PMC Links for GEO Profiles (Select 69963945) - PMC

Select item 36824031.

Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes

Sulochana Devi, Yogananda Markandeya, Nityanand Maddodi, Anuradha Dhingra, Noga Vardi, Ravi C Balijepalli, Vijayasaradhi Setaluri

Pigment Cell Melanoma Res. Author manuscript; available in PMC 2014 May 1.

Published in final edited form as: Pigment Cell Melanoma Res. 2013 May; 26(3): 348–356. Published online 2013 Mar 27. doi: 10.1111/pcmr.12083

PMCID:: PMC3682403

Abstract Article PDF–1.3M

Select item 32066412.

Genetic variants in Transient Receptor Potential cation channel, subfamily M 1 (TRPM1) and their risk of albuminuria-related traits in Mexican Americans

Farook Thameem, Sobha Puppala, Nedal H. Arar, John Blangero, Ravindranath Duggirala, Hanna E. Abboud

Clin Chim Acta. Author manuscript; available in PMC 2012 Nov 20.

Published in final edited form as: Clin Chim Acta. 2011 Nov 20; 412(23-24): 2058–2062. Published online 2011 Apr 1. doi: 10.1016/j.cca.2011.03.024

PMCID:: PMC3206641

Abstract Article PDF–553K

Select item 31780593.

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

Select item 29687144.

Mouse Model Resources for Vision Research

Jungyeon Won, Lan Ying Shi, Wanda Hicks, Jieping Wang, Ronald Hurd, Jürgen K. Naggert, Bo Chang, Patsy M. Nishina

J Ophthalmol. 2011; 2011: 391384. Published online 2010 Oct 31. doi: 10.1155/2011/391384

PMCID:: PMC2968714

Abstract Article PDF–5.7M

Select item 28067055.

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade

Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani, Hiroshi Ueda, Mineo Kondo, Yasuo Mori, Masao Tachibana, Takahisa Furukawa

Proc Natl Acad Sci U S A. 2010 Jan 5; 107(1): 332–337. Published online 2009 Dec 29. doi: 10.1073/pnas.0912730107

PMCID:: PMC2806705

Abstract Article PDF–1.9M

Select item 27764196.

TRPM1 is required for the depolarizing light response in retinal ON-bipolar cells

Catherine W. Morgans, Jianmei Zhang, Brett G. Jeffrey, Steve M. Nelson, Neal S. Burke, Robert M. Duvoisin, R. Lane Brown

Proc Natl Acad Sci U S A. 2009 Nov 10; 106(45): 19174–19178. Published online 2009 Oct 27. doi: 10.1073/pnas.0908711106

PMCID:: PMC2776419

Abstract Article PDF–1.2M

Select item 27758337.

Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans

Zheng Li, Panagiotis I. Sergouniotis, Michel Michaelides, Donna S. Mackay, Genevieve A. Wright, Sophie Devery, Anthony T. Moore, Graham E. Holder, Anthony G. Robson, Andrew R. Webster

Am J Hum Genet. 2009 Nov 13; 85(5): 711–719. doi: 10.1016/j.ajhg.2009.10.003

PMCID:: PMC2775833

Abstract Article PDF–1.3M

Select item 27758308.

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Susanne Kohl, Bart P. Leroy, Francis L. Munier, Xavier Guillonneau, Saddek Mohand-Saïd, Kinga Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus Preising, Ulrich Kellner, Agnes B. Renner, Antje Bernd, Aline Antonio, Veselina Moskova-Doumanova, Marie-Elise Lancelot, Charlotte M. Poloschek, Isabelle Drumare, Sabine Defoort-Dhellemmes, Bernd Wissinger, Thierry Léveillard, Christian P. Hamel, Daniel F. Schorderet, Elfride De Baere, Wolfgang Berger, Samuel G. Jacobson, Eberhart Zrenner, José-Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz

Am J Hum Genet. 2009 Nov 13; 85(5): 720–729. doi: 10.1016/j.ajhg.2009.10.013

PMCID:: PMC2775830

Abstract Article PDF–760K

Select item 27758269.

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

Maria M. van Genderen, Mieke M.C. Bijveld, Yvonne B. Claassen, Ralph J. Florijn, Jillian N. Pearring, Francoise M. Meire, Maureen A. McCall, Frans C.C. Riemslag, Ronald G. Gregg, Arthur A.B. Bergen, Maarten Kamermans

Am J Hum Genet. 2009 Nov 13; 85(5): 730–736. doi: 10.1016/j.ajhg.2009.10.012

PMCID:: PMC2775826

Abstract Article PDF–1.0M

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