WFS1 (Estonian Wikipedia)

Analysis of information sources in references of the Wikipedia article "WFS1" in Estonian language version.

refsWebsite

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4^th place

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3oxfordjournals.org

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4,380^th place

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3,242^nd place

1chemistryexplained.com

low place

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1web.archive.org

1^st place

1^st place

1proteinatlas.org

low place

low place

chemistryexplained.com

Transmembrane Protein (vaadatud 17.10.16)

ensembl.org

Gene: WFS1 ENSG00000109501 eEnsembl (vaadatud 17.10.16)

nih.gov

ncbi.nlm.nih.gov

HomoloGene:4380. Gene conserved in Bilateria (vaadatud 29. novembril 2016)
WFS1 wolframin ER transmembrane glycoprotein ( Homo sapiens (human) ) (vaadatud 17.10.16)
Çelmeli, G., Türkkahraman, D., Çürek, Y., Houghton, J., Akçurin, S. and Bircan, İ., 2016. Clinical and molecular genetic analysis in three children with Wolfram Syndrome: a novel WFS1 mutation (c. 2534T> A) Journal of clinical research in pediatric endocrinology.
Shi, S. M., Han, Y. H. ja Wang, H. B. (2016). Research progress of mutational spectrum and pathophysiology of WFS1 gene in Wolfram syndrome and nonsyndromic low frequency sensorineural hearing loss Zhonghua er bi yan hou tou jing wai ke za zhi= Chinese journal of otorhinolaryngology head and neck surgery, 51(9), lk 712.

ghr.nlm.nih.gov

Wolfram syndrome (vaadatud 17.10.16)

omim.org

WFS1 GENE; WFS1 OMIM (vaadatud 17.10.16)

oxfordjournals.org

hmg.oxfordjournals.org

Strom, T. M., Hortnagel, K., Hofmann, S., Gekeler, F., Scharfe, C., Rabl, W., Gerbitz, K. D., Meitinger, T. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein Hum. Molec. Genet. 7: 2021–2028, 1998.
Zatyka, M., Ricketts, C., da Silva Xavier, G., Minton, J., Fenton, S., Hofmann-Thiel, S., Rutter, G.A. ja Barrett, T.G. (2008). Sodium-potassium ATPase β1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress Human molecular genetics, 17(2), lk 190–200.
Takeda, K., Inoue, K., Tanizawa, Y., Matsuzaki, Y., Oba, J., Watanabe Y., Shinoda, K., Oka, Y. WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain Hum. Molec. Genet. 10: 477–484, 2001.

proteinatlas.org

WFS1 The Human Protein Atlas (vaadatud 17.10.16)

vcu.edu

people.vcu.edu

"Measurement of bleeding and healing time in knockout mice with WFS2", Neda Niazi, 2. detsember 2012. pdf-dokument

web.archive.org

V. Viswanathan, S. Medempudi ja M. Kadiri: Wolfram Syndrome (vaadatud 17.10.16)