A Novel Cardioport for Beating-Heart Image-Guided Intracardiac Surgery

Por Vasilyev, Nikolay V., Kawata, Mitsuhiro, DiBiasio, Christopher M., Durand, Keith V., Hopkins, Jonathan, Traina, Zachary J., Slocum, Alexander H., del Nido, Pedro J.
Publicado em 2011

Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene

Por Çim, Abdullah, Coşkun, Salih, Görükmez, Orhan, Yüksel, Hatice, Uluca, Ünal, Di Pietro, Erminia, Plourde, François, Elise Braverman, Nancy
Publicado no J Clin Res Pediatr Endocrinol (2015)

STAT3-mediated Coincidence Detection Regulates Noncanonical Immediate Early Gene Induction

Por Waitkus, Matthew S., Chandrasekharan, Unni M., Willard, Belinda, Haque, S. Jaharul, DiCorleto, Paul E.
Publicado em 2013

Human Myo19 is a novel myosin that associates with mitochondria

Por Quintero, Omar A., DiVito, Melinda M., Adikes, Rebecca C., Kortan, Melisa B., Case, Lindsay B., Lier, Audun J., Panaretos, Niki S., Slater, Stephanie Q., Rengarajan, Michelle, Feliu, Marianela, Cheney, Richard E.
Publicado em 2009

Detection of ALK translocation in non-small cell lung carcinoma (NSCLC) and its clinicopathological...

Por Yang, Lin, Ling, Yun, Guo, Lei, Ma, Di, Xue, Xuemin, Wang, Bingning, Li, Junling, Ying, Jianming
Publicado no Chin J Cancer Res (2016)

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

Por Sutherland, H. F., Wadey, R., McKie, J. M., Taylor, C., Atif, U., Johnstone, K. A., Halford, S., Kim, U. J., Goodship, J., Baldini, A., Scambler, P. J.
Publicado em 1996

Longitudinal Follow-up of Chronic Pulmonary Manifestations in Esophageal Atresia: A Clinical Algorithm and Review of the Literature

Por Virginia Mirra, Marco Maglione, Laida L. Di Micco, Silvia Montella, Francesca Santamaria
Publicado em 2017-02-01

Recurrent Myoglobinuria in a Sporadic Patient with a Novel Mitochondrial DNA tRNA(Ile) Mutation

Por Emmanuele, Valentina, Sotiriou, Evangelia, Shirazi, Maryam, Tanji, Kurenai, Haller, Ronald G., Heinicke, Katja, Bosch, Peter E., Hirano, Michio, DiMauro, Salvatore
Publicado em 2011

The BioDICE Taverna plugin for clustering and visualization of biological data: a workflow for molecular compounds exploration

Por Fiannaca, Antonino, Rosa, Massimo La, Fatta, Giuseppe Di, Gaglio, Salvatore, Rizzo, Riccardo, Urso, Alfonso
Publicado em 2014

Gαs regulates Glucagon-Like Peptide 1 Receptor-mediated cyclic AMP generation at Rab5 endosomal compartment

Por Girada, Shravan Babu, Kuna, Ramya S., Bele, Shilpak, Zhu, Zhimeng, Chakravarthi, N.R., DiMarchi, Richard D., Mitra, Prasenjit
Publicado no Mol Metab (2017)

The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism

Por Pesce, Emanuela, Sondo, Elvira, Ferrera, Loretta, Tomati, Valeria, Caci, Emanuela, Scudieri, Paolo, Musante, Ilaria, Renda, Mario, Baatallah, Nesrine, Servel, Nathalie, Hinzpeter, Alexandre, di Bernardo, Diego, Pedemonte, Nicoletta, Galietta, Luis J. V.
Publicado no Front Pharmacol (2018)

A multiple myeloma-specific capture sequencing platform discovers novel translocations and frequent, risk-associated point mutations in IGLL5

Por White, Brian S., Lanc, Irena, O’Neal, Julie, Gupta, Harshath, Fulton, Robert S., Schmidt, Heather, Fronick, Catrina, Belter, Edward A., Fiala, Mark, King, Justin, Ahmann, Greg J., DeRome, Mary, Mardis, Elaine R., Vij, Ravi, DiPersio, John F., Levy, Joan, Auclair, Daniel, Tomasson, Michael H.
Publicado no Blood Cancer J (2018)

The Contribution of the Video Capsule Endoscopy in Establishing the Indication of Surgical Treatment in the Tumoral Pathology of the Small Bowel

Por Vere, C.C., Streba, C.T., Rogoveanu, I., Georgescu, M., Pirvu, D., Iordache, Sevastita, Gheonea, D.I., Saftoiu, A., Ciurea, T.
Publicado em 2012

Acute graft-versus-host disease following lung transplantation in a patient with a novel TERT mutation

