Zobrazeno 1 - 10
of 281
pro vyhledávání: '"John D. Murdoch"'
Autor:
Katja Burk, John D. Murdoch, Siona Freytag, Melanie Koenig, Vinita Bharat, Ronja Markworth, Susanne Burkhardt, Andre Fischer, Camin Dean
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-19 (2017)
Abstract The sorting of activated receptors into distinct endosomal compartments is essential to activate specific signaling cascades and cellular events including growth and survival. However, the proteins involved in this sorting are not well under
Externí odkaz:
https://doaj.org/article/5db9c009a4ee437b86f567fcdc973904
Autor:
John D. Murdoch, Christine M. Rostosky, Sindhuja Gowrisankaran, Amandeep S. Arora, Sandra-Fausia Soukup, Ramon Vidal, Vincenzo Capece, Siona Freytag, Andre Fischer, Patrik Verstreken, Stefan Bonn, Nuno Raimundo, Ira Milosevic
Publikováno v:
Cell Reports, Vol 17, Iss 4, Pp 1071-1086 (2016)
Endophilin-A, a well-characterized endocytic adaptor essential for synaptic vesicle recycling, has recently been linked to neurodegeneration. We report here that endophilin-A deficiency results in impaired movement, age-dependent ataxia, and neurodeg
Externí odkaz:
https://doaj.org/article/b3675368bb464b4481786ffb5883f006
Autor:
John D Murdoch, Abha R Gupta, Stephan J Sanders, Michael F Walker, John Keaney, Thomas V Fernandez, Michael T Murtha, Samuel Anyanwu, Gordon T Ober, Melanie J Raubeson, Nicholas M DiLullo, Natalie Villa, Zainabdul Waqar, Catherine Sullivan, Luis Gonzalez, A Jeremy Willsey, So-Yeon Choe, Benjamin M Neale, Mark J Daly, Matthew W State
Publikováno v:
PLoS Genetics, Vol 11, Iss 1, p e1004852 (2015)
Contactins and Contactin-Associated Proteins, and Contactin-Associated Protein-Like 2 (CNTNAP2) in particular, have been widely cited as autism risk genes based on findings from homozygosity mapping, molecular cytogenetics, copy number variation anal
Externí odkaz:
https://doaj.org/article/032f22b95c454267af5fad02cfa2ee09
Autor:
Paul Mitchell, Alexander Dobrovic, John D Murdoch, Hongdo Do, Ramyar Molania, Rita Vaiskunaite
Publikováno v:
Clinical Chemistry. 63:1506-1514
BACKGROUNDFalse-positive EGFR T790M mutations have been reported in formalin-fixed lung tumors, but the cause of the false positives has not been identified. The T790M mutation results from a C>T change at the cytosine of a CpG dinucleotide. The pres
Autor:
John D. Murdoch, Siona Freytag, Katja Burk, Ronja Markworth, Camin Dean, Melanie Koenig, Susanne Burkhardt, Andre Fischer, Vinita Bharat
Publikováno v:
Scientific reports 7(1), 2149 (2017). doi:10.1038/s41598-017-02202-4
Scientific Reports, Vol 7, Iss 1, Pp 1-19 (2017)
Scientific Reports
Scientific Reports, Vol 7, Iss 1, Pp 1-19 (2017)
Scientific Reports
The sorting of activated receptors into distinct endosomal compartments is essential to activate specific signaling cascades and cellular events including growth and survival. However, the proteins involved in this sorting are not well understood. We
Autor:
Hongdo, Do, Ramyar, Molania, Paul L, Mitchell, Rita, Vaiskunaite, John D, Murdoch, Alexander, Dobrovic
Publikováno v:
Clinical chemistry. 63(9)
False-positiveFormalin-fixed normal lung tissues and lung squamous cell carcinomas were tested to measure the frequency of false-positiveArtifactualBoth U:G and T:G lesions in formalin-fixed tissue are sources of false-positive