Literature DB >> 2612218

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

A Kato1, R Asakai, E W Davie, N Aoki.   

Abstract

Chromosomal localization of the gene for human coagulation factor XI (F11) was determined by in situ hybridization using a genomic DNA probe which contained exons VIII, IX, and X of the gene. The results indicate that the gene is located at 4q35.

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Year:  1989        PMID： 2612218     DOI： 10.1159/000132844

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


  9 in total

1.  Framework multipoint map of the long arm of human chromosome 4 and telomeric localization of the gene for FSHD.

Authors:  B Weiffenbach; R G Bagley; K Falls; J Dubois; C Hyser; D Storvick; P Schultz; J R Mendell; E C Milner; S J Jacobsen
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD).

Authors:  K A Mills; K H Buetow; Y Xu; T M Ritty; K D Mathews; S E Bodrug; C Wijmenga; I Balazs; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

3.  The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD).

Authors:  M Upadhyaya; P Lunt; M Sarfarazi; W Broadhead; J Farnham; P S Harper
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

4.  Linkage localization of facioscapulohumeral muscular dystrophy (FSHD) in 4q35.

Authors:  K D Mathews; K A Mills; E P Bosch; V V Ionasescu; K R Wiles; K H Buetow; J C Murray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

5.  A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Authors:  M Upadhyaya; P W Lunt; M Sarfarazi; W Broadhead; J Daniels; M Owen; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

6.  A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates.

Authors:  K H Buetow; R Shiang; P Yang; Y Nakamura; G M Lathrop; R White; J J Wasmuth; S Wood; L D Berdahl; N J Leysens
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

7.  Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.

Authors:  Seyma Colakoglu; Turan Bayhan; Betül Tavil; Ebru Yılmaz Keskin; Volkan Cakir; Fatma Gümrük; Mualla Çetin; Selin Aytaç; Ergul Berber
Journal:  Blood Transfus       Date:  2016-10-04       Impact factor: 3.443

8.  Successful hemostatic management of major surgery for cervical spondylotic myelopathy in a patient with severe factor XI deficiency.

Authors:  Yoshiyuki Ogawa; Kunio Yanagisawa; Yuri Uchiyama; Naoki Akashi; Tokue Mieda; Haku Iizuka; Madoka Inoue; Reiko Shizuka; Masami Murakami; Naomichi Matsumoto; Hiroshi Handa
Journal:  Int J Hematol       Date:  2018-04-30       Impact factor: 2.490

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

Authors:  Seung Jun Choi; Juwon Kim; Kyung-A Lee; Jong Rak Choi; Jongha Yoo
Journal:  Ann Lab Med       Date:  2014-06-19       Impact factor: 3.464
  9 in total

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