Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Celsa Quinteiro"'
Publikováno v:
PLoS ONE, Vol 4, Iss 4, p e5174 (2009)
The kings of the Spanish Habsburg dynasty (1516-1700) frequently married close relatives in such a way that uncle-niece, first cousins and other consanguineous unions were prevalent in that dynasty. In the historical literature, it has been suggested
Externí odkaz:
https://doaj.org/article/7ac63b0f7ed047149d9a13463267d6a0
Publikováno v:
PLoS ONE, Vol 3, Iss 5, p e2138 (2008)
The systematic study of the human genome indicates that the inter-individual variability is greater than expected and it is not only related to sequence polymorphisms but also to gene copy number variants (CNVs). Congenital Adrenal Hyperplasia due to
Externí odkaz:
https://doaj.org/article/c9bb0f5c86f44a3b8c81da30aeff1c55
Autor:
Beatriz Bellosillo Paricio, Alberto Álvarez Larrán, Szukalski Łukasz, Marcio Andrade-Campos, Maria Laura Fox, Aitor Abuin Blanco, Celsa Quinteiro García, Jesús María González Martín, Alejandro Martín Martín, Anna Czyż, Manuel Mateo Pérez Encinas, K Lewandowki, Elena Magro Mazo, Juan Carlos Hernandez Boluda, Aleksandra Gołos, Mercedes Gasior Kabat, María Soledad Noya Pereira, Ruth Stuckey, María Teresa Gómez-Casares, Francisca Ferrer-Marín, José María Raya, Marta Sobas
Publikováno v:
EUROPEAN JOURNAL OF HAEMATOLOGY
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
OBJECTIVES: In patients with essential thrombocythemia (ET), after the JAK2V617F driver mutation, mutations in CALR are common (classified as type-1, 52-bp deletion, or type-2, 5-bp insertion). CALR mutations have generally been associated with a low
Autor:
María J. García-Barchino, Celsa Quinteiro, Manuel Pérez-Encinas, José L. Vizmanos, M. García-Delgado, Francisco J. Novo, Sara Labiano, Mikhail Shugay, Elisa M. Salas
Publikováno v:
Genes & Cancer. 2:593-596
A search for genes potentially regulated by STAT5 identified leukemia inhibitory factor (LIF) as a good candidate. Using various experimental approaches, we have validated LIF as a direct transcriptional target of STAT5 in myeloid cell lines: STAT5 b
Autor:
Tatjana Zabelina, Reyad Dada, Akitoshi Nagasaki, Alice Santos-Silva, Stefan Wilop, A. Palmieri, Hwei-Fang Tien, Celsa Quinteiro García, Jung Lim Lee, D. Cilloni, Maite Hartwig, Seok Kim, G. Saglio, S. Carturan, Francis Ayuk, Sang Kyun Sohn, Susana Rocha, V. Formica, Nobuyuki Takasu, Jong Weon Choi, Byung Soo Kim, Ho Jin Shin, Jung Hye Kwon, Sunghyun Kim, Young Rok Do, Seong Kyu Park, Edgar Jost, D. Cunningham, Dorine W. Swinkels, Hawk Kim, Jeong Hee Kim, Coby M. Laarakkers, Nicolaus Kröger, Gyeong-Won Lee, A. Wotherspoon, Axel R. Zander, Joon Seong Park, Ulrike Bacher, E. Messa, Marta Sobas, G. Chong, Jae Hoon Lee, Chul Soo Kim, Frederico Teixeira, Jong-Ho Won, Hye Jin Kang, Nikolaus Gassler, R.M. Pellegrino, Chang-Ki Min, Tsung-Yu Lan, Cheolwon Suh, Bong-Seog Kim, Hyunchoon Shin, Sung-Soo Yoon, Flávio Reis, María J. Rabuñal Martinez, Svetlana Asenova, Moon Whan Im, Manuel Mateo Pérez Encinas, Rong-Sen Yang, Hyeon-Seok Eom, Deog-Yeon Jo, J. Oates, A. Roetto, Young-Don Joo, Sukjoong Oh, Ho Young Kim, Min Kyoung Kim, Jin Seok Kim, Moon Hee Lee, Yeung-Chul Mun, Christine M. Seroogy, Yang Soo Kim, Chong Won Park, Petronila Rocha-Pereira, Bettina Wiedemann, Karl Wu, Taeko Okudaira, Rainhardt Osieka, Hyeok Shim, Dong-Tsamn Lin, Oliver Galm, José Luis Bello López, Takashi Miyagi, Maria do Sameiro Faria, Je-Jung Lee, Atsushi Yamanoha, Debra A. MacKenzie, Jae-Yong Kwak, Alfredo Loureiro, Luís Belo, Chih-Yu Chen, Dong Soon Lee, Vasco Miranda, Sunday Ocheni, Hun-Mo Ryoo, Hwi-Joong Yoon, Soo Mee Bang, Hartmut Kabisch, A.R. Norman, Rudolf Erttmann, Alexandre Quintanilha, Hyo Jung Kim, Elísio Costa, Jong-Youl Jin, Ki-Hyun Kim
Publikováno v:
Acta Haematologica. 122:I-IV
Autor:
Wiebke Arlt, Celsa Quinteiro, Lourdes Loidi, Felix G. Riepe, Caroline Bleicken, Fernando Domínguez, Nils Krone, Silvia Parajes, Wolfgang G. Sippell, Joachim Grötzinger, Vivek Dhir
Publikováno v:
Human Mutation. 30:E443-E450
Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase (CYP21A2) deficiency is the commonest inborn error in steroid hormone biosynthesis. Functional in vitro assessment of mutant activity generally correlates well with clinical phenotype
Publikováno v:
Alcoholism: Clinical and Experimental Research. 30:7-14
Background: Serum IgE is increased in heavy drinkers. Endotoxin mediates most of the immunological alterations associated with heavy drinking. The −159C/T polymorphism in the promoter region of the gene encoding CD14 (an endotoxin receptor) is asso
Autor:
Arturo Gonzalez-Quintela, Celsa Quinteiro, Jose-Antonio Torre, Carmen Vidal, Luis-Fernando Perez, Francisco Gude, Joaquin Campos
Publikováno v:
Alcoholism: Clinical & Experimental Research. 29:1206-1213
Background: Innate inflammatory responses to endotoxin (lipopolysaccharide) contribute to the development of alcoholic liver disease (ALD). A single-nucleotide polymorphism (−159C/T) in the promoter region of the gene coding for CD14 (a lipopolysac
Autor:
Mónica Marazuela, Tomás Lucas, Purificación Martínez de Icaya, Celsa Quinteiro, Cristina Álvarez-Escolá, Paz de Miguel, Isabel Pavón, Concepción Blanco, Ignacio Bernabeu, Javier Riveiro, Ana M. Ramos-Leví, Amalia Paniagua
Publikováno v:
European journal of endocrinology. 172(2)
ObjectiveIGF1 and IGFBP3 gene polymorphisms have been recently described. However, their potential role in the setting of acromegaly and its outcome is unknown. In this study, we analyze these polymorphisms in patients with acromegaly and investigate
Autor:
Felipe F. Casanueva, Paula Andujar-Plata, Celsa Quinteiro, Ignacio Bernabeu, E. Fernández-Rodríguez
Publikováno v:
Endocrine Abstracts.