Increased osteoclastogenesis contributes to bone loss in the Costello syndrome Hras G12V mouse model.
Frontiers In Cell And Developmental Biology
Nandi, Sayantan S; Chennappan, Saravanakkumar S; Andrasch, Yannik Y; Fidan, Miray M; Engler, Melanie M; Ahmad, Mubashir M; Tuckermann, Jan P JP; Zenker, Martin M; Cirstea, Ion Cristian IC
A Phase I-II multicenter trial with Avelumab plus autologous dendritic cell vaccine in pre-treated mismatch repair-proficient (MSS) metastatic colorectal cancer patients; GEMCAD 1602 study.
Cancer Immunology, Immunotherapy : Cii
Español-Rego, Marta M; Fernández-Martos, Carlos C; Elez, Elena E; Foguet, Carles C; Pedrosa, Leire L; Rodríguez, Nuria N; Ruiz-Casado, Ana A; Pineda, Estela E; Cid, Joan J; Cabezón, Raquel R; Oliveres, Helena H; Lozano, Miquel M; Ginés, Angels A; García-Criado, Angeles A; Ayuso, Juan Ramon JR; Pagés, Mario M; Cuatrecasas, Miriam M; Torres, Ferràn F; Thomson, Timothy T; Cascante, Marta M; Benítez-Ribas, Daniel D; Maurel, Joan J
Deletion of Lactate Dehydrogenase-A Impairs Oncogene-Induced Mouse Hepatocellular Carcinoma Development.
Cellular And Molecular Gastroenterology And Hepatology
Serra, Marina M; Di Matteo, Mario M; Serneels, Jens J; Pal, Rajesh R; Cafarello, Sarah Trusso ST; Lanza, Martina M; Sanchez-Martin, Carlos C; Evert, Matthias M; Castegna, Alessandra A; Calvisi, Diego Francesco DF; Mazzone, Massimiliano M; Columbano, Amedeo A
Indirect cholinergic activation slows down pancreatic cancer growth and tumor-associated inflammation.
Journal Of Experimental & Clinical Cancer Research : Cr
Pfitzinger, Paulo L PL; Fangmann, Laura L; Wang, Kun K; Demir, Elke E; Gürlevik, Engin E; Fleischmann-Mundt, Bettina B; Brooks, Jennifer J; D'Haese, Jan G JG; Teller, Steffen S; Hecker, Andreas A; Jesinghaus, Moritz M; Jäger, Carsten C; Ren, Lei L; Istvanffy, Rouzanna R; Kühnel, Florian F; Friess, Helmut H; Ceyhan, Güralp Onur GO; Demir, Ihsan Ekin IE
SHP2 mutations induce precocious gliogenesis of Noonan syndrome-derived iPSCs during neural development in vitro.
Stem Cell Research & Therapy
Ju, Younghee Y; Park, Jun Sung JS; Kim, Daejeong D; Kim, Bumsoo B; Lee, Jeong Ho JH; Nam, Yoonkey Y; Yoo, Han-Wook HW; Lee, Beom Hee BH; Han, Yong-Mahn YM
Costello syndrome: Clinical phenotype, genotype, and management guidelines.
American Journal Of Medical Genetics. Part A
Gripp, Karen W KW; Morse, Lindsey A LA; Axelrad, Marni M; Chatfield, Kathryn C KC; Chidekel, Aaron A; Dobyns, William W; Doyle, Daniel D; Kerr, Bronwyn B; Lin, Angela E AE; Schwartz, David D DD; Sibbles, Barbara J BJ; Siegel, Dawn D; Shankar, Suma P SP; Stevenson, David A DA; Thacker, Mihir M MM; Weaver, K Nicole KN; White, Sue M SM; Rauen, Katherine A KA
Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp.
American Journal Of Medical Genetics. Part A
Bertola, Débora D; Buscarilli, Michelle M; Stabley, Deborah L DL; Baker, Laura L; Doyle, Daniel D; Bartholomew, Dennis W DW; Sol-Church, Katia K; Gripp, Karen W KW
Respiratory system involvement in Costello syndrome.
American Journal Of Medical Genetics. Part A
Gomez-Ospina, Natalia N; Kuo, Christin C; Ananth, Amitha Lakshmi AL; Myers, Angela A; Brennan, Marie-Luise ML; Stevenson, David A DA; Bernstein, Jonathan A JA; Hudgins, Louanne L
Dendritic cells pulsed with tumor cells killed by high hydrostatic pressure induce strong immune responses and display therapeutic effects both in murine TC-1 and TRAMP-C2 tumors when combined with docetaxel chemotherapy.
