PMC Links for Nucleotide (Select 1780222505) - PMC

Select item 67277591.

VCP/p97 controls signals of the ERK1/2 pathway transmitted via the Shoc2 scaffolding complex: novel insights into IBMPFD pathology

HyeIn Jang, Eun Ryoung Jang, Patricia G. Wilson, Daniel Anderson, Emilia Galperin

Mol Biol Cell. 2019 Jul 1; 30(14): 1655–1663. doi: 10.1091/mbc.E19-03-0144

PMCID:: PMC6727759

Abstract Article PDF–1.3M

Select item 62467692.

Systematic identification of Celastrol-binding proteins reveals that Shoc2 is inhibited by Celastrol

Huang Xiao-pei, Chen Ji-kuai, Wei Xue, Yi-Fan Dong, Lang Yan, Zhang Xiao-fang, Pan Ya-min, Chang Wen-jun, Zhu Jiang-bo

Biosci Rep. 2018 Dec 21; 38(6): BSR20181233. Prepublished online 2018 Oct 17. Published online 2018 Nov 21. doi: 10.1042/BSR20181233

Correction in:: Biosci Rep. 2021 Apr 30; 41(4): BSR-20181233_COR.

PMCID:: PMC6246769

Abstract Article PDF–922K

Select item 49733163.

Sur8 mediates tumorigenesis and metastasis in colorectal cancer

Young-Mi Lee, Saluja Kaduwal, Kug Hwa Lee, Jong-Chan Park, Woo-Jeong Jeong, Kang-Yell Choi

Exp Mol Med. 2016 Jul; 48(7): e249. Published online 2016 Jul 29. doi: 10.1038/emm.2016.58

PMCID:: PMC4973316

Abstract Article PDF–2.7M

Select item 27654654.

Mutation in SHOC2 promotes aberrant protein N-myristoylation and underlies Noonan-like syndrome with loose anagen hair

Viviana Cordeddu, Elia Di Schiavi, Len A. Pennacchio, Avi Ma'ayan, Anna Sarkozy, Valentina Fodale, Serena Cecchetti, Alessio Cardinale, Joel Martin, Wendy Schackwitz, Anna Lipzen, Giuseppe Zampino, Laura Mazzanti, Maria C. Digilio, Simone Martinelli, Elisabetta Flex, Francesca Lepri, Deborah Bartholdi, Kerstin Kutsche, Giovanni B. Ferrero, Cecilia Anichini, Angelo Selicorni, Cesare Rossi, Romano Tenconi, Martin Zenker, Daniela Merlo, Bruno Dallapiccola, Ravi Iyengar, Paolo Bazzicalupo, Bruce D. Gelb, Marco Tartaglia

Nat Genet. Author manuscript; available in PMC 2010 Mar 1.

Published in final edited form as: Nat Genet. 2009 Sep; 41(9): 1022–1026. Published online 2009 Aug 16. doi: 10.1038/ng.425

PMCID:: PMC2765465

Abstract Article PDF–2.1M

Select item 3165415.

The leucine-rich repeat protein SUR-8 enhances MAP kinase activation and forms a complex with Ras and Raf

Weiquan Li, Min Han, Kun-Liang Guan

Genes Dev. 2000 Apr 15; 14(8): 895–900.

PMCID:: PMC316541

Abstract Article PDF–355K

Select item 226796.

soc-2 encodes a leucine-rich repeat protein implicated in fibroblast growth factor receptor signaling

Laura M. Selfors, Jennifer L. Schutzman, Christina Z. Borland, Michael J. Stern

Proc Natl Acad Sci U S A. 1998 Jun 9; 95(12): 6903–6908. doi: 10.1073/pnas.95.12.6903

PMCID:: PMC22679

Abstract Article PDF–272K

Select item 57257017.

A novel approach using long‐read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders

Maria Wilbe, Sanna Gudmundsson, Josefin Johansson, Adam Ameur, Eva‐Lena Stattin, Göran Annerén, Helena Malmgren, Carina Frykholm, Marie‐Louise Bondeson

Prenat Diagn. 2017 Nov; 37(11): 1146–1154. Published online 2017 Oct 17. doi: 10.1002/pd.5156

PMCID:: PMC5725701

Abstract Article PDF–545K

Select item 46578598.

Candidate genes contributing to the aggressive phenotype of mantle cell lymphoma

Sarah E. Henson, Travis Morford, Mary-Pat Stein, Randolph Wall, Cindy S. Malone

Acta Histochem. Author manuscript; available in PMC 2015 Nov 24.

Published in final edited form as: Acta Histochem. 2011 Nov; 113(7): 729–742. Published online 2010 Dec 9. doi: 10.1016/j.acthis.2010.11.001

PMCID:: PMC4657859

Abstract Article PDF–1.5M

Select item 46422999.

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

Berta Luzón-Toro, Hongsheng Gui, Macarena Ruiz-Ferrer, Clara Sze-Man Tang, Raquel M. Fernández, Pak-Chung Sham, Ana Torroglosa, Paul Kwong-Hang Tam, Laura Espino-Paisán, Stacey S. Cherny, Marta Bleda, María del Valle Enguix-Riego, Joaquín Dopazo, Guillermo Antiñolo, María-Mercé García-Barceló, Salud Borrego

Sci Rep. 2015; 5: 16473. Published online 2015 Nov 12. doi: 10.1038/srep16473

PMCID:: PMC4642299

Abstract Article PDF–729K

Select item 460701310.

Mutation in NRAS in familial Noonan syndrome – case report and review of the literature

Sara Ekvall, Maria Wilbe, Jovanna Dahlgren, Eric Legius, Arie van Haeringen, Otto Westphal, Göran Annerén, Marie-Louise Bondeson

BMC Med Genet. 2015; 16: 95. Published online 2015 Oct 14. doi: 10.1186/s12881-015-0239-1

PMCID:: PMC4607013

Abstract Article PDF–1018K

Select item 459476711.

A conserved set of maternal genes? Insights from a molluscan transcriptome

M. MAUREEN LIU, JOHN W. DAVEY, DANIEL J. JACKSON, MARK L. BLAXTER, ANGUS DAVISON

Int J Dev Biol. Author manuscript; available in PMC 2015 Oct 6.

Published in final edited form as: Int J Dev Biol. 2014; 58(6-8): 501–511. doi: 10.1387/ijdb.140121ad

PMCID:: PMC4594767

Abstract Article PDF–1004K

Select item 418815212.

Clinical and Molecular Findings of Tunisian Patients with RASopathies

Rim Louati, N. Bouayed Abdelmoula, Imen Trabelsi, Dorra Abid, Christina Lissewski, Najla Kharrat, Samir Kamoun, Martin Zenker, Tarek Rebai

Mol Syndromol. 2014 Aug; 5(5): 212–217. Published online 2014 May 23. doi: 10.1159/000362898

PMCID:: PMC4188152

Abstract Article PDF–137K

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