Peroxisomal d-hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Por van Grunsven, Elisabeth G., van Berkel, Emanuel, Ijlst, Lodewijk, Vreken, Peter, de Klerk, Johannis B. C., Adamski, Jerzy, Lemonde, Hugh, Clayton, Peter T., Cuebas, Dean A., Wanders, Ronald J. A.
Publicado em 1998

Electrostatic confinement and manipulation of DNA molecules for genome analysis

Por Kounovsky-Shafer, Kristy L., Hernandez-Ortiz, Juan P., Potamousis, Konstantinos, Tsvid, Gene, Place, Michael, Ravindran, Prabu, Jo, Kyubong, Zhou, Shiguo, Odijk, Theo, de Pablo, Juan J., Schwartz, David C.
Publicado no Proc Natl Acad Sci U S A (2017)

Structure-Function Relationships of the Raloxifene-Estrogen Receptor-α Complex for Regulating Transforming Growth Factor-α Expression in Breast Cancer Cells

Por Liu, Hong, Park, Woo-Chan, Bentrem, David J., McKian, Kevin P., Reyes, Alexander De Los, Loweth, Jessica A., Schafer, Jennifer MacGregor, Zapf, James W., Jordan, V. Craig
Publicado em 2001

Ancient Transposable Elements Transformed the Uterine Regulatory Landscape and Transcriptome during the Evolution of Mammalian Pregnancy

Por Lynch, Vincent J., Nnamani, Mauris C., Kapusta, Aurélie, Brayer, Kathryn, Plaza, Silvia L., Mazur, Erik C., Emera, Deena, Sheikh, Shehzad Z., Grützner, Frank, Bauersachs, Stefan, Graf, Alexander, Young, Steven L., Lieb, Jason D., DeMayo, Francesco J., Feschotte, Cédric, Wagner, Günter P.
Publicado no Cell Rep (2015)

Current topics in complement

Por Lambris, J. D.
Publicado em 2006

Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism

Por Cenacchi, G, Fanin, M, De Giorgi, L B, Angelini, C
Publicado em 2005

Glutathione and the redox control system trypanothione/trypanothione reductase are involved...

Por P.R.T. Romão, J. Tovar, S.G. Fonseca, R.H. Moraes, A.K. Cruz, J.S. Hothersall, A.A. Noronha-Dutra, S.H. Ferreira, F.Q. Cunha
Publicado em 2006-03-01

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

Por Rioux, John D., Goyette, Philippe, Vyse, Timothy J., Hammarström, Lennart, Fernando, Michelle M. A., Green, Todd, De Jager, Philip L., Foisy, Sylvain, Wang, Joanne, de Bakker, Paul I. W., Leslie, Stephen, McVean, Gilean, Padyukov, Leonid, Alfredsson, Lars, Annese, Vito, Hafler, David A., Pan-Hammarström, Qiang, Matell, Ritva, Sawcer, Stephen J., Compston, Alastair D., Cree, Bruce A. C., Mirel, Daniel B., Daly, Mark J., Behrens, Tim W., Klareskog, Lars, Gregersen, Peter K., Oksenberg, Jorge R., Hauser, Stephen L.
Publicado em 2009

Breast cancer and molecular medicine

Por Piccart, Martine J.
Publicado em 2006

An integrated tool for determining the primary origin site of metastatic tumours

Por dos Santos, Marcos Tadeu, de Souza, Bruno Feres, Cárcano, Flavio Mavignier, Vidal, Ramon de Oliveira, Scapulatempo-Neto, Cristovam, Viana, Cristiano Ribeiro, Carvalho, Andre Lopes
Publicado no J Clin Pathol (2018)

Brain-Derived Neurotrophic Factor Controls Cannabinoid CB(1) Receptor Function in the Striatum

Por De Chiara, Valentina, Angelucci, Francesco, Rossi, Silvia, Musella, Alessandra, Cavasinni, Francesca, Cantarella, Cristina, Mataluni, Giorgia, Sacchetti, Lucia, Napolitano, Francesco, Castelli, Maura, Caltagirone, Carlo, Bernardi, Giorgio, Maccarrone, Mauro, Usiello, Alessandro, Centonze, Diego
Publicado no J Neurosci (2010)

A systems biology approach to defining regulatory mechanisms for cartilage and tendon cell phenotypes

Por Mueller, A. J., Tew, S. R., Vasieva, O., Clegg, P. D., Canty-Laird, E. G.
Publicado no Sci Rep (2016)

Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans

Por Abe, Koichiro, Cox, Allison, Takamatsu, Nobuhiko, Velez, Gabriel, Laxer, Ronald M., Tse, Shirley M. L., Mahajan, Vinit B., Bassuk, Alexander G., Fuchs, Helmut, Ferguson, Polly J., Hrabe de Angelis, Martin
Publicado no Proc Natl Acad Sci U S A (2019)

Partial trisomy 6p: 46,XX, -10, der(10),t(6;10) (p22;q26)pat and HLA localisation.

Por Ferrando, P, San Román, C, Rodriguez de Cordoba, S, Arnaiz-Villena, A
Publicado em 1981

Multiple gene movements into and out of haploid sex chromosomes

Por Agnieszka P. Lipinska, Nicholas R. T. Toda, Svenja Heesch, Akira F. Peters, J. Mark Cock, Susana M. Coelho
Publicado em 2017-06-01

Cannabidiol: A Promising Drug for Neurodegenerative Disorders?

Por Iuvone, Teresa, Esposito, Giuseppe, De Filippis, Daniele, Scuderi, Caterina, Steardo, Luca
Publicado no CNS Neurosci Ther (2009)

Mapping genetic influences on ventricular structure in twins

Por Chou, Yi-Yu, Leporé, Natasha, Chiang, Ming-Chang, Avedissian, Christina, Barysheva, Marina, McMahon, Katie L., de Zubicaray, Greig I., Meredith, Matthew, Wright, Margaret J., Toga, Arthur W., Thompson, Paul M.
Publicado em 2008

OR02-4 YAP1 Overexpression Associates With Worse Prognosis In Patients With Adrenal Tumors And YAP1 Inhibition By Verteporfin Reduces Tumorigenicity And Reverses Epithelial-mesench...

Por Bellido More, Candy, Bueno, Ana, De Castro, Margaret, Rauber Antonini, Sonir
Publicado no J Endocr Soc (2019)

Cytokine mRNA induction by Interleukin-1β or Tumor Necrosis Factor α in vitro and in vivo

Por Taishi, Ping, Churchill, Lynn, De, Alok, Obal, Ferenc, Krueger, James M.
Publicado em 2008

Residues K465 and G467 within the Cytoplasmic Domain of GP2 Play a Critical Role in the Persistence of Lymphocytic Choriomeningitis Virus in Mice

Por Iwasaki, Masaharu, Ng, Cherie T., Cubitt, Beatrice, de la Torre, Juan C.
Publicado no J Virol (2016)