PUBLICACIONES DEL IBGM EN EL AÑO 2013

(en revistas indexadas en PubMed)

Fisiología Celular y Molecular (CMP)

Orozco L, Munar A, Soler R, Alberca M, Soler F, Huguet M, Sentís J, Sánchez A, García-Sancho J.2013. Treatment of knee osteoarthritis with autologous mesenchymal stem cells: a pilot study. Transplantation 95: 1535-1541. Q1.

Quintero M, Gonzalez-Martin MC, Vega-Agapito V, Gonzalez C, Obeso A, Farré R, Agapito T, Yubero S. 2013. The effects of intermittent hypoxia on redox status, NF-κB activation, and plasma lipid levels are dependent on the lowest oxygen saturation. Free Radic. Biol. Med. 65: 1143-1154. Q1, D1.   

Ribeiro MJ, Sacramento JF, Gonzalez C, Guarino MP, Monteiro EC, Conde SV. 2013 Carotid body denervation prevents the development of insulin resistance and hypertension induced by hypercaloric diets. Diabetes 62: 2905-2916. Q1,D1 .

de la Fuente S, Fonteriz RI, Montero M, Alvarez J.2013. Ca2+ homeostasis in the endoplasmic reticulum measured with a new low-Ca²⁺-affinity targeted aequorin. Cell Calcium 54: 37-45. Q1.

Tajada S, Cidad P, Colinas O, Santana LF, Lopez-Lopez JR, Pérez-García T.2013. Down-regulation of CaV1.2 channels during hypertension: How fewer CaV1.2 channels allow more Ca2+ into hypertensive arterial smooth muscle. J. Physiol. 591: 6175-6191. Q1.

Muñoz E, Hernández-Morales M, Sobradillo D, Rocher A, Núñez L, Villalobos C.2013. Intracellular Ca²⁺ remodeling during the phenotypic journey of human coronary smooth muscle cells. Cell Calcium 54: 375-385. Q1.

Visiedo F, Bugatto F, Sánchez V, Cózar-Castellano I, Bartha JL, Perdomo G.2013. High glucose levels reduce fatty acid oxidation and increase triglyceride accumulation in human placenta. Am. J. Physiol. Endocrinol. Metab. 305: E205-E212. Q1, D1.

López-Acosta JF, Moreno-Amador JL, Jiménez-Palomares M, Díaz-Marrero AR, Cueto M, Perdomo G, Cózar-Castellano I.2013. Epoxypukalide induces proliferation and protects against cytokine-mediated apoptosis in primary cultures of pancreatic β-cells. PLoS One 8: e52862. Q1,D1.

Ramos-Rodriguez JJ, Ortiz O, Jimenez-Palomares M, Kay KR, Berrocoso E, Murillo-Carretero MI, Perdomo G, Spires-Jones T, Cozar-Castellano I, Lechuga-Sancho AM, Garcia-Alloza M.2013. Differential central pathology and cognitive impairment in pre-diabetic and diabetic mice. Psychoneuroendocrinology 38: 2462-2475. Q1,D1.

Pla-Martín D, Rueda CB, Estela A, Sánchez-Piris M, González-Sánchez P, Traba J, de la Fuente S, Scorrano L, Renau-Piqueras J, Alvarez J, Satrústegui J, Palau F.2013. Silencing of the Charcot-Marie-Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca²⁺ entry. Neurobiol. Dis. 55: 140-151. Q1,D1.

Inmunidad Innata e Inflamación (I3U)

Municio C, Alvarez Y, Montero O, Hugo E, Rodríguez M, Domingo E, Alonso S, Fernández N, Crespo MS.2013. The response of human macrophages to β-glucans depends on the inflammatory milieu. PLoS One 8: e62016. Q1,D1.

de la Puerta ML, Trinidad AG, Rodríguez MC, de Pereda JM, Sánchez Crespo M, Bayón Y, Alonso A.2013.The autoimmunity risk variant LYP-W620 cooperates with CSK in the regulation of TCR signaling. PLoS One 8: e54569. Q1, D1.

