Literature DB >> 7837770

Measurement of blood holoceruloplasmin by EIA using a mouse monoclonal antibody directed to holoceruloplasmin. Implication for mass screening of Wilson disease.

F Endo1, K Taketa, K Nakamura, H Awata, A Tanoue, Y Eda, I Matsuda.   

Abstract

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Year:  1994        PMID： 7837770     DOI： 10.1007/bf00711601

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  11 in total

1.  Preparation of an apoprotein from ceruloplasmin by reversible dissociation of copper.

Authors:  A G MORELL; I H SCHEINBERG
Journal:  Science       Date:  1958-03-14       Impact factor: 47.728

2.  Mechanisms of copper incorporation during the biosynthesis of human ceruloplasmin.

Authors:  M Sato; J D Gitlin
Journal:  J Biol Chem       Date:  1991-03-15       Impact factor: 5.157

3.  Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

Authors:  F Endo; A Tanoue; A Kitano; J Arata; D M Danks; C M Lapière; Y Sei; S K Wadman; I Matsuda
Journal:  J Clin Invest       Date:  1990-01       Impact factor: 14.808

4.  Screening for inborn errors of metabolism. Report of a WHO Scientific Group.

Authors: 
Journal:  World Health Organ Tech Rep Ser       Date:  1968

5.  Measurement of human serum ceruloplasmin by its p-phenylenediamine oxidase activity.

Authors:  F W Sunderman; S Nomoto
Journal:  Clin Chem       Date:  1970-11       Impact factor: 8.327

6.  Detection of vitamin K deficiency by use of an enzyme-linked immunosorbent assay for circulating abnormal prothrombin.

Authors:  K Motohara; Y Kuroki; H Kan; F Endo; I Matsuda
Journal:  Pediatr Res       Date:  1985-04       Impact factor: 3.756

7.  The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.

Authors:  P C Bull; G R Thomas; J M Rommens; J R Forbes; D W Cox
Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

8.  The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene.

Authors:  R E Tanzi; K Petrukhin; I Chernov; J L Pellequer; W Wasco; B Ross; D M Romano; E Parano; L Pavone; L M Brzustowicz
Journal:  Nat Genet       Date:  1993-12       Impact factor: 38.330

9.  Ceruloplasmin in Wilson's disease.

Authors:  N A Holtzman; M A Naughton; F L Iber; B M Gaumnitz
Journal:  J Clin Invest       Date:  1967-06       Impact factor: 14.808

10.  Determination of apoceruloplasmin by radioimmunoassay in nutritional copper deficiency, Menkes' kinky hair syndrome, Wilson's disease, and umbilical cord blood.

Authors:  I Matsuda; T Pearson; N A Holtzman
Journal:  Pediatr Res       Date:  1974-10       Impact factor: 3.756
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  4 in total

1.  Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics.

Authors:  T Ohura; D Abukawa; H Shiraishi; A Yamaguchi; S Arashima; S Hiyamuta; K Tada; K Iinuma
Journal:  J Inherit Metab Dis       Date:  1999-02       Impact factor: 4.982

2.  Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson's Disease.

Authors:  Sunhee Jung; Jeffrey R Whiteaker; Lei Zhao; Han-Wook Yoo; Amanda G Paulovich; Si Houn Hahn
Journal:  J Proteome Res       Date:  2016-12-09       Impact factor: 4.466

3.  Automation of o-dianisidine assay for ceruloplasmin activity analyses: usefulness of investigation in Wilson's disease and in hepatic encephalopathy.

Authors:  Mariacristina Siotto; Patrizio Pasqualetti; Massimo Marano; Rosanna Squitti
Journal:  J Neural Transm (Vienna)       Date:  2014-03-25       Impact factor: 3.575

4.  Diagnostic Value of Ceruloplasmin in the Diagnosis of Pediatric Wilson's Disease.

Authors:  Jung Ah Kim; Hyun Jin Kim; Jin Min Cho; Seak Hee Oh; Beom Hee Lee; Gu-Hwan Kim; Jin-Ho Choi; Kyung Mo Kim; Han-Wook Yoo
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2015-09-25
  4 in total

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