Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rosa María Arana-Trejo"'
Autor:
Rocio Ortiz-Lopez, Guillermo J. Ruiz-Delgado, Guillermo J. Ruiz-Argüelles, Jorge Cuervo-Sierra, Ramón Alejandro Martínez-Hernández, Cesar Daniel Villarreal-Villarreal, Gregorio Ignacio-Ibarra, Gabriel Muciño-Hernández, Javier Garcés-Eisele, Rosa María Arana-Trejo, Angélica María Jiménez-Mejía, Mónica Sánchez-Cárdenas, Gonzalo Vásquez-Palacio, José Carlos Jaime-Pérez, Julia Lutz-Presno, David Gómez-Almaguer, Ricardo Daniel García-Sepúlveda
Publikováno v:
Archives of Medical Research. 47:172-179
Background and Aims FLT3-ITD mutations in acute myeloid leukemia (AML) are associated with a poor prognosis. In Latin America, little epidemiological data exist about these mutations and their influence on clinical evolution and prognosis. Standardiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61fc07c362b6b0de0000b9acf9ef126b
https://doi.org/10.1016/j.arcmed.2016.06.003
https://doi.org/10.1016/j.arcmed.2016.06.003
Autor:
Hector Mayani, Jorge Vela-Ojeda, Elizabeth Sánchez-Valle, Antonieta Chávez-González, Elizabeth Ruiz-Sánchez, Rosa María Arana-Trejo, Manuel Ayala-Sánchez
Publikováno v:
Leukemia Research. 30:286-295
In this study, we have assessed the in vitro growth of hematopoietic progenitor cells (HPC) from chronic myeloid leukemia (CML) patients that have recovered after different treatments. Bone marrow cells were obtained from 33 CML patients, including p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b0e2c64b2fe6eaa5c84fa5b14029da
https://doi.org/10.1016/j.leukres.2005.06.028
https://doi.org/10.1016/j.leukres.2005.06.028
Autor:
Eugenia Flores-Figueroa, Juan José Montesinos, Hector Mayani, Rosa María Arana-Trejo, Guillermo Gutiérrez-Espı́ndola
Publikováno v:
Leukemia Research. 26:677-686
In vitro studies on the functional integrity of the hematopoietic microenvironment in myelodysplasia have been controversial. Although some of them suggest that such a microenvironment is functionally normal, there is increasing evidence indicating t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988b4b7614f79cdcdd9d73f3b3d5e03b
https://doi.org/10.1016/s0145-2126(01)00193-x
https://doi.org/10.1016/s0145-2126(01)00193-x
Autor:
Oscar Perez, Monica Tejeda, Israel Saldivar, Alberto Artristian, Rosa María Arana-Trejo, Maria-Paula Hernández, Raquel Amador-Sánchez, Yolanda Lugo, Gregorio Ignacio, Juan-Carlos Solís-Poblano, Jorge Cruz-Rico, Luis Solís-Anaya
Publikováno v:
Blood. 128:5273-5273
The Ph chromosome is a translocation (9;22)(q34;q11), that results in the constitutive activation of the BCR/ABL tyrosine kinase. The incidence of BCR/ABL in Acute Lymphoblastic Leukemia (ALL) increases with age, from less than 5% in younger children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::336a6a43a18c0d73dda54748c58f0c39
https://doi.org/10.1182/blood.v128.22.5273.5273
https://doi.org/10.1182/blood.v128.22.5273.5273
Autor:
Elizabeth Sánchez-Valle, Enrique Gómez-Morales, Hector Mayani, Rosa María Arana-Trejo, Miguel Angel Castro, Guadalupe Martínez-Jaramillo, Ignacio Valencia-Plata, Pizzuto-Chávez J
Publikováno v:
American Journal of Hematology. 59:149-155
By using Dexter-type long-term marrow cultures (D-LTMC), it has been shown previously that hematopoietic progenitor cells (H PC) from patients with aplastic anemia (AA) have a deficient proliferation in vitro. The studies reported to date, however, h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beb0de6519a93e335d5b9b29df4a704f