Fernandez A, Matias N, Fucho R, Ribas V, Von Montfort C, Nuño N, Baulies A, Martinez L, Tarrats N, Mari M, Colell A, Morales A, Dubuquoy L, Mathurin P, Bataller R, Caballeria J, Elena M, Balsinde J, Kaplowitz N, Garcia-Ruiz C, Fernandez-Checa JC. 2013. ASMase is required for chronic alcohol induced hepatic endoplasmic reticulum stress and mitochondrial cholesterol loading. J Hepatol. 59: 805-813. Q1,D1.

Gil-de-Gómez L, Astudillo AM, Meana C, Rubio JM, Guijas C, Balboa MA, Balsinde J.2013. A phosphatidylinositol species acutely generated by activated macrophages regulates innate immune responses. J. Immunol. 190: 5169-5177. Q1

Francisco V, Costa G, Figueirinha A, Marques C, Pereira P, Neves BM, Lopes MC, García-Rodríguez C, Cruz MT, Batista MT. 2013. Anti-inflammatory activity of Cymbopogon citratus leaves infusion via proteasome and nuclear factor-κB pathway inhibition: contribution of chlorogenic acid. J. Ethnopharmacol. 148: 126-134. Q1.

Vallejo-Diez S, Bernardo D, Moreno Mde L, Muñoz-Suano A, Fernández-Salazar L, Calvo C, Sousa C, Garrote JA, Cebolla A, Arranz E.2013. Detection of specific IgA antibodies against a novel deamidated 8-mer gliadin peptide in blood plasma samples from celiac patients. PLoS One 8 : e80982. Q1,D1.

Arranz E, Peña AS, Bernardo D.2013. Mediators of inflammation and immune responses in the human gastrointestinal tract. Mediators Inflamm. 865638. Q2.

Barrio-Real L, Barrueco M, González-Sarmiento R, Caloca MJ. 2013. Association of a novel polymorphism of the β2-chimaerin gene (CHN2) with smoking. J. Investig. Med. 61: 1129-1131. Q2.

Genética Molecular de la Enfermedad (MGD)

Ruiz M, Sanchez D, Correnti C, Strong RK, Ganfornina MD. 2013. Lipid-binding properties of human ApoD and Lazarillo-related lipocalins: functional implications for cell differentiation. FEBS J. 280: 3928-3943. Q1

Bajo-Grañeras R, Crespo-Sanjuan J, García-Centeno RM, Garrote-Adrados JA, Gutierrez G, García-Tejeiro M, Aguirre-Gervás B, Calvo-Nieves MD, Bustamante R, Ganfornina MD.2013. Sanchez D. Expression and potential role of apolipoprotein D on the death-survival balance of human colorectal cancer cells under oxidative stress conditions. Int. J. Colorectal Dis. 28: 751-766. Q2.

Zuccotti A, Lee SC, Campanelli D, Singer W, Satheesh SV, Patriarchi T, Geisler HS, Köpschall I, Rohbock K, Nothwang HG, Hu J, Hell JW, Schimmang T, Rüttiger L, Knipper M.2013. L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression. Front. Mol. Neurosci. 6: 20. Q3.

Schimmang T, Pirvola U.2013. Coupling the cell cycle to development and regeneration of the inner ear. Semin. Cell Dev. Biol. 24: 507-513. Q1,D1.

Schimmang T.2013. Transcription factors that control inner ear development and their potential for transdifferentiation and reprogramming. Hear. Res. 297: 84-90. Q1.

Singer W, Zuccotti A, Jaumann M, Lee SC, Panford-Walsh R, Xiong H, Zimmermann U, Franz C, Geisler HS, Köpschall I, Rohbock K, Varakina K, Verpoorten S, Reinbothe T, Schimmang T, Rüttiger L, Knipper M.2013. Noise-induced inner hair cell ribbon loss disturbs central arc mobilization: a novel molecular paradigm for understanding tinnitus. Mol. Neurobiol. 47: 261-279. Q1.

