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Literature DB >> 6714981

Regional mapping of clotting factors VII and X to 13q34. Expression of factor VII through chromosome 8.

J de Grouchy, M D Dautzenberg, C Turleau, S Beguin, F Chavin-Colin.

Abstract

Blood clotting factors were investigated in a patient with trisomy 8 mosaicism, a patient with an r(13), and a patient with distal trisomy 13q. Results are compatible with the assignment of the structural genes of factors VII and X to 13q34 and the existence of a regulatory mechanism associated with chromosome 8 controlling the expression of factor VII alone.

Entities: Gene Species

Mesh：

Substances：
Factor VII
Factor X

Year: 1984 PMID： 6714981 DOI： 10.1007/bf00286607

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

12 in total

1. Coagulation studies in patients with trisomy 8 syndrome.

Authors: S Stenbjerg; S Husted; A Bernsen; P Jacobsen; J Nielsen; K Rasmussen
Journal: Ann Genet Date: 1975-12

2. [Monosomy 7qter (author's transl)].

Authors: C Turleau; J de Grouchy; F Perignon; G Lenoir
Journal: Ann Genet Date: 1979

3. [Coagulation factor VII deficiency in 3 patients with trisomy 8].

Authors: J de Grouchy; F Josso; S Beguin; C Turleau; P Jalbert; C Laurent
Journal: Ann Genet Date: 1974-06

4. Factor VII antibody-neutralizing material in hereditary and acquired factor VII deficiency.

Authors: S H Goodnight; D I Feinstein; B Osterud; S I Rapaport
Journal: Blood Date: 1971-07 Impact factor: 22.113

5. [Trisomy 13qter by tandem duplication 46, XX, dir dup 13 (q21 qter), 9qh+].

Authors: J de Grouchy; C Turleau; F Danis; G Kohout; M L Briard
Journal: Ann Genet Date: 1978-12

6. Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7.

Authors: B Biederman; P Bowen
Journal: Hum Genet Date: 1978-02-23 Impact factor: 4.132

7. Partial 4q duplication due to inherited der(13),t(4;13)(q26;q34)mat in a girl with a deficiency of factor X.

Authors: C Stoll; M P Roth
Journal: Hum Genet Date: 1980 Impact factor: 4.132

8. Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band.

Authors: J de Grouchy; C Turleau
Journal: Humangenetik Date: 1974

9. Trisomy 8 mosaicism syndrome.

Authors: R M Fineman; R C Ablow; R O Howard; J Albright; W R Breg
Journal: Pediatrics Date: 1975-11 Impact factor: 7.124

10. Complete and partial trisomy of different segments of chromosome 8: case reports and review.

Authors: R M Fineman; R C Ablow; W R Breg; S D Wing; J S Rose; S L Rothman; J Warpinski
Journal: Clin Genet Date: 1979-12 Impact factor: 4.438

11 in total

Review 1. Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

Authors: M J Pettenati; N Rao; C Johnson; R Hayworth; K Crandall; O Huff; I T Thomas
Journal: Hum Genet Date: 1992-08 Impact factor: 4.132

2. Association of protein Z and factor VII gene polymorphisms with risk of cerebral hemorrhage: a case-control and a family-based association study in a Chinese Han population.

Authors: Yi Zeng; Le Zhang; Zhiping Hu; Qidong Yang; Mingming Ma; Baoqiong Liu; Jian Xia; Hongwei Xu; Yunhai Liu; Xiaoping Du
Journal: J Genet Date: 2016-06 Impact factor: 1.166

3. The coagulation factor VII regulator is located on 8p23.1.

Authors: K Fagan; I Wilkinson; M Allen; S Brownlea
Journal: Hum Genet Date: 1988-08 Impact factor: 4.132

4. Mapping through somatic cell hybrids and cDNA probes of protein C to chromosome 2, factor X to chromosome 13, and alpha 1-acid glycoprotein to chromosome 9.

Authors: M Rocchi; L Roncuzzi; R Santamaria; N Archidiacono; L Dente; G Romeo
Journal: Hum Genet Date: 1986-09 Impact factor: 4.132