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Items: 1 to 20 of 101

1.

Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.

Kato A, Asakai R, Davie EW, Aoki N.

Cytogenet Cell Genet. 1989;52(1-2):77-8.

PMID:
2612218
2.

Dinucleotide repeat polymorphism in the human coagulation factor XI gene, intron B (F11), detected using the polymerase chain reaction.

Bodfish P, Warne D, Watkins C, Nyberg K, Spurr NK.

Nucleic Acids Res. 1991 Dec 25;19(24):6979. No abstract available.

3.

An insertion mutation of the bovine Fii gene is responsible for factor XI deficiency in Japanese black cattle.

Kunieda M, Tsuji T, Abbasi AR, Khalaj M, Ikeda M, Miyadera K, Ogawa H, Kunieda T.

Mamm Genome. 2005 May;16(5):383-9.

PMID:
16104386
4.

12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.

Youngs EL, Henkhaus RS, Hellings JA, Butler MG.

Clin Dysmorphol. 2012 Apr;21(2):93-6. doi: 10.1097/MCD.0b013e32834e9216. No abstract available.

5.

Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridization.

Avvedimento VE, Di Lauro R, Monticelli A, Bernardi F, Patracchini P, Calzolari E, Martini G, Varrone S.

Hum Genet. 1985;71(2):163-6.

PMID:
4043966
7.

Organization of the gene for human factor XI.

Asakai R, Davie EW, Chung DW.

Biochemistry. 1987 Nov 17;26(23):7221-8.

PMID:
2827746
8.

Severe factor XI deficiency in a Korean woman with a novel missense mutation (Val498Met) and duplication G mutation in exon 13 of the F11 gene.

Kwon MJ, Kim HJ, Bang SH, Kim SH.

Blood Coagul Fibrinolysis. 2008 Oct;19(7):679-83. doi: 10.1097/MBC.0b013e32830ef8f9.

PMID:
18832909
9.

RFLP for intron E of factor XI gene.

Butler MG, Parsons AD.

Nucleic Acids Res. 1990 Sep 11;18(17):5327. No abstract available.

10.

Molecular cloning of platelet factor XI, an alternative splicing product of the plasma factor XI gene.

Hsu TC, Shore SK, Seshsmma T, Bagasra O, Walsh PN.

J Biol Chem. 1998 May 29;273(22):13787-93.

11.

A novel missense mutation Asp506Gly in Exon 13 of the F11 gene in an asymptomatic Korean woman with mild factor XI deficiency.

Lee JH, Cho HS, Hyun MS, Kim HY, Kim HJ.

Korean J Lab Med. 2011 Oct;31(4):290-3. doi: 10.3343/kjlm.2011.31.4.290. Epub 2011 Oct 3.

12.

The human alpha 2(XI) collagen (COL11A2) chain. Molecular cloning of cDNA and genomic DNA reveals characteristics of a fibrillar collagen with differences in genomic organization.

Kimura T, Cheah KS, Chan SD, Lui VC, Mattei MG, van der Rest M, Ono K, Solomon E, Ninomiya Y, Olsen BR.

J Biol Chem. 1989 Aug 15;264(23):13910-6.

PMID:
2760050
13.

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

Mattei MG, Baeteman MA, Heilig R, Oberlé I, Davies K, Mandel JL, Mattei JF.

Hum Genet. 1985;69(4):327-31.

PMID:
2985491
14.

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.

Choi SJ, Kim J, Lee KA, Choi JR, Yoo J.

Ann Lab Med. 2014 Jul;34(4):332-5. doi: 10.3343/alm.2014.34.4.332. Epub 2014 Jun 19. No abstract available.

15.

Regional localization and molecular characterization of a DNA sequence on the long arm of chromosome 22.

Göttert E, Metzdorf R, Färber U, Blin N.

Hum Genet. 1989 Mar;81(4):385-7.

PMID:
2703243
16.
17.

The IL-9 receptor gene (IL9R): genomic structure, chromosomal localization in the pseudoautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter, and 18pter.

Kermouni A, Van Roost E, Arden KC, Vermeesch JR, Weiss S, Godelaine D, Flint J, Lurquin C, Szikora JP, Higgs DR, et al.

Genomics. 1995 Sep 20;29(2):371-82.

PMID:
8666384
18.

F11 rs2289252T and rs2036914C Polymorphisms Increase the Activity of Factor XI in Post-trauma Patients with Fractures Despite Thromboprophylaxis.

Song N, Tian AX, Zhang JM, Jiang HQ, Zang JC, Ma XL.

Orthop Surg. 2016 Aug;8(3):377-82. doi: 10.1111/os.12262.

PMID:
27627722
19.

Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1.

Henry I, Bernheim A, Bernard M, van der Rest M, Kimura T, Jeanpierre C, Barichard F, Berger R, Olsen BR, Ramirez F, et al.

Genomics. 1988 Jul;3(1):87-90.

PMID:
3220479
20.

The single copy gene coding for human alpha 1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13.

Boyd CD, Weliky K, Toth-Fejel S, Deak SB, Christiano AM, Mackenzie JW, Sandell LJ, Tryggvason K, Magenis E.

Hum Genet. 1986 Oct;74(2):121-5.

PMID:
3770740

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