https://doi.org/10.1002/(sici)1096-8652(199810)59:2<149::aid-ajh8>3.0.co
https://doi.org/10.1002/(sici)1096-8652(199810)59:2<149::aid-ajh8>3.0.co
Autor:
Hector Mayani, Erika Hernández-Estévez, Patricia Flores-Guzmán, Eugenia Flores-Figueroa, Sebastian Castillo-Medina, Adrián Pérez-Cabrera, Juan José Montesinos, Guillermo Gutiérrez-Espı́ndola, Rosa María Arana-Trejo, Lourdes Arriaga
Publikováno v:
Leukemia research. 32(9)
Two different reports, including one from our own group, have recently demonstrated the presence of severe chromosomal abnormalities in mesenchymal stem cells (MSC) from patients with myelodysplastic syndromes (MDS). In the present study, we have ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97243f34af1569d328d6fc0c7dcee405
https://pubmed.ncbi.nlm.nih.gov/18405968
https://pubmed.ncbi.nlm.nih.gov/18405968
Autor:
Hector Mayani, Maria Antonieta Vélez-Ruelas, Guadalupe Martínez-Jaramillo, Rosa María Arana-Trejo
Publikováno v:
Hematology (Amsterdam, Netherlands). 11(5)
Fanconi anemia (FA) is a rare autosomal recessive disorder characterized by bone marrow (BM) failure and a wide array of physical abnormalities. Around 9% of FA patients develop acute myeloid leukemia (AML), which makes FA a good genetic model to stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d9f17d545156b654e4dea4aec371267
https://pubmed.ncbi.nlm.nih.gov/17607582
https://pubmed.ncbi.nlm.nih.gov/17607582
Autor:
Eugenia Flores-Figueroa, Guillermo Gutiérrez-Espı́ndola, Adrián Pérez-Cabrera, Rosa María Arana-Trejo, Hector Mayani
Publikováno v:
Leukemia research. 29(2)
Bone marrow-derived mesenchymal stem cells (MSC) have been defined as primitive, undifferentiated cells, capable of self-renewal and with the ability to give rise to different cell lineages, including adipocytes, osteocytes, fibroblasts, chondrocytes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f359febcf33a3999e5a357d2e15977f
https://pubmed.ncbi.nlm.nih.gov/15607371
https://pubmed.ncbi.nlm.nih.gov/15607371
Autor:
Angélica María Jiménez-Mejía, Jorge Cuervo-Sierra, Mónica Sánchez-Cárdenas, José Carlos Jaime-Pérez, Guillermo J. Ruiz-Argüelles, Gabriel Muciño-Hernández, David Gómez-Almaguer, Ramón Alejandro Martínez-Hernández, Gonzalo Vásquez-Palacio, Julia Lutz-Prestno, Mauricio Camargo-Guerrero, Guillermo J. Ruiz-Delgado, Ricardo David García Sepúlveda, Rosa María Arana-Trejo, Gregorio Ignacio-Ibarra, Rocio Ortiz-Lopez
Publikováno v:
Blood. 122:4979-4979
In acute myeloid leukemia (AML), FLT3 mutations are associated with a poor prognosis, particularly the internal tandem duplication (ITD/FLT3). In Latin America there are few epidemiological data about these mutations.This study assessed the prevalenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d2df39c384cb0e008451005d0529d0d
https://doi.org/10.1182/blood.v122.21.4979.4979
https://doi.org/10.1182/blood.v122.21.4979.4979
Autor:
Carlos Váldez, Samuel Celestino, Gregorio Ignacio, Jesus Elias Castellanos, Ramón Rivas, Veronica D. Gonzalez, Maria Paula Hérnandez, Luis Solis, Rosa María Arana-Trejo, Yolanda Lugo
Publikováno v:
Blood. 118:5180-5180
Abstract 5180 Introduction: The V617F mutation in JAK2 gene has been described in approximately 50–90% of patients with ET, MF AND PV [essential trombocythaemia, idiopathic myelofibrosis and policithemia vera]; but has also been reported, albeit at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16d01a11f296d0de62107cd76615689e
https://doi.org/10.1182/blood.v118.21.5180.5180
https://doi.org/10.1182/blood.v118.21.5180.5180