International Journal Of Oncology
Mikyšková, Romana R; Štěpánek, Ivan I; Indrová, Marie M; Bieblová, Jana J; Šímová, Jana J; Truxová, Iva I; Moserová, Irena I; Fučíková, Jitka J; Bartůňková, Jiřina J; Špíšek, Radek R; Reiniš, Milan M
In vivo synaptic transmission and morphology in mouse models of Tuberous sclerosis, Fragile X syndrome, Neurofibromatosis type 1, and Costello syndrome.
Frontiers In Cellular Neuroscience
Wang, Tiantian T; de Kok, Laura L; Willemsen, Rob R; Elgersma, Ype Y; Borst, J Gerard G JG
The role of p19 and p21 H-Ras proteins and mutants in miRNA expression in cancer and a Costello syndrome cell model.
Bmc Medical Genetics
García-Cruz, Roseli R; Camats, Maria M; Calin, George A GA; Liu, Chang-Gong CG; Volinia, Stefano S; Taccioli, Cristian C; Croce, Carlo M CM; Bach-Elias, Montse M
Dissecting Genomic Aberrations in Myeloproliferative Neoplasms by Multiplex-PCR and Next Generation Sequencing.
Plos One
Kirschner, Martin M J MM; Schemionek, Mirle M; Schubert, Claudia C; Chatain, Nicolas N; Sontag, Stephanie S; Isfort, Susanne S; Ortiz-Brüchle, Nadina N; Schmitt, Karla K; Krüger, Luisa L; Zerres, Klaus K; Zenke, Martin M; Brümmendorf, Tim H TH; Koschmieder, Steffen S
miRNA-130b is required for the ERK/FOXM1 pathway activation-mediated protective effects of isosorbide dinitrate against mesenchymal stem cell senescence induced by high glucose.
Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Giannoulatou, Eleni E; McVean, Gilean G; Taylor, Indira B IB; McGowan, Simon J SJ; Maher, Geoffrey J GJ; Iqbal, Zamin Z; Pfeifer, Susanne P SP; Turner, Isaac I; Burkitt Wright, Emma M M EM; Shorto, Jennifer J; Itani, Aysha A; Turner, Karen K; Gregory, Lorna L; Buck, David D; Rajpert-De Meyts, Ewa E; Looijenga, Leendert H J LH; Kerr, Bronwyn B; Wilkie, Andrew O M AO; Goriely, Anne A
Goodwin, Alice F AF; Tidyman, William E WE; Jheon, Andrew H AH; Sharir, Amnon A; Zheng, Xu X; Charles, Cyril C; Fagin, James A JA; McMahon, Martin M; Diekwisch, Thomas G H TG; Ganss, Bernhard B; Rauen, Katherine A KA; Klein, Ophir D OD
RIP1 potentiates BPDE-induced transformation in human bronchial epithelial cells through catalase-mediated suppression of excessive reactive oxygen species.
A SUMOylation Motif in Aurora-A: Implications for Spindle Dynamics and Oncogenesis.
Frontiers In Oncology
Pérez de Castro, Ignacio I; Aguirre-Portolés, Cristina C; Martin, Benedicte B; Fernández-Miranda, Gonzalo G; Klotzbucher, Andrea A; Kubbutat, Michael H G MH; Megías, Diego D; Arlot-Bonnemains, Yannick Y; Malumbres, Marcos M
MEK-ERK pathway modulation ameliorates disease phenotypes in a mouse model of Noonan syndrome associated with the Raf1(L613V) mutation.
The Journal Of Clinical Investigation
Wu, Xue X; Simpson, Jeremy J; Hong, Jenny H JH; Kim, Kyoung-Han KH; Thavarajah, Nirusha K NK; Backx, Peter H PH; Neel, Benjamin G BG; Araki, Toshiyuki T
Enhanced human brain associative plasticity in Costello syndrome.
The Journal Of Physiology
Dileone, M M; Profice, P P; Pilato, F F; Alfieri, P P; Cesarini, L L; Mercuri, E E; Leoni, C C; Tartaglia, M M; Di Iorio, R R; Zampino, G G; Di Lazzaro, V V
Common activation of canonical Wnt signaling in pancreatic adenocarcinoma.
Plos One
Pasca di Magliano, Marina M; Biankin, Andrew V AV; Heiser, Patrick W PW; Cano, David A DA; Gutierrez, Pedro J A PJ; Deramaudt, Therese T; Segara, Davendra D; Dawson, Amanda C AC; Kench, James G JG; Henshall, Susan M SM; Sutherland, Robert L RL; Dlugosz, Andrzej A; Rustgi, Anil K AK; Hebrok, Matthias M
Myopathy caused by HRAS germline mutations: implications for disturbed myogenic differentiation in the presence of constitutive HRas activation.
Journal Of Medical Genetics
van der Burgt, Ineke I; Kupsky, William W; Stassou, Stephani S; Nadroo, Ali A; Barroso, Cândida C; Diem, Angelika A; Kratz, Christian P CP; Dvorsky, Radovan R; Ahmadian, Mohammad Reza MR; Zenker, Martin M