Managing Bardet–Biedl Syndrome—Now and in the Future

Por Forsythe, Elizabeth, Kenny, Joanna, Bacchelli, Chiara, Beales, Philip L.
Publicado no Front Pediatr (2018)

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Por Pocklington, Andrew J., Rees, Elliott, Walters, James T.R., Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter, Moran, Jennifer L., McCarroll, Steven A., Kirov, George, O’Donovan, Michael C., Owen, Michael J.
Publicado no Neuron (2015)

A novel coatomer-related SEA complex dynamically associates with the vacuole in yeast and is implicated in the response to nitrogen starvation

Por Dokudovskaya, Svetlana, Rout, Michael P
Publicado em 2011

Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature

Por Ardissone, Anna, Granata, Tiziana, Legati, Andrea, Diodato, Daria, Melchionda, Laura, Lamantea, Eleonora, Garavaglia, Barbara, Ghezzi, Daniele, Moroni, Isabella
Publicado no JIMD Rep (2015)

The complex legal and ethical issues related to generic medications. Viral hepatitis: a case study

Por Danta, M, Ghinea, N
Publicado no J Virus Erad (2017)

A novel mutation in the succinate dehydrogenase subunit D gene in siblings with the hereditary paraganglioma–pheochromocytoma syndrome

Por Prasad, Chaithra, Oakley, Gerard J, Yip, Linwah, Coyne, Christopher, Rangaswamy, Balasubramanya, Dixit, Sanjay B
Publicado no SAGE Open Med Case Rep (2014)

A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation

Por Dalgaard, Marlene D, Weinhold, Nils, Edsgärd, Daniel, Silver, Jeremy D, Pers, Tune H, Nielsen, John E, Jørgensen, Niels, Juul, Anders, Gerds, Thomas A, Giwercman, Aleksander, Giwercman, Yvonne L, Cohn-Cedermark, Gabriella, Virtanen, Helena E, Toppari, Jorma, Daugaard, Gedske, Jensen, Thomas S, Brunak, Søren, Rajpert-De Meyts, Ewa, Skakkebæk, Niels E, Leffers, Henrik, Gupta, Ramneek
Publicado em 2011

A Case of HDR Syndrome and Ichthyosis: Dual Diagnosis by Whole-Genome Sequencing of Novel Mutations in GATA3 and STS Genes

Por Goodwin, Gregory, Hawley, Pamela P., Miller, David T.
Publicado no J Clin Endocrinol Metab (2016)

A QM-MD simulation approach to the analysis of FRET processes in (bio)molecular systems. A case...

Por Sobieraj, M., Krzyśko, K. A., Jarmuła, A., Kalinowski, M. W., Lesyng, B., Prokopowicz, M., Cieśla, J., Gojdź, A., Kierdaszuk, B.
Publicado no J Mol Model (2015)

Foundations for Streaming Model Transformations by Complex Event Processing

Por Dávid, István, Ráth, István, Varró, Dániel
Publicado no Softw Syst Model (2016)

Conservation of Telomere protein complexes: Shuffling through Evolution

Por Linger, Benjamin R., Price, Carolyn M.
Publicado em 2009

Synthetic Biology: Engineering complexity and refactoring cell capabilities

Por Jean Marie Fran, Pablo Carbonell, Francesca Ceroni, Karmella Ann Haynes
Publicado no Frontiers Research Topics (2015)

Brownie, a Gene Involved in Building Complex Respiratory Devices in Insect Eggshells

Por Irles, Paula, Bellés, Xavier, Piulachs, M. Dolors
Publicado em 2009

Structure of the oligonucleotide d(CGTATATACG) as a site-specific complex with nickel ions.

Por Abrescia, N G, Malinina, L, Fernandez, L G, Huynh-Dinh, T, Neidle, S, Subirana, J A
Publicado em 1999

A novel tensor distribution model for the diffusion-weighted MR signal

Por Jian, Bing, Vemuri, Baba C., Özarslan, Evren, Carney, Paul R., Mareci, Thomas H.
Publicado em 2007

Identification of novel loci affecting entry of Salmonella enteritidis into eukaryotic cells.

Por Stone, B J, Garcia, C M, Badger, J L, Hassett, T, Smith, R I, Miller, V L
Publicado em 1992

Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

Por Jackson, Robert S., Creemers, John W.M., Farooqi, I. Sadaf, Raffin-Sanson, Marie-Laure, Varro, Andrea, Dockray, Graham J., Holst, Jens J., Brubaker, Patricia L., Corvol, Pierre, Polonsky, Kenneth S., Ostrega, Diane, Becker, Kenneth L., Bertagna, Xavier, Hutton, John C., White, Anne, Dattani, Mehul T., Hussain, Khalid, Middleton, Stephen J., Nicole, Thomasina M., Milla, Peter J., Lindley, Keith J., O’Rahilly, Stephen
Publicado em 2003

Microbiology, Genomics, and Clinical Significance of the Pseudomonas fluorescens Species Complex, an Unappreciated Colonizer of Humans

Por Scales, Brittan S., Dickson, Robert P., LiPuma, John J., Huffnagle, Gary B.
Publicado em 2014

Faster Synthesis of Beta-Diketonate Ternary Europium Complexes: Elapsed Times & Reaction Yields

Por Lima, Nathalia B. D., Silva, Anderson I. S., Gerson, P. C., Gonçalves, Simone M. C., Simas, Alfredo M.
Publicado no PLoS One (2015)

Novel exon 12 mutations in the HIF2A gene associated with erythrocytosis

Por Percy, Melanie J., Beer, Philip A., Campbell, Gavin, Dekker, Ad W., Green, Anthony R., Oscier, David, Rainey, M. Glenn, van Wijk, Richard, Wood, Marion, Lappin, Terence R. J., McMullin, Mary Frances, Lee, Frank S.
Publicado em 2008