A potential wound-healing-promoting peptide from salamander skin

Por Mu, Lixian, Tang, Jing, Liu, Han, Shen, Chuanbin, Rong, Mingqiang, Zhang, Zhiye, Lai, Ren
Publicado no FASEB J (2014)

A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease

Por Korpaisarn, Sira, Trachoo, Objoon, Panthan, Bhakbhoom, Aroonroch, Rangsima, Suvikapakornkul, Ronnarat, Sriphrapradang, Chutintorn
Publicado no Case Rep Oncol (2017)

Telescopic Corsair in 5F Guidion for Retrograde Recanalization of Complex Chronic Total Occlusions (CTOs)

Por Palmers, Pieter-Jan, Maeremans, Joren, Meyer-Gessner, Markus, Bataille, Yoann, Dens, Joseph
Publicado no Am J Case Rep (2017)

A novel PRKAR1A mutation resulting in a splicing variant in a case of Carney complex

Por Jang, Yi Sun, Moon, Sung Dae, Kim, Ju Hee, Lee, Ihn Suk, Lee, Jong Min, Kim, Hye Soo
Publicado no Korean J Intern Med (2015)

Computational modeling of bone fracture non-unions: four clinically relevant case studies

Por Carlier, Aurélie, Lammens, Johan, Van Oosterwyck, Hans, Geris, Liesbet
Publicado no In Silico Cell Tissue Sci (2015)

Proliferative, necrotizing and crescentic immune complex-mediated glomerulonephritis in a cat

Por Gross, Carolyn, Cianciolo, Rachel E, Lees, George E, Brown, Cathy A, Foster, Jonathan D
Publicado no JFMS Open Rep (2015)

Reliable Determination of Site-specific in vivo Protein N-Glycosylation based on Collision-Induced MS/MS and Chromatographic Retention Time

Por Wang, Benlian, Tsybovsky, Yaroslav, Palczewski, Krzysztof, Chance, Mark R.
Publicado em 2014

Mycobacterium heraklionense sp. nov.: A case series

Por NEONAKIS, IOANNIS K., SPANDIDOS, DEMETRIOS A., GITTI, ZOE
Publicado no Exp Ther Med (2015)

Dbf4‐dependent kinase and the Rtt107 scaffold promote Mus81‐Mms4 resolvase activation during mitosis

Por Princz, Lissa N, Wild, Philipp, Bittmann, Julia, Aguado, F Javier, Blanco, Miguel G, Matos, Joao, Pfander, Boris
Publicado no EMBO J (2017)

Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus

Por Moldován, Norbert, Tombácz, Dóra, Szűcs, Attila, Csabai, Zsolt, Balázs, Zsolt, Kis, Emese, Molnár, Judit, Boldogkői, Zsolt
Publicado no Sci Rep (2018)

Early onset of Chanarin-Dorfman syndrome with severe liver involvement in a patient with a complex rearrangement of ABHD5 promoter

Por Missaglia, Sara, Valadares, Eugenia Ribeiro, Moro, Laura, Faguntes, Eleonora Druve Tavares, quintão Roque, Raquel, Giardina, Bruno, Tavian, Daniela
Publicado em 2014

Severe bleeding complications and multiple kidney transplants in a patient with tuberous sclerosis complex caused by a novel TSC2 missense variant

Por Živčić-Ćosić, Stela, Mayer, Karin, Đorđević, Gordana, Nellist, Mark, Hoogeveen-Westerveld, Marianne, Miletić, Damir, Rački, Sanjin, Klein, Hanns-Georg, Trobonjača, Zlatko
Publicado no Croat Med J (2017)

Novel remote electronic medication supply model for opioid-dependent outpatients with polypharmacy––first long-term case study

Por Allemann, Samuel S., Dürsteler, Kenneth M., Strasser, Johannes, Vogel, Marc, Stoeckle, Marcel, Hersberger, Kurt E., Arnet, Isabelle
Publicado no Harm Reduct J (2017)

External influences and priority-setting for anti-cancer agents: a case study of media coverage in adjuvant trastuzumab for breast cancer

Por Booth, Christopher M, Dranitsaris, George, Gainford, M Corona, Berry, Scott, Fralick, Michael, Fralick, John, Sue, Joanna, Clemons, Mark
Publicado em 2007

Engineering proximal vs. distal heme–NO coordination via dinitrosyl dynamics: implications for NO sensor design

Por Kekilli, Demet, Petersen, Christine A., Pixton, David A., Ghafoor, Dlzar D., Abdullah, Gaylany H., Dworkowski, Florian S. N., Wilson, Michael T., Heyes, Derren J., Hardman, Samantha J. O., Murphy, Loretta M., Strange, Richard W., Scrutton, Nigel S., Andrew, Colin R., Hough, Michael A.
Publicado no Chem Sci (2017)

Anti-IgLON5 Disease: A Case With 11-Year Clinical Course and Review of the Literature

Por Mette Scheller Nissen, Mette Scheller Nissen, Mette Scheller Nissen, Morten Blaabjerg, Morten Blaabjerg, Morten Blaabjerg
Publicado em 2019-10-01

Rfc5p regulates alternate RFC complex functions in sister chromatid pairing reactions in budding yeast

Por Maradeo, Marie E, Garg, Anisha, Skibbens, Robert V
Publicado em 2010

Lethal neonatal mitochondrial phenotype caused by a novel polymerase subunit gamma mutation: A case report

Por AlJabri, Mohamed F., Kamal, Naglaa M., Halabi, Abdulrahman, Korbi, Haifa, Alsayyali, Mashhour M.A., Alzahrani, Yahea A.
Publicado no Medicine (Baltimore) (2018)

Development of a meta-algorithm for guiding primary care encounters for patients...

Por Muche-Borowski, Cathleen, Lühmann, Dagmar, Schäfer, Ingmar, Mundt, Rebekka, Wagner, Hans-Otto, Scherer, Martin
Publicado no BMJ Open (2017)

Intractable epileptic spasms in a patient with Pontocerebellar hypoplasia: Severe phenotype of type 2 or another subtype?

Por Samanta, Debopam, Willis, Erin
Publicado no Ann Indian Acad Neurol (2016)