PMC Links for Nucleotide (Select 13929175) - PMC

Select item 61988161.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Irina N. Bespalova, Guy Van Camp, Steven J.H. Bom, David J. Brown, Kim Cryns, Andrew T. DeWan, Ayse E. Erson, Kris Flothmann, Henricus P.M. Kunst, Purnima Kurnool, Theru A. Sivakumaran, Cor W.R.J. Cremers, Suzanne M. Leal, Margit Burmeister, Marci M. Lesperance

Hum Mol Genet. Author manuscript; available in PMC 2018 Oct 23.

Published in final edited form as: Hum Mol Genet. 2001 Oct 15; 10(22): 2501–2508. doi: 10.1093/hmg/10.22.2501

PMCID:: PMC6198816

Abstract Article PDF–1.1M

Select item 55792612.

Wfs1- deficient rats develop primary symptoms of Wolfram syndrome: insulin-dependent diabetes, optic nerve atrophy and medullary degeneration

Mario Plaas, Kadri Seppa, Riin Reimets, Toomas Jagomäe, Maarja Toots, Tuuliki Koppel, Tuuli Vallisoo, Mait Nigul, Indrek Heinla, Riho Meier, Allen Kaasik, Andres Piirsoo, Miriam A. Hickey, Anton Terasmaa, Eero Vasar

Sci Rep. 2017; 7: 10220. Published online 2017 Aug 31. doi: 10.1038/s41598-017-09392-x

PMCID:: PMC5579261

Abstract Article PDF–7.9M

Select item 31435433.

A WFS1 Haplotype Consisting of the Minor Alleles of rs752854, rs10010131, and rs734312 Shows a Protective Role Against Type 2 Diabetes in Russian Patients

Dimitry A Chistiakov, Dmitry S. Khodyrev, Svetlana A. Smetanina, Larisa N. Bel'chikova, Lyudmila A. Suplotova, Valery V. Nosikov

Rev Diabet Stud. 2010 Winter; 7(4): 285–292. Published online 2011 Feb 10. doi: 10.1900/RDS.2010.7.285

PMCID:: PMC3143543

Abstract Article PDF–138K

Select item 31003664.

Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment

Nanna D. Rendtorff, Marianne Lodahl, Houda Boulahbel, Ida R. Johansen, Arti Pandya, Katherine O. Welch, Virginia W. Norris, Kathleen S. Arnos, Maria Bitner-Glindzicz, Sarah B. Emery, Marilyn B. Mets, Toril Fagerheim, Kristina Eriksson, Lars Hansen, Helene Bruhn, Claes Möller, Sture Lindholm, Stefan Ensgård, Marci M. Lesperance, Lisbeth Tranebjærg

Am J Med Genet A. Author manuscript; available in PMC 2012 Jun 1.

Published in final edited form as: Am J Med Genet A. 2011 Jun; 155(6): 1298–1313. Published online 2011 Apr 28. doi: 10.1002/ajmg.a.33970

PMCID:: PMC3100366

Abstract Article PDF–939K

Select item 28279485.

Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells

Sonya G. Fonseca, Shinsuke Ishigaki, Christine M. Oslowski, Simin Lu, Kathryn L. Lipson, Rajarshi Ghosh, Emiko Hayashi, Hisamitsu Ishihara, Yoshitomo Oka, M. Alan Permutt, Fumihiko Urano

J Clin Invest. 2010 Mar 1; 120(3): 744–755. Published online 2010 Feb 15. doi: 10.1172/JCI39678

PMCID:: PMC2827948

Abstract Article PDF–4.3M

Select item 69527866.

Exercise Exacerbates the Transcriptional Profile of Hypoxia, Oxidative Stress and Inflammation in Rats with Adjuvant-Induced Arthritis

Susana Aideé González-Chávez, Celia María Quiñonez-Flores, Gerardo Pavel Espino-Solís, José Ángel Vázquez-Contreras, César Pacheco-Tena

Cells. 2019 Dec; 8(12): 1493. Published online 2019 Nov 22. doi: 10.3390/cells8121493

PMCID:: PMC6952786

Abstract Article PDF–3.0M

Select item 55664867.

Compulsive methamphetamine taking in the presence of punishment is associated with increased oxytocin expression in the nucleus accumbens of rats

Irina N. Krasnova, Maria Carla Gerra, Donna Walther, Subramaniam Jayanthi, Bruce Ladenheim, Michael T. McCoy, Christie Brannock, Jean Lud Cadet

Sci Rep. 2017; 7: 8331. Published online 2017 Aug 21. doi: 10.1038/s41598-017-08898-8

PMCID:: PMC5566486

Abstract Article PDF–1.9M

Select item 49510538.

Role of Mitochondrial Dynamics in Neuronal Development: Mechanism for Wolfram Syndrome

Michal Cagalinec, Mailis Liiv, Zuzana Hodurova, Miriam Ann Hickey, Annika Vaarmann, Merle Mandel, Akbar Zeb, Vinay Choubey, Malle Kuum, Dzhamilja Safiulina, Eero Vasar, Vladimir Veksler, Allen Kaasik

PLoS Biol. 2016 Jul; 14(7): e1002511. Published online 2016 Jul 19. doi: 10.1371/journal.pbio.1002511

PMCID:: PMC4951053

Abstract Article PDF–4.4M

Select item 48952539.

Comparative transcriptional profiling of renal cortex in rats with inherited stress-induced arterial hypertension and normotensive Wistar Albino Glaxo rats

Larisa A. Fedoseeva, Marina A. Ryazanova, Nikita I. Ershov, Arcady L. Markel, Olga E. Redina

BMC Genet. 2016; 17(Suppl 1): 12. Published online 2016 Jan 27. doi: 10.1186/s12863-015-0306-9

PMCID:: PMC4895253

Abstract Article PDF–530K

Select item 305719610.

Identification of Potentially Neuroprotective Genes Upregulated by Neurotrophin Treatment of CA3 Neurons in the Injured Brain

Saafan Z. Malik, Shahab Motamedi, Nicolas C. Royo, David LeBold, Deborah J. Watson

J Neurotrauma. 2011 Mar; 28(3): 415–430. doi: 10.1089/neu.2010.1487

PMCID:: PMC3057196

Abstract Article PDF–592K

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