These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 7082842)
21. The characterization of protein 4.1 Presles, a shortened variant of RBC membrane protein 4.1. Morlé L; Garbarz M; Alloisio N; Girot R; Chaveroche I; Boivin P; Delaunay J Blood; 1985 Jun; 65(6):1511-7. PubMed ID: 3995181 [TBL] [Abstract][Full Text] [Related]
22. An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells. Conboy JG; Chasis JA; Winardi R; Tchernia G; Kan YW; Mohandas N J Clin Invest; 1993 Jan; 91(1):77-82. PubMed ID: 8423235 [TBL] [Abstract][Full Text] [Related]
23. Clinical expression and laboratory detection of red blood cell membrane protein mutations. Palek J; Jarolim P Semin Hematol; 1993 Oct; 30(4):249-83. PubMed ID: 8266114 [No Abstract] [Full Text] [Related]
24. Defective spectrin dimer-dimer association in a family with transfusion dependent homozygous hereditary elliptocytosis. Evans JP; Baines AJ; Hann IM; Al-Hakim I; Knowles SM; Hoffbrand AV Br J Haematol; 1983 Jun; 54(2):163-72. PubMed ID: 6849840 [TBL] [Abstract][Full Text] [Related]
25. Homozygous hereditary elliptocytosis: implications for the function of membrane protein band 4.1. Shohet SB; Mohandas N; Tchernia G Prog Clin Biol Res; 1982; 97():45-52. PubMed ID: 7156170 [No Abstract] [Full Text] [Related]
26. Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations. Marchesi SL; Conboy J; Agre P; Letsinger JT; Marchesi VT; Speicher DW; Mohandas N J Clin Invest; 1990 Aug; 86(2):516-23. PubMed ID: 2384597 [TBL] [Abstract][Full Text] [Related]
27. Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1. Conboy JG; Shitamoto R; Parra M; Winardi R; Kabra A; Smith J; Mohandas N Blood; 1991 Nov; 78(9):2438-43. PubMed ID: 1932756 [TBL] [Abstract][Full Text] [Related]
28. Gel electrophoresis of the human erythrocyte membrane proteins: aberrant patterns in hematological and non-hematological diseases. Anselstetter V Blut; 1978 Mar; 36(3):135-44. PubMed ID: 638265 [No Abstract] [Full Text] [Related]
32. The elliptocytoses, ovalocytosis and related disorders. Nurse GT; Coetzer TL; Palek J Baillieres Clin Haematol; 1992 Jan; 5(1):187-207. PubMed ID: 1534499 [No Abstract] [Full Text] [Related]
33. Acquired elliptocytosis in chronic myeloid neoplasms: An enigmatic relationship to acquired red cell membrane protein and genetic abnormalities. Lichtman MA; Sham R Blood Cells Mol Dis; 2023 Nov; 103():102778. PubMed ID: 37379758 [TBL] [Abstract][Full Text] [Related]
34. Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells. Conboy JG Semin Hematol; 1993 Jan; 30(1):58-73. PubMed ID: 8434260 [No Abstract] [Full Text] [Related]
35. Red cell membrane alteration involving protein 4.1 and protein 3 in a case of recessively inherited haemolytic anaemia. Morlé L; Pothier B; Alloisio N; Ducluzeau MT; Marques S; Olim G; Martins e Silva J; Féo C; Garbarz M; Chaveroche I Eur J Haematol; 1987 May; 38(5):447-55. PubMed ID: 3653367 [TBL] [Abstract][Full Text] [Related]
36. Sp alpha I/65 hereditary elliptocytosis in North Africa. Alloisio N; Guetarni D; Morlé L; Pothier B; Ducluzeau MT; Soun A; Colonna P; Clerc M; Philippe N; Delaunay J Am J Hematol; 1986 Oct; 23(2):113-22. PubMed ID: 3752066 [TBL] [Abstract][Full Text] [Related]
38. [Hereditary elliptocytosis with detection of a membrane protein defect of erythrocytes]. Hochhaus A; Wutke K; Meyer M Z Gesamte Inn Med; 1988 Mar; 43(5):128-9. PubMed ID: 3388917 [TBL] [Abstract][Full Text] [Related]
39. Genetic disorders of the red cell membranes. Delaunay J FEBS Lett; 1995 Aug; 369(1):34-7. PubMed ID: 7641880 [TBL] [Abstract][Full Text] [Related]
40. Clinical disorders of the red cell membrane skeleton. Zail S Crit Rev Oncol Hematol; 1986; 5(4):397-453. PubMed ID: 2945665 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]