Výsledky vyhledávání - "J M, de Pablos"

Akademický článek

Reseña de 'Infoperiodismo: la visión' de J. M. de Pablos'

Autor: José Álvarez Marcos

Publikováno v: Ámbitos, Iss 4, Pp 329-330 (2000)

Externí odkaz: https://doaj.org/article/07c142cb49e049d18b8f34253001fb72

Molecular and flow cytometry characterization during the follow-up of three simultaneous lymphoproliferative disorders: Hairy cell leukemia, monoclonal B-cell lymphocytosis, and CD4++/CD8+/−dim T-large granular lymphocytosis-A case report

Autor: Manuel Almagro, P. López, C. Sánchez, Marcos González, Pilar Garrido, Cabrera A, Pilar Jiménez, Manuel Jurado, Pilar Navarro, F. Valero, J. M. de Pablos, Francisco Ruiz-Cabello, Ana Balanzategui

Publikováno v: Cytometry Part B: Clinical Cytometry. :195-200

The simultaneous diagnosis of hairy cell leukemia and monoclonal B-cell lymphocytosis with the characteristics of “indolent” chronic lymphocytic leukemia is rare but not unknown. However, an association with a third clonal lymphoproliferative dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d627d3953a4c90fe50112a9a52eaf029
https://doi.org/10.1002/cyto.b.20579

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Hb Fannin-Lubbock in Five Spanish Families is Characterized by two Mutations: β111 GTC->CTC (VAL->LEU) AND β119 GGC->GAC (GLY->ASP)

Autor: J. B. Wilson, J. M. De Pablos, D. D. Pobedimskaya, W.-B. Qin, Titus H.J. Huisman, L.-H. Gu, T. P. Molchanova

Publikováno v: Hemoglobin. 18:297-306

We have sequenced the amplified beta-globin genes of five, apparently unrelated, Spanish adults with a fast-moving hemoglobin variant, and observed a GGC-->GAC mutation at codon 119 which identified the abnormality as Hb Fannin-Lubbock or alpha 2 bet

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9b35920b508a6a350d7e7f792b534575
https://doi.org/10.3109/03630269408996195

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Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions

Autor: I Rodriguez, Ferdane Kutlar, Brooke B. Webber, J. B. Wilson, JT Prchal, J. F. Codrington, J. M. De Pablos, Abdullah Kutlar, H. Hu, KM Hall

Publikováno v: Blood. 75:1883-1887

Two unstable hemoglobins (Hbs) causing rather severe hemolytic anemia have been characterized. The beta chain of Hb Birmingham, found in an adult black man, is characterized by the loss of -Leu-Ala-His-Lys- at positions 141, 142, 143, and 144 and the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::863c73306e999cc7a536fc8b0f70b3f2
https://doi.org/10.1182/blood.v75.9.1883.bloodjournal7591883

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Use of rhG-CSF in the collection of peripheral blood stem cells for autologous blood stem cell transplantation in acute myeloblastic leukemia

Autor: M, Jurado, C, Delgado, A, Moratalla, D, Casero, S, Oyonarte, J M, de Pablos

Publikováno v: Bone marrow transplantation. 18(4)

The use of recombinant granulocyte colony-stimulating factor (rhG-CSF) alone is attractive for the collection of peripheral blood stem cells (PBSC) in several malignancies. In acute myeloblastic leukemia (AML), not enough experience has been gained w

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c10b5cce0007854f5fc35e3a18480df1
https://pubmed.ncbi.nlm.nih.gov/8899205

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Hb Anamosa or alpha 2(111)(G18)Ala--Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala--Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected by sequencing of amplified DNA

Autor: E G, Kazanetz, J Y, Leonova, J B, Wilson, S K, McMillan, M, Walbrecht, J M, de Pablos Gallego, T H, Huisman

Publikováno v: Hemoglobin. 19(1-2)

We have identified silent amino acid substitutions in two alpha chain variants present in families from Iowa, USA, and Granada, Spain. Both involve an alanine residue in the core peptide, namely Ala--Val at position 111 (codon change in the alpha 2 g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8dd1ca2a041d532a7ce3db4c366472d0
https://pubmed.ncbi.nlm.nih.gov/7615398

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