Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jenny Cañizales"'
Autor:
Alicia Rojas-Atencio, Karelis Urdaneta, Marisol Soto-Quintana, Francisco Alvarez Nava, Jenny Cañizales, Ernesto Solis
Publikováno v:
Case Reports in Pathology, Vol 2011 (2011)
We report a case of acute basophilic leukemia with two coexisting clonal abnormalities, t(9;22) and trisomy 19. The blast showed positive reaction with myeloperoxidase but negative reaction with chloroacetate esterase and acid phosphatase. Metachroma
Externí odkaz:
https://doaj.org/article/0c1f92c77bbb4b0b904d0da7b14d444c
Autor:
Maribel Quintero, Alicia Rojas-Atencio, Ana Ruiz, Maczy González, Olga Briceño, Karelis Urdaneta, Melvis Arteaga-Vizcaino, Mirian Duertos, Jenny Cañizales
Publikováno v:
Saber, Vol 26, Iss 4, Pp 416-427 (2018)
Acute leukemias are malignant hematopoietic cells of immature proliferations of the blastic type, whose progressive accumulation is accompanied by a decrease in the production of normal myeloid elements. Transcription of inactive tumor suppressor gen
Autor:
Karelis Urdaneta, Ernesto Solís, Jenny Cañizales, Francisco Alvarez Nava, Alicia Rojas-Atencio, Marisol Soto-Quintana
Publikováno v:
Case Reports in Pathology, Vol 2011 (2011)
Case Reports in Pathology
Case Reports in Pathology
We report a case of acute basophilic leukemia with two coexisting clonal abnormalities, t(9;22) and trisomy 19. The blast showed positive reaction with myeloperoxidase but negative reaction with chloroacetate esterase and acid phosphatase. Metachroma
Autor:
María Caridad Martínez-Basalo, Richard González, Tatiana Pardo-Govea, Wilmer Delgado-Luengo, William Zabala-Fernández, María Luisa Hernández, Juana Delgado-Luengo, Lennie Pineda-Bernal, Ernesto Solís-Añez, Alisandra Morales-Machín, Lisbeth Borjas-Fuentes, Elizabeth M. Petty, Sandra González-Ferrer, Orlando Römel, Herminia Fleitas-Cabello, Karelis Urdaneta, Jenny Cañizales
Publikováno v:
American journal of medical genetics. Part A. (10)
A 10-year-old boy with manifestations of Petty–Laxova–Wiedemann progeroid syndrome (PLWPS), a rare neonatal progeroid condition, is described and compared with those previously reported. Clinical manifestation include: severe pre- and postnatal g
Autor:
Pedro, Estrada, Alicia, Rojas-Atencio, William, Zabala, Lisbeth, Borjas, Lazaro, Soca, Karelis, Urdaneta, Francisco, Alvarez-Nava, Jenny, Cañizales, Janeth, Rojas, Marisol, Soto
Publikováno v:
Investigacion clinica. 50(1)
Mutations in the K-ras oncogene are common in colo-rectal cancer, which affect the biological behaviour and may influence the susceptibility to therapy in these tumors. The objective of this work was to identify the types of K-ras mutations observed
Autor:
Ernesto, Solís-Añez, Wilmer, Delgado-Luengo, Lisbeth, Borjas-Fuentes, William, Zabala, Nailet, Arráiz, Lennie, Pineda, María Gabriela, Portillo, Sandra, González-Ferrer, José Antonio, Chacín, Joaquín, Peña, Cecilia, Montiel, Alisandra, Morales, Alicia, Rojas de Atencio, Jenny, Cañizales, Richard, González, Luis Eduardo, Miranda, Nivia, Abreu, Juana, Delgado
Publikováno v:
Investigacion clinica. 48(2)
Autism is a complex neurodevelopmental disorder characterized by impairment of social interaction, language, communication, and stereotyped, repetitive behavior. Genetic predisposition to Autism has been demonstrated in families and twin studies. The
Autor:
Marbenis, Díaz-Valecillos, Janice, Fernández, Alicia, Rojas, José, Valecillos, Jenny, Cañizales
Publikováno v:
Investigacion clinica. 45(3)
With the purpose of determining and characterizing chromosomal alterations and their relation to the radiation dose, time of employment and weekly exposure time, a transversal cut-descriptive study was performed on 18 workers, exposed to ionizing rad