About: Inherited variants of human red cell carbonic anhydrases

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scientific article published on 01 January 1980

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1980 (uk) articolo scientifico (pubblicato il 1980) (it) artículu científicu espublizáu en xineru de 1980 (ast) im Jahr 1980 veröffentlichter wissenschaftlicher Artikel (de) 1980 թվականի հունվարի 1-ին հրատարակված գիտական հոդված (hy) artikull shkencor i botuar më 01 janar 1980 (sq) scientific article published on 01 January 1980 (en)
publication date	wds:Q71523966-DF432538-63C6-467F-8853-7CFF644DB5B6
publication date	1980-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q71523966-004BEC25-5535-4759-B680-12FA50E06AAB wds:Q71523966-177BA70E-5B9A-48B1-83B6-F2785E8F04B7 wds:Q71523966-E9178EE5-5EDE-4041-B54F-D2110BAA365A
author name string	N D Carter R E Tashian A G Kendall
rdfs:label	Inherited variants of human red cell carbonic anhydrases (en) Inherited variants of human red cell carbonic anhydrases (nl)
skos:prefLabel	Inherited variants of human red cell carbonic anhydrases (en) Inherited variants of human red cell carbonic anhydrases (nl)
name	Inherited variants of human red cell carbonic anhydrases (en) Inherited variants of human red cell carbonic anhydrases (nl)
title	wds:Q71523966-D7CD5836-FB72-406F-B3C0-D0BA09AA1E1D
title	Inherited variants of human red cell carbonic anhydrases (en)
page(s)	wds:Q71523966-901971D8-1B31-417A-AF7D-A2B39ACA5FFC
page(s)	635-651
instance of	wds:Q71523966-8DFFAC22-FC3A-4FF0-8C9B-6E161351884C
instance of	scholarly article
PubMed ID	wds:Q71523966-A2778B47-59D3-40EC-9BDB-685B3157E7A0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6777336
PubMed ID	6777336
published in	wds:Q71523966-EC4206A0-104A-42E3-B194-F0320C988BC4
published in	Hemoglobin
issue	wds:Q71523966-417FCD48-7995-4323-806B-271C08C7F18F
volume	wds:Q71523966-55694BED-3C2E-4E9F-B807-AC561FA3844A
issue	5-6
volume	4
DOI	wds:Q71523966-43D9A280-F262-4B1E-9500-780683F18607
DOI	http://dx.doi.org/10.3109/03630268008997733
DOI	10.3109/03630268008997733
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71523966
is cites work of	Human hypoxanthine-guanine phosphoribosyltransferase. Demonstration of structural variants in lymphoblastoid cells derived from patients with a deficiency of the enzyme Carbonic anhydrases in normal gastrointestinal tract and gastrointestinal tumours. Separation of allelic variants by two-dimensional electrophoresis Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translation A chemical and enzymological comparison of the common major human erythrocyte carbonic anhydrase II, its minor component, and a new genetic variant, CA II Melbourne (237 Pro leads to His) Amino acid substitution and chemical characterization of a Japanese variant of carbonic anhydrase I: CA I Hiroshima-1 (86 Asp replaced by Gly) Primary distal tubular acidosis in childhood: clinical study and long-term follow-up of 28 patients Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8. Siblings with renal tubular acidosis and nerve deafness. The first family in Japan Chemical and enzymological characterization of an Indonesian variant of human erythrocyte carbonic anhydrase II, CAII Jogjakarta (17 Lys leads to Glu). A polymorphic variant of human erythrocyte carbonic anhydrase I with a widespread distribution in Australian aborigines, CAI Australia-9 (8 Asp leads to Gly): purification, properties, amino acid substitution, and possible physiological significance Cloned cDNA for rabbit erythrocyte carbonic anhydrase I: A novel erythrocyte-specific probe to study development in erythroid tissues Crystal analysis of aromatic sulfonamide binding to native and (Zn)2 adduct of human carbonic anhydrase I Michigan 1 DNA polymorphism in the 5' flanking region of the human carbonic anhydrase II gene on chromosome 8 Marked zinc activation of ester hydrolysis by a mutation, 67-His (CAT) to Arg (CGT), in the active site of human carbonic anhydrase I Biochemical genetics of macaques. III. Inheritance of carbonic anhydrase II polymorphism in rhesus monkeys
is cites work of	wds:Q36631650-BF8EB218-FB4D-4E0E-B790-23988BEB345E wds:Q40632347-67FE9EA9-A1CB-412E-AA11-CF45002B3CFD wds:Q70082966-2E3D7A18-425A-43B3-807E-DCF8B07CEBDA wds:Q28646336-FA7750D5-2570-4F0C-9384-EE2936B0E36B wds:Q37008881-EE8863A1-5BBE-4EFB-83C3-0B68F5AA5C1F wds:Q68226940-EA0EBB8A-83FD-48E4-82C9-5551CA304278 wds:Q36000418-D1064289-A41B-4AC0-BD02-B2BA7651F896 wds:Q28307596-5FE9CC2D-99BE-460F-AB41-5D653D9EE89C wds:Q37342961-123C7815-A3C8-4F8B-A370-08776B27F736 wds:Q54511637-1C697141-53AB-4525-98C0-2C45FECF79E7 wds:Q37210347-4D3DE827-2050-4DA6-9F73-BBDBFE859807 wds:Q70475325-FCB76BEE-1BE2-4514-948F-B5BA45B3CF3D wds:Q36490714-356AEE68-7100-4120-86B0-7290AE25D2A5 wds:Q57909187-E2F53698-A888-40C0-85D4-65144B22BF40 wds:Q71573437-037745FD-5E06-4C6D-AF7E-5552A183932A wds:Q71617856-BDF3CEF0-9B9A-4AAB-AD52-9C97A994200E

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