Zobrazeno 1 - 10
of 30
pro vyhledávání: '"M T, Ducluzeau"'
Publikováno v:
ResearcherID
SummaryHeterozygous 4.1(−) hereditary elliptocytosis results from the absence of one haploid set of protein 4.1, a major component of the red cell skeleton. Two successive epidemiological investigations revealed fifteen probands in the French North
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413fd773812b5740badb03bdb42bbeb4
https://pubmed.ncbi.nlm.nih.gov/8478372
https://pubmed.ncbi.nlm.nih.gov/8478372
Autor:
N, Alloisio, R, Wilmotte, L, Morlé, F, Baklouti, J, Maréchal, M T, Ducluzeau, L, Denoroy, C, Féo, B G, Forget, R, Kastally
Publikováno v:
Blood. 80(3)
Spectrin Jendouba (alpha II/31) was found in a Tunisian family. In the heterozygous state, it is associated with asymptomatic elliptocytosis and a minimal defect in spectrin dimer self-association. On partial digestion of spectrin with trypsin, an ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45188364bd14625fb4e9801b23464f3c
https://pubmed.ncbi.nlm.nih.gov/1638030
https://pubmed.ncbi.nlm.nih.gov/1638030
Autor:
F, Baklouti, J, Maréchal, R, Wilmotte, N, Alloisio, L, Morlé, M T, Ducluzeau, L, Denoroy, A, Mrad, M H, Ben Aribia, R, Kastally
Publikováno v:
Blood. 79(9)
Elliptocytogenic alpha I/36 spectrin Sfax is a new variant found in a Tunisian family. The alpha I/36 allele yielded a clinically manifest picture only when occurring in trans to a recently identified, low expression level polymorphism referred to as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::382d1dd11fff66c202d2095b61452898
https://pubmed.ncbi.nlm.nih.gov/1571558
https://pubmed.ncbi.nlm.nih.gov/1571558
Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps
Autor:
S, Feddal, G, Brunet, L, Roda, S, Chabanis, N, Alloisio, L, Morlé, M T, Ducluzeau, J, Maréchal, J M, Robert, E J, Benz
Publikováno v:
Blood. 78(8)
4.1(-) hereditary elliptocytosis (HE) is a variety of elliptocytosis resulting from the reduction (heterozygosity) or the absence (homozygosity) of protein 4.1. It is nearly always encountered in its heterozygous form. It has been found among Caucasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a41d6313a3682de23d0b908f0839e586
https://pubmed.ncbi.nlm.nih.gov/1912588
https://pubmed.ncbi.nlm.nih.gov/1912588
Autor:
B, Pothier, N, Alloisio, J, Maréchal, L, Morlé, M T, Ducluzeau, C, Caldani, N, Philippe, J, Delaunay
Publikováno v:
Blood. 75(10)
Partial digestion of spectrin dimers in vitro has allowed the definition of domains. For example, the portions of the dimers that are involved in spectrin self-association are represented by the alpha I and the beta I domains. The alpha I domain (80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c08f52490467d608f52339002f821185
https://pubmed.ncbi.nlm.nih.gov/2337674
https://pubmed.ncbi.nlm.nih.gov/2337674
Autor:
N, Alloisio, D, Guetarni, L, Morlé, B, Pothier, M T, Ducluzeau, A, Soun, P, Colonna, M, Clerc, N, Philippe, J, Delaunay
Publikováno v:
American journal of hematology. 23(2)
The Sp alpha I/65 variant of the spectrin has been recently described in black people with hereditary elliptocytosis (HE). The present study reports on a similar Sp alpha I/65 variant in nine North African persons belonging to four unrelated families
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03005a3c853d05f340b40ac29aec5adb
https://pubmed.ncbi.nlm.nih.gov/3752066
https://pubmed.ncbi.nlm.nih.gov/3752066
Autor:
B, Pothier, L, Morlé, N, Alloisio, M T, Ducluzeau, C, Caldani, C, Féo, M, Garbarz, I, Chaveroche, D, Dhermy, M C, Lecomte
Publikováno v:
Blood. 69(6)
We describe a new spectrin variant with a truncated beta-chain. It was discovered in a 17-year-old white boy presenting with intermittent jaundice and spleen enlargement. He also displayed numerous smooth elliptocytes. On sodium dodecyl sulfate-polya
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef610962079ef5108a7ed7a6f1ccf88b
https://pubmed.ncbi.nlm.nih.gov/3580577
https://pubmed.ncbi.nlm.nih.gov/3580577
Publikováno v:
Blood. 71(2)
Spectrin Tunis (alpha 1/78) was found in the heterozygous state in a young white North-African man and his mother. Both of them presented with mild elliptocytosis. Using one-dimensional electrophoresis, a sharp 78 kd fragment was present with a recip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c69ea83b4614dbf74f6eeaa4114b432c
https://pubmed.ncbi.nlm.nih.gov/3337911
https://pubmed.ncbi.nlm.nih.gov/3337911
Autor:
N, Alloisio, L, Morlé, B, Pothier, A F, Roux, J, Maréchal, M T, Ducluzeau, Z, Benhadji-Zouaoui, J, Delaunay
Publikováno v:
Blood. 71(4)
We report on spectrin Oran (alpha II/21), a new spectrin variant found in an Algerian family. It was characterized by the absence of the spots that classically correspond to the alpha II domain using two-dimensional analysis of spectrin limit digests
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00c37c6e68932a2dd5ae6b96de319193
https://pubmed.ncbi.nlm.nih.gov/2895677
https://pubmed.ncbi.nlm.nih.gov/2895677