Literature DB >> 5665870

Electrophoretic abnormality in triosephosphate isomerase deficiency.

J C Kaplan, L Teeple, N Shore, E Beutler.   

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Year:  1968        PMID： 5665870     DOI： 10.1016/0006-291x(68)90628-1

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


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  10 in total

Review 1.  Advances in hereditary red cell enzyme anomalies.

Authors:  A Kahn; J C Kaplan; J C Dreyfus
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Electrophoretic methods for differentiating glycolytic enzymes of mouse and human origin.

Authors:  G S Omenn; P T Cohen
Journal:  In Vitro       Date:  1971 Nov-Dec

3.  [Regional localization of the genes for human LDHb, TPI, ENO2, PepB, PGK, alphaGALa, HGPRT, G6PD by interspecific hybridization (author's transl)].

Authors:  D Weil; N Van-Cong; R Rebourcet; J Frézal
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

4.  A new isozyme of triose phosphate isomerase specific to hominoids.

Authors:  H Rubinson; M C Meienhofer; J C Dreyfus
Journal:  J Mol Evol       Date:  1973-11-27       Impact factor: 2.395

5.  Prevalence of partial deficiency of red cell triosephosphate isomerase in Germany--a study of 3000 people.

Authors:  S W Eber; M Dünnwald; G Heinemann; T Hofstätter; H M Weinmann; B H Belohradsky
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Hereditary triose phosphate isomerase deficiency: seven new homozygous cases.

Authors:  R Rosa; M O Prehu; M C Calvin; J Badoual; D Alix; R Girod
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Studies on human triosephosphate isomerase. 3. Characterization of the enzyme from patients with the cri du chat syndrome.

Authors:  R J Hendrickson; R M Snapka; T H Sawyer; R W Gracy
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

8.  Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.

Authors:  S W Eber; A Pekrun; A Bardosi; M Gahr; W K Krietsch; J Krüger; R Matthei; W Schröter
Journal:  Eur J Pediatr       Date:  1991-09       Impact factor: 3.183

9.  Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease: familial and biochemical studies of a case found in Spain.

Authors:  J L Vives-Corrons; H Rubinson-Skala; M Mateo; J Estella; E Feliu; J C Dreyfus
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

10.  Origin of the triosephosphate isomerase isozymes in humans: genetic evidence for the expression of a single structural locus.

Authors:  R S Decker; H W Mohrenweiser
Journal:  Am J Hum Genet       Date:  1981-09       Impact factor: 11.025
  10 in total

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