Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 22

PubMed (OMIM) Links for Gene (Select 2038)

1.

Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex.

Bruce LJ, Ghosh S, King MJ, Layton DM, Mawby WJ, Stewart GW, Oldenborg PA, Delaunay J, Tanner MJ.

Blood. 2002 Sep 1;100(5):1878-85.

3.

4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis.

Perrotta S, Iolascon A, Polito R, d'Urzo G, Conte ML, Miraglia del Giudice E.

Haematologica. 1999 Jul;84(7):660-2. No abstract available.

4.

The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid.

Gwynn B, Korsgren C, Cohen CM, Ciciotte SL, Peters LL.

Genomics. 1997 Jun 15;42(3):532-5.

PMID:
9205130
5.

Human erythrocyte dematin and protein 4.2 (pallidin) are ATP binding proteins.

Azim AC, Marfatia SM, Korsgren C, Dotimas E, Cohen CM, Chishti AH.

Biochemistry. 1996 Mar 5;35(9):3001-6.

PMID:
8608138
6.

A novel mutation causing an aberrant splicing in the protein 4.2 gene associated with hereditary spherocytosis (protein 4.2Notame).

Matsuda M, Hatano N, Ideguchi H, Takahira H, Fukumaki Y.

Hum Mol Genet. 1995 Jul;4(7):1187-91.

PMID:
8528207
7.

Point mutation in the band 4.2 gene associated with autosomal recessively inherited erythrocyte band 4.2 deficiency.

Iwamoto S, Kajii E, Omi T, Kamesaki T, Akifuji Y, Ikemoto S.

Eur J Haematol. 1993 May;50(5):286-91.

PMID:
8319790
9.

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemia.

Hayette S, Dhermy D, dos Santos ME, Bozon M, Drenckhahn D, Alloisio N, Texier P, Delaunay J, Morlé L.

Blood. 1995 Jan 1;85(1):250-6.

10.

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia.

Hayette S, Morle L, Bozon M, Ghanem A, Risinger M, Korsgren C, Tanner MJ, Fattoum S, Cohen CM, Delaunay J.

Br J Haematol. 1995 Apr;89(4):762-70.

PMID:
7772513
11.

Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis.

Hayashi S, Koomoto R, Yano A, Ishigami S, Tsujino G.

Biochem Biophys Res Commun. 1974 Apr 23;57(4):1038-44. No abstract available.

PMID:
4830746
12.
14.

Hereditary disorders of the red cell membrane skeleton.

Davies KA, Lux SE.

Trends Genet. 1989 Jul;5(7):222-7. Review.

PMID:
2675425
15.

A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings.

Ghanem A, Pothier B, Marechal J, Ducluzeau MT, Morle L, Alloisio N, Feo C, Ben Abdeladhim A, Fattoum S, Delaunay J.

Br J Haematol. 1990 Jul;75(3):414-20.

PMID:
2386772
16.

Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2.

Korsgren C, Lawler J, Lambert S, Speicher D, Cohen CM.

Proc Natl Acad Sci U S A. 1990 Jan;87(2):613-7.

17.

A genetic defect of erythrocyte band 4.2 protein associated with hereditary spherocytosis.

Ideguchi H, Nishimura J, Nawata H, Hamasaki N.

Br J Haematol. 1990 Mar;74(3):347-53.

PMID:
2139792
19.

The gene for human erythrocyte protein 4.2 maps to chromosome 15q15.

Najfeld V, Ballard SG, Menninger J, Ward DC, Bouhassira EE, Schwartz RS, Nagel RL, Rybicki AC.

Am J Hum Genet. 1992 Jan;50(1):71-5.

20.

Molecular cloning of human protein 4.2: a major component of the erythrocyte membrane.

Sung LA, Chien S, Chang LS, Lambert K, Bliss SA, Bouhassira EE, Nagel RL, Schwartz RS, Rybicki AC.

Proc Natl Acad Sci U S A. 1990 Feb;87(3):955-9.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk