Literature DB >> 2895503

Two genes homologous with human protein S cDNA are located on chromosome 3.

J K Ploos van Amstel1, A L van der Zanden, E Bakker, P H Reitsma, R M Bertina.   

Abstract

A cDNA coding for the carboxy-terminal region of human protein S and containing a complete 3'-untranslated region, was isolated by a combination of antibody screening of a lambda gt11 human liver cDNA expression library and in situ hybridization of a pUC9 human liver cDNA library. Hybridization analysis of human total DNA with radiolabelled non-overlapping cDNA restriction fragments revealed the existence of two genes per haploid genome homologous with the protein S cDNA. Both genes were mapped to chromosome 3 using human-rodent cell hybrids. Neither of the genes showed polymorphism for sixteen different enzymes upon hybridization with the protein S cDNA.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 2895503

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  11 in total

Review 1.  The interaction between complement component C4b-binding protein and the vitamin K-dependent protein S forms a link between blood coagulation and the complement system.

Authors:  M Hessing
Journal:  Biochem J       Date:  1991-08-01       Impact factor: 3.857

2.  A CCA/CCG neutral dimorphism in the codon for Pro 626 of the human protein S gene PS alpha (PROS1).

Authors:  C M Diepstraten; J K van Amstel; P H Reitsma; R M Bertina
Journal:  Nucleic Acids Res       Date:  1991-09-25       Impact factor: 16.971

3.  The Journey of Protein S from an Anticoagulant to a Signaling Molecule.

Authors:  V S Pilli; William Plautz; Rinku Majumder
Journal:  JSM Biochem Mol Biol       Date:  2016-08-08

Review 4.  Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism.

Authors:  U Nowak-Göttl; K Auberger; U Göbel; W Kreuz; R Schneppenheim; H Vielhaber; W Zenz; B Zieger
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183

5.  Vitamin K-dependent protein S in Leydig cells of human testis.

Authors:  J Malm; X H He; A Bjartell; L Shen; P A Abrahamsson; B Dahlbäck
Journal:  Biochem J       Date:  1994-09-15       Impact factor: 3.857

6.  Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.

Authors:  Ewa Wypasek; Marek Karpinski; Martine Alhenc-Gelas; Anetta Undas
Journal:  J Genet       Date:  2017-12       Impact factor: 1.166

7.  Protein S Deficiency and Arterial Thromboembolism: A Case Report and Review of the Literature.

Authors:  Amber Fearon; Paige Pearcy; Subramanian Venkataraman; Prabodh Shah
Journal:  J Hematol (Brossard)       Date:  2019-03-30

8.  Protein S deficiency: early presentation and pulmonary hypertension.

Authors:  J O'Sullivan; R Chatuverdi; M K Bennett; S Hunter
Journal:  Arch Dis Child       Date:  1992-07       Impact factor: 3.791

9.  Three novel mutations in five unrelated subjects with hereditary protein S deficiency type I.

Authors:  P H Reitsma; H K Ploos van Amstel; R M Bertina
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

10.  Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Authors:  Maria C Pintao; A A Garcia; D Borgel; M Alhenc-Gelas; C A Spek; M C H de Visser; S Gandrille; Pieter H Reitsma
Journal:  Hum Genet       Date:  2009-05-23       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.