Zobrazeno 1 - 10
of 310
pro vyhledávání: '"D Dhermy"'
Autor:
I. Florent, S. Le Bonniec, B. Carcy, P. Grellier, O. Mercereau-Puijalon, S. Bonnefoy, D. Dhermy, M. Monsigny, R. Mayer, J. Schrével
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 89, Pp 47-49 (1994)
Numerous proteinase activities have been shown to be essential for the survival of Plasmodium falciparum. One approach to antimalarial chemotherapy, would be to block specifically one or several of these activities, by using compounds structurally an
Externí odkaz:
https://doaj.org/article/409d5d24aa7d40b8b930f267ff7a92ad
Autor:
D Dhermy, ME dos Santos, M. Bozon, J. Delaunay, P Texier, D Drenckhahn, Nicole Alloisio, S. Hayette, L Morle
Publikováno v:
Blood. 85:250-256
We studied a 26-year-old Portuguese patient with recessively transmitted hereditary hemolytic anemia. Protein 4.2 was absent from red cell ghosts by Western blotting. Although the 4.2 mRNA was not detected in Northern blots, it was shown to be presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86da30bf812078ae5f2e28c787fde7b3
https://doi.org/10.1182/blood.v85.1.250.bloodjournal851250
https://doi.org/10.1182/blood.v85.1.250.bloodjournal851250
Publikováno v:
European Journal of Pediatrics. 158:628-630
Portal vein thrombosis is a rare but potentially lethal complication in children requiring splenectomy. We report on a 15-year-old boy with a dehydrated hereditary stomatocytosis, who underwent splenectomy and presented a postoperative partial portal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::711f3a03a71190c1b8c654e22787c028
https://doi.org/10.1007/s004310051165
https://doi.org/10.1007/s004310051165
Publikováno v:
International Journal of Biochemistry. 22:1479-1489
1. 1. In whole ghosts, ankyrin, protein 4.1, protein band 3 and spectrin are lysed by purified calpain I in the presence of calcium. 2. 2. Limited calpain lysis of purified ankyrin results in several peptides, including a 85 kD peptide bearing the an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319f637c43f8fd5df1c760a4d788b950
https://doi.org/10.1016/0020-711x(90)90240-4
https://doi.org/10.1016/0020-711x(90)90240-4
Autor:
B. Carcy, Serge Bonnefoy, Isabelle Florent, S L Le Bonniec, Michel Monsigny, Philippe Grellier, D. Dhermy, Roger Mayer, Odile Mercereau-Puijalon, Joseph Schrével
Publikováno v:
Memórias do Instituto Oswaldo Cruz., Vol 89, Pp 47-49 (1994)
Memórias do Instituto Oswaldo Cruz, Volume: 89 Supplement 2, Pages: 47-49, Published: 1994
Memórias do Instituto Oswaldo Cruz, Volume: 89 Supplement 2, Pages: 47-49, Published: 1994
Numerous proteinase activities have been shown to be essential for the survival of Plasmodium falciparum. One approach to antimalarial chemotherapy, would be to block specifically one or several of these activities, by using compounds structurally an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5049a9c3f926be3074e56f9dcd151b07
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761994000600012
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761994000600012
Publikováno v:
Clinical and laboratory haematology. 22(6)
We studied a recessive hereditary spherocytosis (HS) family from Norway in which all four children had haemolytic spherocytosis while spectrin (Sp) deficiency was detected in the proband. Molecular analysis demonstrated that all affected children had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::438dd7a96c29614b2a2ad9a618202c0d
https://pubmed.ncbi.nlm.nih.gov/11318798
https://pubmed.ncbi.nlm.nih.gov/11318798
Autor:
S, Grootenboer, P O, Schischmanoff, I, Laurendeau, T, Cynober, G, Tchernia, J P, Dommergues, D, Dhermy, M, Bost, B, Varet, M, Snyder, S K, Ballas, B, Ducot, M C, Babron, G W, Stewart, P, Gasparini, A, Iolascon, J, Delaunay
Publikováno v:
Blood. 96(7)
Dehydrated hereditary stomatocytosis (DHS) is a rare genetic disorder of red cell permeability to cations, leading to a well-compensated hemolytic anemia. DHS was shown previously to be associated in some families with a particular form of perinatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7acc85b21af06836e3e23252e334d3e4
https://pubmed.ncbi.nlm.nih.gov/11001917
https://pubmed.ncbi.nlm.nih.gov/11001917
Publikováno v:
Blood. 89(12)
An alpha-spectrin variant with increased susceptibility to tryptic digestion, alpha(II/47), was previously observed in a child with severe, recessively inherited, poikilocytic anemia. The molecular basis of this variant, spectrin St Claude, has now b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::10ffcd1ce424ea67fad6b39aa73d7d11
https://pubmed.ncbi.nlm.nih.gov/9192783
https://pubmed.ncbi.nlm.nih.gov/9192783
Autor:
S L, Le Bonniec, C, Fournier, C, Deregnaucourt, P, Grellier, D, Dhermy, M C, Lecomte, J, Schrevel
Publikováno v:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie. 319(11)
Many proteases play a crucial role in the Plasmodium intraerythrocytic life cycle. Spectrin depletion, one of the major events involved in parasite release from the red blood cell, results from proteolytic activities associated with the presence of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1feedb7cbef9b0d128cad068db0ce83
https://pubmed.ncbi.nlm.nih.gov/9033845
https://pubmed.ncbi.nlm.nih.gov/9033845
Publikováno v:
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie. 319(10)
Hereditary spherocytosis (HS) is an inherited hemolytic anemia characterized by the presence of dense spherocytic red cells. In HS patients, red cell membrane protein gel electrophoresis has identified different subsets of abnormalities: isolated spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d4db9c44dda02e05965894a1d72585c2
https://pubmed.ncbi.nlm.nih.gov/8977772
https://pubmed.ncbi.nlm.nih.gov/8977772