About: Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I)

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scientific article published in Nature

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) scientific article published in Nature (en) im November 1974 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в Nature в листопаді 1974 (uk)
publication date	wds:Q59086900-A36D64E2-FE1C-41BF-8166-E1180810EAFA
publication date	1974-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59086900-5627C21B-25CC-466F-94C3-F72EE410E144
language of work or name	English
exact match	wds:Q59086900-7A0AEC04-F90F-466D-805C-D9A33AD663CC
exact match	https://scigraph.springernature.com/pub.10.1038/252066a0
cites work	wds:Q59086900-564A1AD1-C8F8-450D-BD17-06C9B9850924 wds:Q59086900-A65CBF51-F373-41F3-B5A0-15EC9A3D4FED wds:Q59086900-B65DFCF7-06F4-43CE-BA0A-F75E7F735CDD wds:Q59086900-E7791981-4F56-4CD4-B63D-CAF343AB5028
cites work	Subunit structure of human fibrinogen, soluble fibrin, and cross-linked insoluble fibrin γ-γ Cross-linking sites in human and bovine fibrin Cross-link in fibrin polymerized by factor 13: epsilon-(gamma-glutamyl)lysine Fibrinogen Detroit--a molecular defect in the N-terminal disulphide knot of human fibrinogen?
author name string	wds:Q59086900-91939902-0101-4319-BBDB-B69063FDE923 wds:Q59086900-9BEEF709-169F-482F-BF2B-54AC12EBD95C wds:Q59086900-C7D6F242-D8F5-40D3-A882-A39C35387666 wds:Q59086900-F1656412-6538-4391-ACB9-D66A3DD9CE96
author name string	M C Guillin A Z Budzynski D Ménaché V J Marder
rdfs:label	Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I) (en) Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (nl)
skos:prefLabel	Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I) (en) Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (nl)
name	Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I) (en) Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (nl)
title	wds:Q59086900-B497D7D3-572E-4B22-B9A6-23A34873342C
title	Defect in the gamma polypeptide chain of a congenital abnormal fibrinogen (Paris I) (en)
page(s)	wds:Q59086900-28928E83-A8EE-4E69-A8D6-386CABAB382A
page(s)	66-68
instance of	wds:Q59086900-F1A38DB2-CD4A-47A2-8CB6-1797C0589519
instance of	scholarly article
PubMed ID	wds:Q59086900-47A35E24-B607-4A25-B598-F4411F43400D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/4427684
PubMed ID	4427684
published in	wds:Q59086900-9C75947A-B27C-4FBD-B041-23D5FB3C5661
published in	Nature
issue	wds:Q59086900-3E9436E4-8314-4165-9C8E-7969A5CA38B5
volume	wds:Q59086900-289E2264-E158-4733-AFC1-11AFBCD1D1C3
issue	5478
volume	252
DOI	wds:Q59086900-2EA1B1DF-68CC-4350-AE94-97A8F5E6E5E5
DOI	http://dx.doi.org/10.1038/252066A0
DOI	10.1038/252066A0
Dimensions Publication ID	wds:Q59086900-AE14B8FC-783B-48E5-818E-A41F33144092
Dimensions Publication ID	1053044070
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59086900
is cites work of	The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2 Fibrinogen Stony Brook, a heterozygous A alpha 16Arg----Cys dysfibrinogenemia. Evaluation of diminished platelet aggregation support and of enhanced inhibition of fibrin assembly Fibrinogen Manchester. Detection of a heterozygous phenotype in the intraplatelet pool Evidence for four different polymerization sites involved in human fibrin formation Fibrinogen gamma chain locus is on chromosome 4 in man Formation and regulation of platelet and fibrin hemostatic plug A gamma methionine-310 to threonine substitution and consequent N-glycosylation at gamma asparagine-308 identified in a congenital dysfibrinogenemia associated with posttraumatic bleeding, fibrinogen Asahi Hydrolysis of fibrinogen Paris I by plasmin Studies on the structural abnormality of fibrinogen Paris I Dysfibrinogenemia. A new case: dysfibrinogenemia Giessen III (author's transl) The normal and morbid biology of fibrinogen The Genetics of Blood Coagulation
is cites work of	wds:Q67595513-2116DD00-E3F4-4BA8-9DD4-7E5B556EA535 wds:Q35199051-BCAC31EB-40ED-4021-813C-D0BC6D6FDE56 wds:Q34577564-D5BF7111-C0F8-4811-AF32-29F4659F31C2 wds:Q40608182-090556F5-3061-4DA0-B7E1-F610CA398B08 wds:Q72051510-0A144B6C-D064-4DA4-AFD2-888D94BD812E wds:Q40167399-1973B641-AA57-4558-B67D-133131BD5926 wds:Q38720376-B05588C6-35C4-4DDF-92E8-F020F36157EF wds:Q38344795-26D576E5-240B-4D1A-A331-359A08CBE362 wds:Q39787109-EFECEFB0-7245-491A-92E8-EDF4837DAE39 wds:Q36359565-78B87361-BB74-4BB8-8FF2-E216FFDF4282 wds:Q56601465-32B1F63C-9D2C-44A3-B0BB-30AF78C3BF2B wds:Q42102512-17531D63-87C9-487C-ACBA-B64A344FF586

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