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kw.\*:("Protéine 4.2")

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Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cellsDAHL, Kris Noel; PARTHASARATHY, Ranganath; WESTHOFF, Connie M et al.Blood. 2004, Vol 103, Num 3, pp 1131-1136, issn 0006-4971, 6 p.Article

Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2)VAN DEN AKKER, Emile; SATCHWELL, Timothy J; PELLEGRIN, Stephanie et al.Haematologica (Roma). 2010, Vol 95, Num 8, pp 1278-1286, issn 0390-6078, 9 p.Article

Protein-4.2 association with band 3 (AE1, SLCA4) in Xenopus oocytes : effects of three natural protein-4.2 mutations associated with hemolytic anemiaTOYE, Ashley M; GHOSH, Sandip; YOUNG, Mark T et al.Blood. 2005, Vol 105, Num 10, pp 4088-4095, issn 0006-4971, 8 p.Article

Increased rotational mobility and extractability of band 3 from protein 4.2-deficient erythrocyte membranes : Evidence of a role for protein 4.2 in strengthening the band 3-cytoskeleton linkageRYBICKI, A. C; SCHWARTZ, R. S; HUSTEDT, E. J et al.Blood. 1996, Vol 88, Num 7, pp 2745-2753, issn 0006-4971Article

Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complexBRUCE, Lesley J; GHOSH, Sandip; KING, May Jean et al.Blood. 2002, Vol 100, Num 5, pp 1878-1885, issn 0006-4971, 8 p.Article

Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47MOURO-CHANTELOUP, Isabelle; DELAUNAY, Jean; GANE, Pierre et al.Blood. 2003, Vol 101, Num 1, pp 338-344, issn 0006-4971, 7 p.Article

Molecular cloning of human protein 4.2: a major component of the erythrocyte membraneLANPING AMY SUNG; SHU CHIEN; LONG-SHENG CHANG et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 3, pp 955-959, issn 0027-8424, 5 p.Article

The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallidGWYNN, B; KORSGREN, C; COHEN, C. M et al.Genomics (San Diego, Calif.). 1997, Vol 42, Num 3, pp 532-535, issn 0888-7543Article

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemiaHAYETTE, S; MORLE, L; BOZON, M et al.British journal of haematology. 1995, Vol 89, Num 4, pp 762-770, issn 0007-1048Article

Structural domain mapping and phosphorylation of human erythrocyte pallidin (band 4.2)DOTIMAS, E; SPEICHER, D. W; BIPASHA GUPTAROY et al.Biochimica et biophysica acta. Biomembranes. 1993, Vol 1148, Num 1, pp 19-29, issn 0005-2736Article

An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form on hereditary hemolytic anemia protein 4.2NIPPONBOUHASSIRA, E. E; SCHWARTZ, R. S; YAWATA, Y et al.Blood. 1992, Vol 79, Num 7, pp 1846-1854, issn 0006-4971Article

Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosisKANZAKI, A; HAYETTE, S; YAWATA, Y et al.British journal of haematology. 1997, Vol 99, Num 3, pp 522-530, issn 0007-1048Article

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 et al.Human molecular genetics (Print). 1995, Vol 4, Num 7, pp 1187-1191, issn 0964-6906Article

A deletional frameshift mutation in protein 4.2 gene (allele 4.2 Lisboa) associated with hereditary hemolytic anemiaHAYETTE, S; DHERMY, D; DOS SANTOS, M.-E et al.Blood. 1995, Vol 85, Num 1, pp 250-256, issn 0006-4971Article

Band 3 anion exchanger and its involvement in erythrocyte and kidney disordersTANNER, Michael J. A.Current opinion in hematology. 2002, Vol 9, Num 2, pp 133-139, issn 1065-6251Article

Les maladies héréditaires de la membrane érythrocytaire: du tableau clinique aux mécanismes génétiques et moléculaires sous-jacents = Hereditary diseases of erythrocyte membrane : from clinical aspects to underlying genetical and molecular mechanismsBICHIS, M; HUBER, A. R.Annales de biologie clinique (Paris). 2000, Vol 58, Num 3, pp 277-289, issn 0003-3898Article

4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosisPERROTTA, S; IOLASCON, A; POLITO, R et al.Haematologica - Journal of hematology. 1999, Vol 84, Num 7, pp 660-662Article

Induction of erythrocyte protein 4.2 gene expression during differentiation of murine erythroleukemia cellsKARACAY, B; CHANG, L.-S.Genomics (San Diego, Calif.). 1999, Vol 59, Num 1, pp 6-17, issn 0888-7543Article

Interleukin-6 and interleukin-11 act synergistically with thrombopoietin and stem cell factor to modulate ex vivo expansion of human CD41+and CD61+ megakaryocytic cellsLAZZARI, L; HENSCHLER, R; LECCHI, L et al.Haematologica (Roma). 2000, Vol 85, Num 1, pp 25-30, issn 0390-6078Article

Relationships between DNA methylation and expression in erythrocyte membrane protein (band 3, protein 4.2, and β-spectrin) genes during human erythroid development and differentiationREMUS, Ralph; KANZAKI, Akio; DOERFLER, Walter et al.International journal of hematology. 2005, Vol 82, Num 5, pp 422-429, issn 0925-5710, 8 p.Article

DNA methylation in promoter regions of red cell membrane protein genes in healthy individuals and patients with hereditary membrane disordersREMUS, Ralph; KANZAKI, Akio; DOERFLER, Walter et al.International journal of hematology. 2005, Vol 81, Num 5, pp 385-395, issn 0925-5710, 11 p.Article

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