PMC Links for GEO Profiles (Select 62204712) - PMC

Select item 69866821.

RIT1 oncoproteins escape LZTR1-mediated proteolysis

Pau Castel, Alice Cheng, Antonio Cuevas-Navarro, David B. Everman, Alex G. Papageorge, Dhirendra K. Simanshu, Alexandra Tankka, Jacqueline Galeas, Anatoly Urisman, Frank McCormick

Science. Author manuscript; available in PMC 2020 Jan 28.

Published in final edited form as: Science. 2019 Mar 15; 363(6432): 1226–1230. doi: 10.1126/science.aav1444

PMCID:: PMC6986682

Abstract Article PDF–1.1M

Select item 65792592.

Rin, a Neuron-Specific and Calmodulin-Binding Small G-Protein, and Rit Define a Novel Subfamily of Ras Proteins

Ching-Hsien J. Lee, Neil G. Della, Christina E. Chew, Donald J. Zack

J Neurosci. 1996 Nov 1; 16(21): 6784–6794. doi: 10.1523/JNEUROSCI.16-21-06784.1996

PMCID:: PMC6579259

Abstract Article

Select item 64913863.

New Noonan syndrome model mice with RIT1 mutation exhibit cardiac hypertrophy and susceptibility to β-adrenergic stimulation-induced cardiac fibrosis

Shingo Takahara, Shin-ichi Inoue, Sachiko Miyagawa-Tomita, Katsuhisa Matsuura, Yasumi Nakashima, Tetsuya Niihori, Yoichi Matsubara, Yoshikatsu Saiki, Yoko Aoki

EBioMedicine. 2019 Apr; 42: 43–53. Published online 2019 Mar 18. doi: 10.1016/j.ebiom.2019.03.014

PMCID:: PMC6491386

Abstract Article PDF–2.5M

Select item 61972794.

RIT1 suppresses esophageal squamous cell carcinoma growth and metastasis and predicts good prognosis

Yan-Fen Feng, Yi-Yan Lei, Jia-Bin Lu, Shao-Yan Xi, Yu Zhang, Qi-Tao Huang, Qiu-Liang Wu, Fang Wang

Cell Death Dis. 2018 Nov; 9(11): 1085. Published online 2018 Oct 22. doi: 10.1038/s41419-018-0979-x

PMCID:: PMC6197279

Abstract Article PDF–2.8M

Select item 49706875.

Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia

Hélène Cavé, Aurélie Caye, Nehla Ghedira, Yline Capri, Nathalie Pouvreau, Natacha Fillot, Aurélien Trimouille, Cédric Vignal, Odile Fenneteau, Yves Alembik, Jean-Luc Alessandri, Patricia Blanchet, Odile Boute, Patrice Bouvagnet, Albert David, Anne Dieux Coeslier, Bérénice Doray, Olivier Dulac, Valérie Drouin-Garraud, Marion Gérard, Delphine Héron, Bertrand Isidor, Didier Lacombe, Stanislas Lyonnet, Laurence Perrin, Marlène Rio, Joëlle Roume, Sylvie Sauvion, Annick Toutain, Catherine Vincent-Delorme, Marjorie Willems, Clarisse Baumann, Alain Verloes

Eur J Hum Genet. 2016 Aug; 24(8): 1124–1131. Published online 2016 Jan 13. doi: 10.1038/ejhg.2015.273

PMCID:: PMC4970687

Abstract Article PDF–1.4M

Select item 41281296.

Next-generation sequencing identifies rare variants associated with Noonan syndrome

Peng-Chieh Chen, Jiani Yin, Hui-Wen Yu, Tao Yuan, Minerva Fernandez, Christina K. Yung, Quang M. Trinh, Vanya D. Peltekova, Jeffrey G. Reid, Erica Tworog-Dube, Margaret B. Morgan, Donna M. Muzny, Lincoln Stein, John D. McPherson, Amy E. Roberts, Richard A. Gibbs, Benjamin G. Neel, Raju Kucherlapati

Proc Natl Acad Sci U S A. 2014 Aug 5; 111(31): 11473–11478. Published online 2014 Jul 21. doi: 10.1073/pnas.1324128111

PMCID:: PMC4128129

Abstract Article PDF–910K

Select item 37107677.

Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome

Yoko Aoki, Tetsuya Niihori, Toshihiro Banjo, Nobuhiko Okamoto, Seiji Mizuno, Kenji Kurosawa, Tsutomu Ogata, Fumio Takada, Michihiro Yano, Toru Ando, Tadataka Hoshika, Christopher Barnett, Hirofumi Ohashi, Hiroshi Kawame, Tomonobu Hasegawa, Takahiro Okutani, Tatsuo Nagashima, Satoshi Hasegawa, Ryo Funayama, Takeshi Nagashima, Keiko Nakayama, Shin-ichi Inoue, Yusuke Watanabe, Toshihiko Ogura, Yoichi Matsubara

Am J Hum Genet. 2013 Jul 11; 93(1): 173–180. doi: 10.1016/j.ajhg.2013.05.021

PMCID:: PMC3710767

Abstract Article PDF–913K

Select item 31780598.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

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