Vendrell V, Vázquez-Echeverría C, López-Hernández I, Alonso BD, Martinez S, Pujades C, Schimmang T.2013. Roles of Wnt8a during formation and patterning of the mouse inner ear. Mech. Dev. 130: 160-168. Q3.

Ward Y, Lake R, Martin PL, Killian K, Salerno P, Wang T, Meltzer P, Merino M, Cheng SY, Santoro M, Garcia-Rostan G, Kelly K.2013. CD97 amplifies LPA receptor signaling and promotes thyroid cancer progression in a mouse model. Oncogene 32: 2726-2738. Q1,D1.

Infante M, Durán M, Acedo A, Sánchez-Tapia EM, Díez-Gómez B, Barroso A, García-González M, Feliubadaló L, Lasa A, de la Hoya M, Esteban-Cardeñosa E, Díez O, Martínez-Bouzas C, Godino J, Teulé A, Osorio A, Lastra E, González-Sarmiento R, Miner C, Velasco EA.2013. The highly prevalent BRCA2 mutation c.2808_2811del (3036delACAA) is located in a mutational hotspot and has multiple origins. Carcinogenesis 34: 2505-2511. Q1.

Blanco A, de la Hoya M, Osorio A, Diez O, Miramar MD, Infante M, Martinez-Bouzas C, Torres A, Lasa A, Llort G, Brunet J, Graña B, Perez Segura P, Garcia MJ, Gutiérrez-Enríquez S, Carracedo Á, Tejada MI, Velasco EA, Calvo MT, Balmaña J, Benitez J, Caldés T, Vega A.2013. Analysis of PALB2 gene in BRCA1/BRCA2 negative Spanish hereditary breast/ovarian cancer families with pancreatic cancer cases. PLoS One 8: e67538. Q1,D1.

Pérez-Cabornero L, Infante M, Velasco E, Lastra E, Miner C, Durán M.2013. Genotype-phenotype correlation in MMR mutation-positive families with Lynch syndrome. Int. J. Colorectal Dis. 28: 1195-11201. Q2.

Pérez-Cabornero L, Infante M, Velasco E, Lastra E, Miner C, Durán M.2013. Evaluating the effect of unclassified variants identified in MMR genes using phenotypic features, bioinformatics prediction, and RNA assays. J. Mol. Diagn. 15: 380-390. Q1.

Martínez-Urueña N, Macías L, Pérez-Cabornero L, Infante M, Lastra E, Cruz JJ, Miner C, González R, Durán M.2013. Incidence of -93 MLH1 promoter polymorphism in familial and sporadic colorectal cancer. Colorectal Dis. 15: e118-23. Q2.

Gracia-Aznarez FJ, Fernandez V, Pita G, Peterlongo P, Dominguez O, de la Hoya M, Duran M, Osorio A, Moreno L, Gonzalez-Neira A, Rosa-Rosa JM, Sinilnikova O, Mazoyer S, Hopper J, Lazaro C, Southey M, Odefrey F, Manoukian S, Catucci I, Caldes T, Lynch HT, Hilbers FS, van Asperen CJ, Vasen HF, Goldgar D, Radice P, Devilee P, Benitez J.2013. Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles. PLoS One 8: e55681. Q1,D1.

Osorio A, Bogliolo M, Fernández V, Barroso A, de la Hoya M, Caldés T, Lasa A, Cajal TR, Santamariña M, Vega A, Quiles F, Lázaro C, Díez O, Fernández D, González-Sarmiento R, Durán M, Piqueras JF, Marín M, Pujol R, Surrallés J, Benítez J.2013. Evaluation of rare variants in the new Fanconi anemia gene ERCC4 (FANCQ) as familial breast/ovarian cancer susceptibility alleles. Hum. Mutat. 34: 1615-1618. Q1.

Couch FJ, Wang X, McGuffog L, et al (más de 100 autores).2013. Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. PLoS Genet. 9: e1003212. Q1,D1.

Resumen de la producción