Por Brestoff, Jonathan R, Vessoni, Alexandre T, Brenner, Kirsten A, Uy, Geoffrey L, DiPersio, John F, Blinder, Morey, Witt, Chad A, Byers, Derek E, Hachem, Ramsey R, Truclock, Elbert P, Early, Dayna S, Anadkat, Milan J, Musiek, Amy, Javidan-Nejad, Cylen, Balfe, Dennis M, Rosman, Ilana S, Liu, Chang, Zhang, Lingxin, Despotis, George J, Ruzinova, Marianna B, Sehn, Jennifer K, Amarillo, Ina, Heusel, Jonathan W, Swat, Wojcieh, Kim, Brian S, Wartman, Lukas D, Yusen, Roger D, Batista, Luis F Z
Publicado no Thorax (2018)

Real-time diagnosis of H. pylori infection during endoscopy: Accuracy of an innovative tool (EndoFaster)

Por Costamagna, Guido, Zullo, Angelo, Bizzotto, Alessandra, Spada, Cristiano, Hassan, Cesare, Riccioni, Maria Elena, Marmo, Clelia, Strangio, Giuseppe, Di Rienzo, Teresa Antonella, Cammarota, Giovanni, Gasbarrini, Antonio, Repici, Alessandro
Publicado no United European Gastroenterol J (2015)

Opioid Drug-Drug-Drug Interactions and Unintentional Traumatic Injury: Screening to Detect Three-Way Drug Interaction Signals

Por Emily K. Acton, Emily K. Acton, Emily K. Acton, Sean Hennessy, Sean Hennessy, Sean Hennessy, Sean Hennessy, Colleen M. Brensinger, Colleen M. Brensinger, Warren B. Bilker, Warren B. Bilker, Warren B. Bilker, Todd A. Miano, Todd A. Miano, Sascha Dublin, Sascha Dublin, John R. Horn, Sophie Chung, Douglas J. Wiebe, Douglas J. Wiebe, Douglas J. Wiebe, Allison W. Willis, Allison W. Willis, Allison W. Willis, Allison W. Willis, Charles E. Leonard, Charles E. Leonard, Charles E. Leonard
Publicado em 2022-05-01

Whole Exome Sequencing Uncovers Germline Variants of Cancer-Related Genes in Sporadic Pheochromocytoma

Por Urbini, Milena, Nannini, Margherita, Astolfi, Annalisa, Indio, Valentina, Vicennati, Valentina, De Luca, Matilde, Tarantino, Giuseppe, Corso, Federica, Saponara, Maristella, Gatto, Lidia, Santini, Donatella, Di Dalmazi, Guido, Pagotto, Uberto, Pasquali, Renato, Pession, Andrea, Biasco, Guido, Pantaleo, Maria A.
Publicado no Int J Genomics (2018)

Emergence and Adaptation of a Novel Highly Pathogenic H7N9 Influenza Virus in Birds and Humans from a 2013 Human-Infecting Low-Pathogenic Ancestor

Por Qi, Wenbao, Jia, Weixin, Liu, Di, Li, Jing, Bi, Yuhai, Xie, Shumin, Li, Bo, Hu, Tao, Du, Yingying, Xing, Li, Zhang, Jiahao, Zhang, Fuchun, Wei, Xiaoman, Eden, John-Sebastian, Li, Huanan, Tian, Huaiyu, Li, Wei, Su, Guanming, Lao, Guangjie, Xu, Chenggang, Xu, Bing, Liu, Wenjun, Zhang, Guihong, Ren, Tao, Holmes, Edward C., Cui, Jie, Shi, Weifeng, Gao, George F., Liao, Ming
Publicado no J Virol (2018)

Association Between Mutation Clearance After Induction Therapy and Outcomes in Acute Myeloid Leukemia

Por Klco, Jeffery M., Miller, Christopher A., Griffith, Malachi, Petti, Allegra, Spencer, David H., Ketkar-Kulkarni, Shamika, Wartman, Lukas D, Christopher, Matthew, Lamprecht, Tamara L., Helton, Nicole M., Duncavage, Eric J., Payton, Jacqueline E., Baty, Jack, Heath, Sharon E., Griffith, Obi L., Shen, Dong, Hundal, Jasreet, Chang, Gue Su, Fulton, Robert, O'Laughlin, Michelle, Fronick, Catrina, Magrini, Vincent, Demeter, Ryan T., Larson, David E., Kulkarni, Shashikant, Ozenberger, Bradley A., Welch, John S, Walter, Matthew J, Graubert, Timothy A., Westervelt, Peter, Radich, Jerald P., Link, Daniel C., Mardis, Elaine R., DiPersio, John F., Wilson, Richard K., Ley, Timothy J.
Publicado no JAMA (2015)

Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

Por Nasca, Alessia, Rizza, Teresa, Doimo, Mara, Legati, Andrea, Ciolfi, Andrea, Diodato, Daria, Calderan, Cristina, Carrara, Gianfranco, Lamantea, Eleonora, Aiello, Chiara, Di Nottia, Michela, Niceta, Marcello, Lamperti, Costanza, Ardissone, Anna, Bianchi-Marzoli, Stefania, Iarossi, Giancarlo, Bertini, Enrico, Moroni, Isabella, Tartaglia, Marco, Salviati, Leonardo, Carrozzo, Rosalba, Ghezzi, Daniele
Publicado no Orphanet J Rare Dis (2017)