PMC Links for Nucleotide (Select 1609036687) - PMC

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Items: 5

Select item 67426461.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations

Robert Fragoza, Jishnu Das, Shayne D. Wierbowski, Jin Liang, Tina N. Tran, Siqi Liang, Juan F. Beltran, Christen A. Rivera-Erick, Kaixiong Ye, Ting-Yi Wang, Li Yao, Matthew Mort, Peter D. Stenson, David N. Cooper, Xiaomu Wei, Alon Keinan, John C. Schimenti, Andrew G. Clark, Haiyuan Yu

Nat Commun. 2019; 10: 4141. Published online 2019 Sep 12. doi: 10.1038/s41467-019-11959-3

PMCID:: PMC6742646

Abstract Article PDF–1.2M

Select item 62957302.

A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defect

Chan Choo Yap, Laura Digilio, Kamil Kruczek, Matylda Roszkowska, Xiao-qin Fu, Judy S. Liu, Bettina Winckler

J Biol Chem. 2018 Dec 7; 293(49): 18890–18902. Published online 2018 Oct 5. doi: 10.1074/jbc.RA118.004462

PMCID:: PMC6295730

Abstract Article PDF–3.7M

Select item 55956793.

Evidence for reduced neurogenesis in the aging human hippocampus despite stable stem cell markers

Kathryn J. Mathews, Katherine M. Allen, Danny Boerrigter, Helen Ball, Cynthia Shannon Weickert, Kay L. Double

Aging Cell. 2017 Oct; 16(5): 1195–1199. Published online 2017 Aug 1. doi: 10.1111/acel.12641

PMCID:: PMC5595679

Abstract Article PDF–662K

Select item 55078564.

Dynamic microtubule association of Doublecortin X (DCX) is regulated by its C-terminus

Maryam Moslehi, Dominic C. H. Ng, Marie A. Bogoyevitch

Sci Rep. 2017; 7: 5245. Published online 2017 Jul 12. doi: 10.1038/s41598-017-05340-x

PMCID:: PMC5507856

Abstract Article PDF–7.3M

Select item 10508885.

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.

V des Portes, J M Pinard, D Smadja, J Motte, O Boespflüg-Tanguy, M L Moutard, I Desguerre, P Billuart, A Carrie, T Bienvenu, M C Vinet, L Bachner, C Beldjord, O Dulac, A Kahn, G Ponsot, J Chelly

J Med Genet. 1997 Mar; 34(3): 177–183. doi: 10.1136/jmg.34.3.177