PMC Links for Protein (Select 334302894) - PMC

Select item 60755581.

A mutation in IFT43 causes non-syndromic recessive retinal degeneration

Pooja Biswas, Jacque L Duncan, Muhammad Ali, Hiroko Matsui, Muhammad Asif Naeem, Pongali B Raghavendra, Kelly A Frazer, Heleen H Arts, Sheikh Riazuddin, Javed Akram, J Fielding Hejtmancik, S Amer Riazuddin, Radha Ayyagari

Hum Mol Genet. 2017 Dec 1; 26(23): 4741–4751. Published online 2017 Sep 18. doi: 10.1093/hmg/ddx356

PMCID:: PMC6075558

Abstract Article PDF–1.4M

Select item 53872112.

Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia

Ivan Duran, S. Paige Taylor, Wenjuan Zhang, Jorge Martin, Faisal Qureshi, Suzanne M. Jacques, Robert Wallerstein, Ralph S. Lachman, Deborah A. Nickerson, Michael Bamshad, Daniel H. Cohn, Deborah Krakow

Cilia. 2017; 6: 7. Published online 2017 Apr 10. doi: 10.1186/s13630-017-0051-y

PMCID:: PMC5387211

Abstract Article PDF–2.6M

Select item 53417263.

Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein–coupled receptors

Tomoaki Hirano, Yohei Katoh, Kazuhisa Nakayama

Mol Biol Cell. 2017 Feb 1; 28(3): 429–439. doi: 10.1091/mbc.E16-11-0813

PMCID:: PMC5341726

Abstract Article PDF–2.7M

Select item 34120314.

N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB

Petra Van Damme, Marta Lasa, Bogdan Polevoda, Cristina Gazquez, Alberto Elosegui-Artola, Duk Soo Kim, Elena De Juan-Pardo, Kimberly Demeyer, Kristine Hole, Esther Larrea, Evy Timmerman, Jesus Prieto, Thomas Arnesen, Fred Sherman, Kris Gevaert, Rafael Aldabe

Proc Natl Acad Sci U S A. 2012 Jul 31; 109(31): 12449–12454. Published online 2012 Jul 18. doi: 10.1073/pnas.1210303109