PMC Links for Protein (Select 30181246) - PMC

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

PMCID:: PMC1050888

Summary Page Browse PDF–1.5M

Select item 30103966.

Allelic diversity in human developmental neurogenetics: insights into biology and disease

Christopher A. Walsh, Elizabeth C. Engle

Neuron. Author manuscript; available in PMC 2011 Apr 21.

Published in final edited form as: Neuron. 2010 Oct 21; 68(2): 245–253. doi: 10.1016/j.neuron.2010.09.042

PMCID:: PMC3010396

Abstract Article PDF–428K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 6

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity