Zobrazeno 1 - 10
of 88
pro vyhledávání: '"B G, Forget"'
Publikováno v:
Blood. 82:2210-2215
Hereditary elliptocytosis (HE) is a heterogeneous disorder of red blood cells frequently associated with abnormal limited tryptic digestion of the alpha I domain of spectrin and impaired spectrin dimer self- association. We studied two related indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91636d79644ea6ddbc99476d845e9515
https://doi.org/10.1182/blood.v82.7.2210.bloodjournal8272210
https://doi.org/10.1182/blood.v82.7.2210.bloodjournal8272210
Autor:
N L Lumelsky, B G Forget
Publikováno v:
Molecular and Cellular Biology. 11:3528-3536
The human erythroleukemic cell line K562 was used as a model for analysis of the mechanisms responsible for alterations in gene expression during differentiation. K562 cells normally synthesize fetal hemoglobin (gamma-globin), but treatment with tumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67bb7e98df97d30a4d7ae523240e5665
https://doi.org/10.1128/mcb.11.7.3528
https://doi.org/10.1128/mcb.11.7.3528
Publikováno v:
European journal of haematology. 67(2)
The precise role of hematopoietic cytokine/cytokine receptor interactions in lineage-restricted hematopoietic differentiation giving rise to mature blood cells of diverse function is incompletely defined. To study lineage-specific effects of cytokine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29355f01d08992a833d34e2b53a1f108
https://pubmed.ncbi.nlm.nih.gov/11722594
https://pubmed.ncbi.nlm.nih.gov/11722594
Publikováno v:
Transactions of the American Clinical and Climatological Association. 111
We studied a kindred with dominantly inherited familial erythrocytosis associated with heterozygosity for a deletion of seven nucleotides in exon 8 of the EpoR gene resulting in an EpoR peptide that is truncated by 59 amino acids in its C-terminal in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07d097ea4228479dfb2cf5d269e9b3aa
https://pubmed.ncbi.nlm.nih.gov/10881330
https://pubmed.ncbi.nlm.nih.gov/10881330
Publikováno v:
Blood. 92(4)
The role of hematopoietic growth factors in lineage commitment and differentiation is unclear. We present evidence that heterologous expression of an erythroid specific receptor allows granulocytic differentiation of a myeloid cell line. We have prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29b608857422819fde4e7e6392c4bc5d
https://pubmed.ncbi.nlm.nih.gov/9694710
https://pubmed.ncbi.nlm.nih.gov/9694710
Publikováno v:
American journal of hematology. 56(2)
Defects of alpha spectrin have been identified in many cases of hereditary elliptocytosis (HE) and hereditary pyropoikilocytosis (HPP). To aid in the genetic analysis of families with these disorders, the locations of three alpha-spectrin gene polymo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::906915589ee0dd6b41832217360fdbc4
https://pubmed.ncbi.nlm.nih.gov/9326352
https://pubmed.ncbi.nlm.nih.gov/9326352
Publikováno v:
The Journal of biological chemistry. 272(31)
Ankyrin-1 (ANK-1) is an erythrocyte membrane protein that is defective in many patients with hereditary spherocytosis, a common hemolytic anemia. In the red cell, ankyrin-1 provides the primary linkage between the membrane skeleton and the plasma mem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b01a9d3990cae2e9a51ebf0468a3f8db
https://pubmed.ncbi.nlm.nih.gov/9235914
https://pubmed.ncbi.nlm.nih.gov/9235914
Publikováno v:
Blood. 89(12)
Familial erythrocytosis (familial polycythemia) inherited as an autosomal dominant trait has recently been reported to be associated with mutations in the gene encoding the erythropoietin receptor (EpoR) in a small number of families. We studied a ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c12774e4931740c5e4bee676cce7d1c
https://pubmed.ncbi.nlm.nih.gov/9192789
https://pubmed.ncbi.nlm.nih.gov/9192789
Autor:
L, Morlé, M, Bozon, N, Alloisio, A, Vallier, S, Hayette, O, Pascal, D, Monier, N, Philippe, B G, Forget, J, Delaunay
Publikováno v:
American journal of hematology. 54(3)
We describe a case of spherocytosis in a French child splenectomized at age 10 years. The parents were devoid of any clinical, hematological, or biochemical abnormalities. Following splenectomy, the proposita exhibited a reduction of red cell membran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6bd65c034d09642f6d99bf6cc87a87f
https://pubmed.ncbi.nlm.nih.gov/9067504
https://pubmed.ncbi.nlm.nih.gov/9067504
Autor:
W T, Tse, P G, Gallagher, P B, Jenkins, Y, Wang, L, Benoit, D, Speicher, J C, Winkelmann, P, Agre, B G, Forget, S L, Marchesi
Publikováno v:
American journal of hematology. 54(3)
Nondominant hereditary spherocytosis (ndHS) is a disorder characterized in some patients by severe hemolytic anemia and marked deficiency of erythrocyte spectrin. This report describes the identification of a variant spectrin chain, alpha-spectrin Bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7f4553c83bda81a4af994afaeca8a14a
https://pubmed.ncbi.nlm.nih.gov/9067503
https://pubmed.ncbi.nlm.nih.gov/9067503