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Results: 1 to 20 of 102

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
[PubMed - indexed for MEDLINE]
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.

PMID:
1762944
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

Localization of the human dihydropteridine reductase gene to band p15.3 of chromosome 4 by in situ hybridization.

Brown RM, Dahl HH.

Genomics. 1987 Sep;1(1):67-70.

PMID:
3666748
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
Free Article
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

Organization of the gene for human factor XI.

Asakai R, Davie EW, Chung DW.

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

PMID:
2827746
[PubMed - indexed for MEDLINE]
10.

Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

Harper ME, Ullrich A, Saunders GF.

Proc Natl Acad Sci U S A. 1981 Jul;78(7):4458-60.

PMID:
7027261
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
9593722
[PubMed - indexed for MEDLINE]
Free Article
14.

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
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

Detection of amplified DNA sequences by reverse chromosome painting using genomic tumor DNA as probe.

Joos S, Scherthan H, Speicher MR, Schlegel J, Cremer T, Lichter P.

Hum Genet. 1993 Feb;90(6):584-9.

PMID:
8383093
[PubMed - indexed for MEDLINE]
17.

Chromosomal location and structural organization of the human deoxycytidylate deaminase gene.

Weiner KX, Ciesla J, Jaffe AB, Ketring R, Maley F, Maley GF.

J Biol Chem. 1995 Aug 11;270(32):18727-9.

PMID:
7642519
[PubMed - indexed for MEDLINE]
Free Article
18.

Assignment of the human folate transporter gene to chromosome 21q22.3 by somatic cell hybrid analysis and in situ hybridization.

Yang-Feng TL, Ma YY, Liang R, Prasad PD, Leibach FH, Ganapathy V.

Biochem Biophys Res Commun. 1995 May 25;210(3):874-9.

PMID:
7763259
[PubMed - indexed for MEDLINE]
19.

Assignment of the human collagen alpha 1 (XIII) chain gene (COL13A1) to the q22 region of chromosome 10.

Shows TB, Tikka L, Byers MG, Eddy RL, Haley LL, Henry WM, Prockop DJ, Tryggvason K.

Genomics. 1989 Jul;5(1):128-33.

PMID:
2767682
[PubMed - indexed for MEDLINE]
20.

Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes.

Johnson CV, Cool DE, Glaccum MB, Green N, Fischer EH, Bruskin A, Hill DE, Lawrence JB.

Genomics. 1993 Jun;16(3):619-29.

PMID:
8325634
[PubMed - indexed for MEDLINE]

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