PMC Links for Nucleotide (Select 1519311732) - PMC

Select item 64366221.

Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations

Ratna Tripathy, Ines Leca, Tessa van Dijk, Janneke Weiss, Bregje W van Bon, Maria Christina Sergaki, Thomas Gstrein, Martin Breuss, Guoling Tian, Nadia Bahi-Buisson, Alexander R. Paciorkowski, Alistair Pagnamenta, Andrea Wenninger-Weinzier, Maria Fernanda Martinez-Reza, Lukas Landler, Stefano Lise, Jenny C Taylor, Gaetano Terrone, Giuseppina Vitiello, Ennio Del Giudice, Nicola Brunetti-Pierri, Alessandra D’Amico, Alexandre Reymond, Norine Voisin, Jonathan A. Bernstein, Ellyn Farrelly, Usha Kini, Thomas A. Leonard, Stéphanie Valence, Lydie Burglen, Linlea Armstrong, Susan M. Hiatt, Gregory M. Cooper, Kimberly A Aldinger, William B Dobyns, Ghayda Mirzaa, Tyler Mark Pierson, Frank Baas, Jamel Chelly, Nicholas J. Cowan, David Anthony Keays

Neuron. Author manuscript; available in PMC 2019 Dec 19.

Published in final edited form as: Neuron. 2018 Dec 19; 100(6): 1354–1368.e5. Published online 2018 Nov 15. doi: 10.1016/j.neuron.2018.10.044

PMCID:: PMC6436622

Abstract Article PDF–3.6M

Select item 32336542.

Functionally Recurrent Rearrangements of the MAST Kinase and Notch Gene Families in Breast Cancer

Dan R. Robinson, Shanker Kalyana-Sundaram, Yi-Mi Wu, Sunita Shankar, Xuhong Cao, Bushra Ateeq, Irfan A. Asangani, Matthew Iyer, Christopher A. Maher, Catherine S. Grasso, Robert J. Lonigro, Michael Quist, Javed Siddiqui, Rohit Mehra, Xiaojun Jing, Thomas J. Giordano, Michael S. Sabel, Celina G. Kleer, Nallasivam Palanisamy, Rachael Natrajan, Maryou B. Lambros, Jorge S. Reis-Filho, Chandan Kumar-Sinha, Arul M. Chinnaiyan

Nat Med. Author manuscript; available in PMC 2012 Jun 1.

Published in final edited form as: Nat Med. 2011 Dec; 17(12): 1646–1651. Published online 2011 Nov 20. doi: 10.1038/nm.2580

PMCID:: PMC3233654

Abstract Article PDF–1.7M

Select item 68287003.

Targeted resequencing identifies genes with recurrent variation in cerebral palsy

C. L. van Eyk, M. A. Corbett, M. S. B. Frank, D. L. Webber, M. Newman, J. G. Berry, K. Harper, B. P. Haines, G. McMichael, J. A. Woenig, A. H. MacLennan, J. Gecz

NPJ Genom Med. 2019; 4: 27. Published online 2019 Nov 4. doi: 10.1038/s41525-019-0101-z

PMCID:: PMC6828700

Abstract Article PDF–1.3M

Select item 57839394.

Combined chemical genetics and data-driven bioinformatics approach identifies receptor tyrosine kinase inhibitors as host-directed antimicrobials

Cornelis J. Korbee, Matthias T. Heemskerk, Dragi Kocev, Elisabeth van Strijen, Omid Rabiee, Kees L. M. C. Franken, Louis Wilson, Nigel D. L. Savage, Sašo Džeroski, Mariëlle C. Haks, Tom H. M. Ottenhoff

Nat Commun. 2018; 9: 358. Published online 2018 Jan 24. doi: 10.1038/s41467-017-02777-6

PMCID:: PMC5783939

Abstract Article PDF–1.0M

Select item 40070595.

Comparative analysis of RNAi screening technologies at genome-scale reveals an inherent processing inefficiency of the plasmid-based shRNA hairpin

Bhavneet Bhinder, David Shum, Hakim Djaballah

Comb Chem High Throughput Screen. Author manuscript; available in PMC 2014 May 2.

Published in final edited form as: Comb Chem High Throughput Screen. 2014 Feb; 17(2): 98–113. doi: 10.2174/1386207317666140117101852

PMCID:: PMC4007059

Abstract Article PDF–4.1M

Select item 31555676.

Transcriptional Profiling of Human Liver Identifies Sex-Biased Genes Associated with Polygenic Dyslipidemia and Coronary Artery Disease

Yijing Zhang, Kathrin Klein, Aarathi Sugathan, Najlla Nassery, Alan Dombkowski, Ulrich M. Zanger, David J. Waxman

PLoS One. 2011; 6(8): e23506. Published online 2011 Aug 12. doi: 10.1371/journal.pone.0023506

PMCID:: PMC3155567

Abstract Article PDF–707K

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