Literature DB >> 2912888

Sublocalization of the human protein C gene on chromosome 2q13-q14.

P Patracchini1, V Aiello, P Palazzi, E Calzolari, F Bernardi.   

Abstract

The localization of human protein C gene on chromosome 2 was investigated by in situ hybridization using a partial cDNA for protein C. Silver-grain analysis indicates that the protein C gene is located on 2q13-q14.

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Year:  1989        PMID： 2912888     DOI： 10.1007/BF00293902

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


  9 in total

1.  Report of the committee on the genetic-constitution of chromosomes 1 and 2.

Authors:  N E Morton; G A Bruns
Journal:  Cytogenet Cell Genet       Date:  1987

2.  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

3.  Anticoagulant properties of bovine plasma protein C following activation by thrombin.

Authors:  W Kisiel; W M Canfield; L H Ericsson; E W Davie
Journal:  Biochemistry       Date:  1977-12-27       Impact factor: 3.162

4.  Evolution and organization of the human protein C gene.

Authors:  J Plutzky; J A Hoskins; G L Long; G R Crabtree
Journal:  Proc Natl Acad Sci U S A       Date:  1986-02       Impact factor: 11.205

5.  Activated protein C stimulates the fibrinolytic activity of cultured endothelial cells and decreases antiactivator activity.

Authors:  Y Sakata; S Curriden; D Lawrence; J H Griffin; D J Loskutoff
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

Review 6.  Evolution of proteolytic enzymes.

Authors:  H Neurath
Journal:  Science       Date:  1984-04-27       Impact factor: 47.728

7.  De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma.

Authors:  E Calzolari; P Palazzi; V Aiello; E Mazzeo; P Perri; A Minelli; L del Senno; P Patracchini; F Bernardi
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

8.  The nucleotide sequence of the gene for human protein C.

Authors:  D C Foster; S Yoshitake; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  1985-07       Impact factor: 11.205

9.  The structure and evolution of a 461 amino acid human protein C precursor and its messenger RNA, based upon the DNA sequence of cloned human liver cDNAs.

Authors:  R J Beckmann; R J Schmidt; R F Santerre; J Plutzky; G R Crabtree; G L Long
Journal:  Nucleic Acids Res       Date:  1985-07-25       Impact factor: 16.971
  9 in total
  9 in total

1.  Polymorphism in the protein C gene detected by denaturing gradient gel electrophoresis.

Authors:  S Gandrille; M Alach
Journal:  Nucleic Acids Res       Date:  1991-12-25       Impact factor: 16.971

Review 2.  Protein C anticoagulant and cytoprotective pathways.

Authors:  John H Griffin; Berislav V Zlokovic; Laurent O Mosnier
Journal:  Int J Hematol       Date:  2012-04-05       Impact factor: 2.490

3.  A novel polymorphism (6376 G/T) in intron 7 of the human protein C gene.

Authors:  J M Soria; M Morell; X Estivill; N Sala
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

4.  Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13.

Authors:  Wei-Ming Chen; Yu-Fen Liu; Ming-Wei Lin; I-Chun Chen; Pei-Yu Lin; Guan-Lu Lin; Yuh-Shan Jou; Yang-Te Lin; Cathy S J Fann; Jer-Yuarn Wu; Kwang-Jen Hsiao; Shih-Feng Tsai
Journal:  Am J Hum Genet       Date:  2004-06-03       Impact factor: 11.025

5.  Protein C promoter polymorphisms associate with sepsis in children with systemic meningococcemia.

Authors:  Alexander Binder; Georg Endler; Sandra Rieger; Gotho Geishofer; Bernhard Resch; Christine Mannhalter; Werner Zenz
Journal:  Hum Genet       Date:  2007-06-14       Impact factor: 4.132

6.  Symptomatic hereditary type-II protein C deficiency caused by a missense mutation in exon IX of the protein C gene (Gly381 to Ser).

Authors:  E Wittmann; J Walter; I Pabinger-Fasching; H H Watzke
Journal:  Ann Hematol       Date:  1994-05       Impact factor: 3.673

7.  Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation.

Authors:  P Patracchini; E Calzolari; V Aiello; P Palazzi; P Banin; G Marchetti; F Bernardi
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

8.  Laboratory Limitations of Excluding Hereditary Protein C Deficiency by Chromogenic Assay: Discrepancies of Phenotype and Genotype.

Authors:  Holger Seidel; Bianca Haracska; Jennifer Naumann; Philipp Westhofen; Moritz Sebastian Hass; Johannes Philipp Kruppenbacher
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

9.  Effect on Plasma Protein S Activity in Patients Receiving the Factor Xa Inhibitors.

Authors:  Takako Terakami; Satomi Nagaya; Kenshi Hayashi; Hiroshi Furusho; Noboru Fujino; Takeshi Kato; Hidesaku Asakura; Eriko Morishita
Journal:  J Atheroscler Thromb       Date:  2021-07-30       Impact factor: 4.394
  9 in total

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