PMC Links for Nucleotide (Select 1519244162) - PMC

Result Filters

Links from Nucleotide

Items: 17

Select item 65576181.

Heterogeneity in Mitogen-Activated Protein Kinase (MAPK) Pathway Activation in Uveal Melanoma With Somatic GNAQ and GNA11 Mutations

Getachew Boru, Colleen M. Cebulla, Klarke M. Sample, James B. Massengill, Frederick H. Davidorf, Mohamed H. Abdel-Rahman

Invest Ophthalmol Vis Sci. 2019 Jun; 60(7): 2474–2480. doi: 10.1167/iovs.18-26452

PMCID:: PMC6557618

Abstract Article PDF–1.2M

Select item 62340972.

GNAS, GNAQ and GNA11 Alterations in Patients with Diverse Cancers

Parish AJ, Nguyen V, Goodman A, Murugesan K, Frampton G, Kurzrock R

Cancer. Author manuscript; available in PMC 2019 Oct 15.

Published in final edited form as: Cancer. 2018 Oct 15; 124(20): 4080–4089. Published online 2018 Sep 11. doi: 10.1002/cncr.31724

PMCID:: PMC6234097

Abstract Article PDF–939K

Select item 61512933.

Uveal melanoma driver mutations in GNAQ/11 yield numerous changes in melanocyte biology.

Dahlia E. Perez, Andrea M. Henle, Adam Amsterdam, Hannah R. Hagen, DR. Jacqueline A. Lees

Pigment Cell Melanoma Res. Author manuscript; available in PMC 2019 Sep 1.

Published in final edited form as: Pigment Cell Melanoma Res. 2018 Sep; 31(5): 604–613. Published online 2018 Apr 6. doi: 10.1111/pcmr.12700

PMCID:: PMC6151293

Abstract Article PDF–956K

Select item 11362384.

Ca2+ signalling in K562 human erythroleukaemia cells: effect of dimethyl sulphoxide and role of G-proteins in thrombin- and thromboxane A2-activated pathways.

C P Thomas, M J Dunn, R Mattera

Biochem J. 1995 Nov 15; 312(Pt 1): 151–158. doi: 10.1042/bj3120151

PMCID:: PMC1136238

Summary Page Browse PDF–1.7M

Select item 515625.

Guanine nucleotide-binding regulatory proteins in retinal pigment epithelial cells.

M Jiang, S Pandey, V T Tran, H K Fong

Proc Natl Acad Sci U S A. 1991 May 1; 88(9): 3907–3911. doi: 10.1073/pnas.88.9.3907

PMCID:: PMC51562

Summary Page Browse PDF–1.2M

Select item 66120716.

Clinical mutational profiling and categorization of BRAF mutations in melanomas using next generation sequencing

Parvez M. Lokhandwala, Li-Hui Tseng, Erika Rodriguez, Gang Zheng, Aparna Pallavajjalla, Christopher D. Gocke, James R. Eshleman, Ming-Tseh Lin

BMC Cancer. 2019; 19: 665. Published online 2019 Jul 5. doi: 10.1186/s12885-019-5864-1

PMCID:: PMC6612071

Abstract Article PDF–738K

Select item 58132717.

Cinacalcet Rectifies Hypercalcemia in a Patient With Familial Hypocalciuric Hypercalcemia Type 2 (FHH2) Caused by a Germline Loss‐of‐Function Gα₁₁ Mutation

Caroline M Gorvin, Fadil M Hannan, Treena Cranston, Helena Valta, Outi Makitie, Camilla Schalin‐Jantti, Rajesh V Thakker

J Bone Miner Res. 2018 Jan; 33(1): 32–41. Published online 2017 Sep 22. doi: 10.1002/jbmr.3241

PMCID:: PMC5813271

Abstract Article PDF–1.8M

Select item 57897598.

