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Items: 1 to 20 of 39

1.

EPB42-Related Hereditary Spherocytosis.

Kalfa TA, Connor JA, Begtrup AH.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2014 Mar 13.

2.

Protein 4.2: a complex linker.

Satchwell TJ, Shoemark DK, Sessions RB, Toye AM.

Blood Cells Mol Dis. 2009 May-Jun;42(3):201-10. doi: 10.1016/j.bcmd.2009.01.005. Epub 2009 Mar 9. Review.

PMID:
19269200
3.

Mapping of a palmitoylatable band 3-binding domain of human erythrocyte membrane protein 4.2.

Bhattacharyya R, Das AK, Moitra PK, Pal B, Mandal I, Basu J.

Biochem J. 1999 Jun 1;340 ( Pt 2):505-12.

4.

Structural domain mapping and phosphorylation of human erythrocyte pallidin (band 4.2).

Dotimas E, Speicher DW, GuptaRoy B, Cohen CM.

Biochim Biophys Acta. 1993 May 14;1148(1):19-29.

PMID:
8499466
5.

Human erythrocyte membrane protein 4.2 is palmitoylated.

Das AK, Bhattacharya R, Kundu M, Chakrabarti P, Basu J.

Eur J Biochem. 1994 Sep 1;224(2):575-80.

6.

A novel mutation in the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2 Fukuoka).

Takaoka Y, Ideguchi H, Matsuda M, Sakamoto N, Takeuchi T, Fukumaki Y.

Br J Haematol. 1994 Nov;88(3):527-33.

PMID:
7819064
7.

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.

8.

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
9.

Contribution of the band 3-ankyrin interaction to erythrocyte membrane mechanical stability.

Low PS, Willardson BM, Mohandas N, Rossi M, Shohet S.

Blood. 1991 Apr 1;77(7):1581-6.

10.

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.

11.

Human erythrocyte protein 4.2, a high copy number membrane protein, is N-myristylated.

Risinger MA, Dotimas EM, Cohen CM.

J Biol Chem. 1992 Mar 15;267(8):5680-5.

12.

Human erythrocyte protein 4.2: isoform expression, differential splicing, and chromosomal assignment.

Sung LA, Chien S, Fan YS, Lin CC, Lambert K, Zhu L, Lam JS, Chang LS.

Blood. 1992 May 15;79(10):2763-70.

13.

Protein 4.2 interaction with hereditary spherocytosis mutants of the cytoplasmic domain of human anion exchanger 1.

Bustos SP, Reithmeier RA.

Biochem J. 2011 Jan 15;433(2):313-22. doi: 10.1042/BJ20101375.

PMID:
21039340
14.

Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cells.

Dahl KN, Parthasarathy R, Westhoff CM, Layton DM, Discher DE.

Blood. 2004 Feb 1;103(3):1131-6. Epub 2003 Oct 9.

15.

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.

16.

Binding of ras p21 to bands 4.2 and 6 of human erythrocyte membranes.

Tanimoto T, Hoshijima M, Kawata M, Yamamoto K, Ohmori T, Shiku H, Nakano H, Takai Y.

FEBS Lett. 1988 Jan 4;226(2):291-6.

17.

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.

19.

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.

20.

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON).

Bouhassira EE, Schwartz RS, Yawata Y, Ata K, Kanzaki A, Qiu JJ, Nagel RL, Rybicki AC.

Blood. 1992 Apr 1;79(7):1846-54.

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