PubMed for id: 2038

Year	Number of Results
1988	2
1990	2
1991	2
1992	5
1993	2
1994	2
1995	3
1996	2
1999	2
2001	1
2002	6
2003	5
2004	1
2006	1
2007	1
2008	1
2009	2
2010	1
2011	2
2014	1
2017	1
2018	1
2020	1
2021	1
2022	2
2024	0

1

EPB42-Related Hereditary Spherocytosis.

Kalfa TA, Begtrup AH. Kalfa TA, et al. 2014 Mar 13 [updated 2022 Apr 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2014 Mar 13 [updated 2022 Apr 7]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 24624460 Free Books & Documents. Review.

2

Protein 4.2: a complex linker.

Satchwell TJ, Shoemark DK, Sessions RB, Toye AM. Satchwell TJ, et al. Blood Cells Mol Dis. 2009 May-Jun;42(3):201-10. doi: 10.1016/j.bcmd.2009.01.005. Epub 2009 Mar 9. Blood Cells Mol Dis. 2009. PMID: 19269200 Review.

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. Bhattacharyya R, et al. Biochem J. 1999 Jun 1;340 ( Pt 2)(Pt 2):505-12. Biochem J. 1999. PMID: 10333496 Free PMC article.

4

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

Dotimas E, Speicher DW, GuptaRoy B, Cohen CM. Dotimas E, et al. Biochim Biophys Acta. 1993 May 14;1148(1):19-29. doi: 10.1016/0005-2736(93)90156-t. Biochim Biophys Acta. 1993. PMID: 8499466

5

Human erythrocyte membrane protein 4.2 is palmitoylated.

Das AK, Bhattacharya R, Kundu M, Chakrabarti P, Basu J. Das AK, et al. Eur J Biochem. 1994 Sep 1;224(2):575-80. doi: 10.1111/j.1432-1033.1994.00575.x. Eur J Biochem. 1994. PMID: 7925374 Free article.

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. Takaoka Y, et al. Br J Haematol. 1994 Nov;88(3):527-33. doi: 10.1111/j.1365-2141.1994.tb05069.x. Br J Haematol. 1994. 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. Hayette S, et al. Blood. 1995 Jan 1;85(1):250-6. Blood. 1995. PMID: 7803799 Free article.

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. Hayette S, et al. Br J Haematol. 1995 Apr;89(4):762-70. doi: 10.1111/j.1365-2141.1995.tb08413.x. Br J Haematol. 1995. 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. Low PS, et al. Blood. 1991 Apr 1;77(7):1581-6. Blood. 1991. PMID: 1826225 Free article.

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. Najfeld V, et al. Am J Hum Genet. 1992 Jan;50(1):71-5. Am J Hum Genet. 1992. PMID: 1729896 Free PMC article.

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