioglu N, Ruczinski I.

Hum Genet. 2013 Jul;132(7):771-81. doi: 10.1007/s00439-013-1283-6. Epub 2013 Mar 20.

Supplemental Content

Support Center