The role of Gα_q/Gα₁₁ signaling in intestinal epithelial cells

Hirosato Mashima, Noboru Watanabe, Masanari Sekine, Satohiro Matsumoto, Takeharu Asano, Kazuhito Yuhashi, Noriyoshi Sagihara, Shunsuke Urayoshi, Takeshi Uehara, Junichi Fujiwara, Takehiro Ishii, Rumiko Tsuboi, Hiroyuki Miyatani, Hirohide Ohnishi

Biochem Biophys Rep. 2018 Mar; 13: 93–98. Published online 2018 Jan 28. doi: 10.1016/j.bbrep.2018.01.003

PMCID:: PMC5789759

Abstract Article PDF–902K

Select item 53897939.

Mobile Genome Express (MGE): A comprehensive automatic genetic analyses pipeline with a mobile device

Jun-Hee Yoon, Thomas W. Kim, Pedro Mendez, David M. Jablons, Il-Jin Kim

PLoS One. 2017; 12(4): e0174696. Published online 2017 Apr 12. doi: 10.1371/journal.pone.0174696

PMCID:: PMC5389793

Abstract Article PDF–2.2M

Select item 494965010.

A G‐protein Subunit‐α11 Loss‐of‐Function Mutation, Thr54Met, Causes Familial Hypocalciuric Hypercalcemia Type 2 (FHH2)

Caroline M Gorvin, Treena Cranston, Fadil M Hannan, Nigel Rust, Asjid Qureshi, M Andrew Nesbit, Rajesh V Thakker

J Bone Miner Res. 2016 Jun; 31(6): 1200–1206. Published online 2016 Feb 6. doi: 10.1002/jbmr.2778

PMCID:: PMC4949650

Abstract Article PDF–2.2M

Select item 393750911.

Molecular genetic testing of uveal melanoma from routinely processed and stained cytology specimens

Benjamin N. Christopher, Colleen M. Cebulla, Paul E. Wakely, Jr., Frederick H. Davidorf, Mohamed H. Abdel-Rahman

Exp Eye Res. Author manuscript; available in PMC 2014 Feb 28.

Published in final edited form as: Exp Eye Res. 2011 Nov; 93(5): 720–725. Published online 2011 Sep 17. doi: 10.1016/j.exer.2011.09.004

PMCID:: PMC3937509

Abstract Article PDF–1.3M

Select item 349567312.

Genome-wide analysis of pain-, nerve- and neurotrophin -related gene expression in the degenerating human annulus

Helen E Gruber, Gretchen L Hoelscher, Jane A Ingram, Edward N Hanley, Jr

Mol Pain. 2012; 8: 63. Published online 2012 Sep 10. doi: 10.1186/1744-8069-8-63

PMCID:: PMC3495673

Abstract Article PDF–654K

Select item 341311013.

Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimens

Shawn E. Yost, Erin N. Smith, Richard B. Schwab, Lei Bao, HyunChul Jung, Xiaoyun Wang, Emile Voest, John P. Pierce, Karen Messer, Barbara A. Parker, Olivier Harismendy, Kelly A. Frazer

Nucleic Acids Res. 2012 Aug; 40(14): e107. Published online 2012 Apr 6. doi: 10.1093/nar/gks299

PMCID:: PMC3413110

Abstract Article PDF–4.1M

Select item 304083214.

Novel somatic mutations in heterotrimeric G proteins in melanoma

L Isabel Cárdenas-Navia, Pedro Cruz, Jimmy C Lin, NISC Comparative Sequencing Program, Steven A Rosenberg, Yardena Samuels

Cancer Biol Ther. 2010 Jul 1; 10(1): 33–37. Published online 2010 Jul 1. doi: 10.4161/cbt.10.1.11949

PMCID:: PMC3040832

Abstract Article PDF–828K

Select item 286159915.

HOXB13, a Target of DNMT3B, Is Methylated at an Upstream CpG Island, and Functions as a Tumor Suppressor in Primary Colorectal Tumors

Kalpana Ghoshal, Tasneem Motiwala, Rainer Claus, Pearlly Yan, Huban Kutay, Jharna Datta, Sarmila Majumder, Shoumei Bai, Arnab Majumder, Tim Huang, Christoph Plass, Samson T. Jacob

PLoS One. 2010; 5(4): e10338. Published online 2010 Apr 29. doi: 10.1371/journal.pone.0010338