Literature DB >> 7129444

Standardization of nomenclature for transcobalamin II variants.

M Fràter-Schröder, H J Porck, A W Eriksson, S P Daiger, L L Cavalli-Sforza.   

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Year:  1982        PMID： 7129444     DOI： 10.1007/bf00274211

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  10 in total

1.  International system for human gene nomenclature (1979) ISGN (1979).

Authors:  T B Shows; C A Alper; D Bootsma; M Dorf; T Douglas; T Huisman; S Kit; H P Klinger; C Kozak; P A Lalley; D Lindsley; P J McAlpine; J K McDougall; P Meera Khan; M Meisler; N E Morton; J M Opitz; C W Partridge; R Payne; T H Roderick; P Rubinstein; F H Ruddle; M Shaw; J W Spranger; K Weiss
Journal:  Cytogenet Cell Genet       Date:  1979

2.  Hereditary transcobalamin II deficiency: clinical findings in a new family.

Authors:  W H Hitzig; U Dohmann; H J Pluss; D Vischer
Journal:  J Pediatr       Date:  1974-11       Impact factor: 4.406

3.  Neonatal megaloblastic anemia due to inherited transcobalamin II deficiency in two siblings.

Authors:  N Hakami; P E Neiman; G P Canellos; J Lazerson
Journal:  N Engl J Med       Date:  1971-11-18       Impact factor: 91.245

4.  Report of Nomenclature Meeting for alpha 1-antitrypsin, INSERM, Rouen/Bois-Guillaume-1978.

Authors:  D W Cox; A M Johnson; M K Fagerhol
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Studies on transcobalamin (TC). 1. Detection of TC II isoproteins in human serum.

Authors:  M Fràter-Schröder; W H Hitzig; R Bütler
Journal:  Blood       Date:  1979-02       Impact factor: 22.113

6.  Vitamin B12--binding proteins.

Authors:  E Jacob; S J Baker; V Herbert
Journal:  Physiol Rev       Date:  1980-07       Impact factor: 37.312

7.  Studies of a patient with megaloblastic anemia and an abnormal transcobalamin II.

Authors:  P A Seligman; L L Steiner; R H Allen
Journal:  N Engl J Med       Date:  1980-11-20       Impact factor: 91.245

8.  [Transcobalamine-II-polymorphism: biochemical and clinical aspects of rare variants].

Authors:  M Fràter-Schröder; R Lüthy; F I Haurani; W H Hitzig
Journal:  Schweiz Med Wochenschr       Date:  1979-09-29

9.  Detection of genetic variation with radioactive ligands. III. genetic polymorphism of transcobalamin II in human plasma.

Authors:  S P Daiger; M L Labowe; M Parsons; L Wang; L L Cavalli-Sforza
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

10.  Inherited lack of transcobalamin II in serum and megaloblastic anaemia: a further patient.

Authors:  J F Burman; D L Mollin; N A Sourial; R A Sladden
Journal:  Br J Haematol       Date:  1979-09       Impact factor: 6.998
  10 in total
  4 in total

1.  Variant-specific differences in human unsaturated transcobalamin II.

Authors:  H J Porck; R R Frants; J Lindemans; G J Hooghwinkel; R J Planta
Journal:  Biochem Genet       Date:  1986-02       Impact factor: 1.890

2.  Distribution of genetic variants of transcobalamin II in Nigerian black populations.

Authors:  H J Porck; A F Fleming; R R Frants
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

3.  Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells.

Authors:  F Arwert; H J Porck; M Fràter-Schröder; C Brahe; A Geurts van Kessel; A Westerveld; P Meera Khan; K Zang; R R Frants; H T Kortbeek
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

Review 4.  Genetic patterns of transcobalamin II and the relationships with congenital defects.

Authors:  M Fràter-Schröder
Journal:  Mol Cell Biochem       Date:  1983       Impact factor: 3.396
  4 in total

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