PMC Links for Nucleotide (Select 1519314703) - PMC

Select item 39623601.

Subcellular Fractionation and Localization Studies Reveal a Direct Interaction of the Fragile X Mental Retardation Protein (FMRP) with Nucleolin

Mohamed S. Taha, Kazem Nouri, Lech G. Milroy, Jens M. Moll, Christian Herrmann, Luc Brunsveld, Roland P. Piekorz, Mohammad R. Ahmadian

PLoS One. 2014; 9(3): e91465. Published online 2014 Mar 21. doi: 10.1371/journal.pone.0091465

PMCID:: PMC3962360

Abstract Article PDF–5.5M

Select item 11715172.

Increased apoptosis induction by 121F mutant p53.

E Saller, E Tom, M Brunori, M Otter, A Estreicher, D H Mack, R Iggo

EMBO J. 1999 Aug 16; 18(16): 4424–4437. doi: 10.1093/emboj/18.16.4424

PMCID:: PMC1171517

Summary PDF–575K

Select item 11704463.

In mouse brain profilin I and profilin II associate with regulators of the endocytic pathway and actin assembly.

W Witke, A V Podtelejnikov, A Di Nardo, J D Sutherland, C B Gurniak, C Dotti, M Mann

EMBO J. 1998 Feb 16; 17(4): 967–976. doi: 10.1093/emboj/17.4.967

PMCID:: PMC1170446

Summary PDF–439K

Select item 375234.

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

Annette Schenck, Barbara Bardoni, Annamaria Moro, Claudia Bagni, Jean-Louis Mandel

Proc Natl Acad Sci U S A. 2001 Jul 17; 98(15): 8844–8849. Published online 2001 Jul 3. doi: 10.1073/pnas.151231598

PMCID:: PMC37523

Abstract Article PDF–531K

Select item 70179795.

Early diagnosis improving the outcome of an infant with epileptic encephalopathy with cytoplasmic FMRP interacting protein 2 mutation: Case report and literature review

Min Zhong, Shuang Liao, Tingsong Li, Peng Wu, Yanqin Wang, Fangrui Wu, Xiujuan Li, Siqi Hong, Lisi Yan, Li Jiang

Medicine (Baltimore) 2019 Nov; 98(44): e17749. Published online 2019 Nov 1. doi: 10.1097/MD.0000000000017749

PMCID:: PMC7017979

Abstract Article PDF–1.2M

Select item 64898716.

Novel West syndrome candidate genes in a Chinese cohort

Jing Peng, Ying Wang, Fang He, Chen Chen, Li‐Wen Wu, Li‐Fen Yang, Yu‐Ping Ma, Wen Zhang, Zi‐Qing Shi, Chao Chen, Kun Xia, Hui Guo, Fei Yin, Nan Pang

CNS Neurosci Ther. 2018 Dec; 24(12): 1196–1206. Published online 2018 Apr 17. doi: 10.1111/cns.12860

PMCID:: PMC6489871

Abstract Article PDF–1.0M

Select item 59850667.

Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder

Chuphong Thongnak, Areerat Hnoonual, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Wasun Chantratita, Pornprot Limprasert, Chonlaphat Sukasem

Int J Genomics. 2018; 2018: 8231547. Published online 2018 May 17. doi: 10.1155/2018/8231547

PMCID:: PMC5985066

Abstract Article PDF–1.0M

Select item 32415098.

Protein complexes containing CYFIP/Sra/PIR121 coordinate ARF1 and RAC1 signaling during clathrin-AP-1-coated carrier biogenesis at the TGN

Mihaela ANITEI, Christoph STANGE, Irina PARSHINA, Thorsten BAUST, Annette SCHENCK, Graça RAPOSO, Tomas KIRCHHAUSEN, Bernard HOFLACK

Nat Cell Biol. Author manuscript; available in PMC 2011 Dec 16.

Published in final edited form as: Nat Cell Biol. 2010 Apr; 12(4): 330–340. Published online 2010 Mar 14. doi: 10.1038/ncb2034

Correction in:: volume 12 on page 520

PMCID:: PMC3241509

Abstract Article PDF–4.1M

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