Wolframin (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Wolframin" in Catalan language version.

refsWebsite

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9doi.org

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9worldcat.org

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5nih.gov

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1uniprot.org

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1sciencemag.org

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1isciii.es

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1ub.edu

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1sciencedirect.com

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doi.org

dx.doi.org

Pallotta, Maria Teresa; Tascini, Giorgia; Crispoldi, Roberta; Orabona, Ciriana; Mondanelli, Giada «Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives». Journal of Translational Medicine, 17, 23-07-2019. DOI: 10.1186/s12967-019-1993-1. ISSN: 1479-5876. PMC: 6651977. PMID: 31337416.
Takeda, K. «WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain». Human Molecular Genetics, 10, 5, 01-03-2001, pàg. 477–484. DOI: 10.1093/hmg/10.5.477. ISSN: 1460-2083.
Inoue, Hiroshi; Tanizawa, Yukio; Wasson, Jon; Behn, Philip; Kalidas, Kamini «A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)». Nature Genetics, 20, 2, 1998-10, pàg. 143–148. DOI: 10.1038/2441. ISSN: 1061-4036.
Fonseca, Sonya G.; Fukuma, Mariko; Lipson, Kathryn L.; Nguyen, Linh X.; Allen, Jenny R. «WFS1 Is a Novel Component of the Unfolded Protein Response and Maintains Homeostasis of the Endoplasmic Reticulum in Pancreatic β-Cells». Journal of Biological Chemistry, 280, 47, 29-09-2005, pàg. 39609–39615. DOI: 10.1074/jbc.m507426200. ISSN: 0021-9258.
Osman, Abdullah A.; Saito, Mitsuyoshi; Makepeace, Carol; Permutt, M. Alan; Schlesinger, Paul «Wolframin Expression Induces Novel Ion Channel Activity in Endoplasmic Reticulum Membranes and Increases Intracellular Calcium». Journal of Biological Chemistry, 278, 52, 03-10-2003, pàg. 52755–52762. DOI: 10.1074/jbc.m310331200. ISSN: 0021-9258.
Angebault, Claire; Fauconnier, Jérémy; Patergnani, Simone; Rieusset, Jennifer; Danese, Alberto «ER-mitochondria cross-talk is regulated by the Ca 2+ sensor NCS1 and is impaired in Wolfram syndrome» (en anglès). Science Signaling, 11, 553, 23-10-2018, pàg. eaaq1380. DOI: 10.1126/scisignal.aaq1380. ISSN: 1945-0877.
Strom, T. «Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein». Human Molecular Genetics, 7, 13, 01-12-1998, pàg. 2021–2028. DOI: 10.1093/hmg/7.13.2021. ISSN: 1460-2083.
Esteban Bueno, Gema; Ruano García, Mónica; Grandes Velasco, Sonia; Villar Gómez de las Heras, Karina «Una familia con síndrome de Wolfram». Revista Clínica de Medicina de Familia, 6, 1, 2013-2, pàg. 54–57. DOI: 10.4321/S1699-695X2013000100011. ISSN: 1699-695X.
Yamaguchi, Suguru; Ishihara, Hisamitsu; Tamura, Akira; Yamada, Takahiro; Takahashi, Rui «Endoplasmic reticulum stress and N-glycosylation modulate expression of WFS1 protein». Biochemical and Biophysical Research Communications, 325, 1, 03-12-2004, pàg. 250–256. DOI: 10.1016/j.bbrc.2004.10.017. ISSN: 0006-291X. PMID: 15522226.

isciii.es

scielo.isciii.es

Esteban Bueno, Gema; Ruano García, Mónica; Grandes Velasco, Sonia; Villar Gómez de las Heras, Karina «Una familia con síndrome de Wolfram». Revista Clínica de Medicina de Familia, 6, 1, 2013-2, pàg. 54–57. DOI: 10.4321/S1699-695X2013000100011. ISSN: 1699-695X.

nih.gov

ncbi.nlm.nih.gov

Pallotta, Maria Teresa; Tascini, Giorgia; Crispoldi, Roberta; Orabona, Ciriana; Mondanelli, Giada «Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives». Journal of Translational Medicine, 17, 23-07-2019. DOI: 10.1186/s12967-019-1993-1. ISSN: 1479-5876. PMC: 6651977. PMID: 31337416.
Yamaguchi, Suguru; Ishihara, Hisamitsu; Tamura, Akira; Yamada, Takahiro; Takahashi, Rui «Endoplasmic reticulum stress and N-glycosylation modulate expression of WFS1 protein». Biochemical and Biophysical Research Communications, 325, 1, 03-12-2004, pàg. 250–256. DOI: 10.1016/j.bbrc.2004.10.017. ISSN: 0006-291X. PMID: 15522226.

ghr.nlm.nih.gov

Reference, Genetics Home. «Wolfram syndrome» (en anglès). [Consulta: 25 octubre 2019].
Reference, Genetics Home. «WFS1 gene» (en anglès). [Consulta: 24 octubre 2019].

rarediseases.info.nih.gov

«Síndrome de Wolfram | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program». [Consulta: 25 octubre 2019].

sciencedirect.com

«Protein Synthesis - an overview | ScienceDirect Topics». [Consulta: 24 octubre 2019].

sciencemag.org

stke.sciencemag.org

Angebault, Claire; Fauconnier, Jérémy; Patergnani, Simone; Rieusset, Jennifer; Danese, Alberto «ER-mitochondria cross-talk is regulated by the Ca 2+ sensor NCS1 and is impaired in Wolfram syndrome» (en anglès). Science Signaling, 11, 553, 23-10-2018, pàg. eaaq1380. DOI: 10.1126/scisignal.aaq1380. ISSN: 1945-0877.

ub.edu

sso.ub.edu

«Inici sessió - Identificació UB - Universitat de Barcelona». [Consulta: 24 octubre 2019].

uniprot.org

«WFS1 - Wolframin - Homo sapiens (Human) - WFS1 gene & protein». [Consulta: 24 octubre 2019].

worldcat.org

Pallotta, Maria Teresa; Tascini, Giorgia; Crispoldi, Roberta; Orabona, Ciriana; Mondanelli, Giada «Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives». Journal of Translational Medicine, 17, 23-07-2019. DOI: 10.1186/s12967-019-1993-1. ISSN: 1479-5876. PMC: 6651977. PMID: 31337416.
Takeda, K. «WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain». Human Molecular Genetics, 10, 5, 01-03-2001, pàg. 477–484. DOI: 10.1093/hmg/10.5.477. ISSN: 1460-2083.
Inoue, Hiroshi; Tanizawa, Yukio; Wasson, Jon; Behn, Philip; Kalidas, Kamini «A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)». Nature Genetics, 20, 2, 1998-10, pàg. 143–148. DOI: 10.1038/2441. ISSN: 1061-4036.
Fonseca, Sonya G.; Fukuma, Mariko; Lipson, Kathryn L.; Nguyen, Linh X.; Allen, Jenny R. «WFS1 Is a Novel Component of the Unfolded Protein Response and Maintains Homeostasis of the Endoplasmic Reticulum in Pancreatic β-Cells». Journal of Biological Chemistry, 280, 47, 29-09-2005, pàg. 39609–39615. DOI: 10.1074/jbc.m507426200. ISSN: 0021-9258.
Osman, Abdullah A.; Saito, Mitsuyoshi; Makepeace, Carol; Permutt, M. Alan; Schlesinger, Paul «Wolframin Expression Induces Novel Ion Channel Activity in Endoplasmic Reticulum Membranes and Increases Intracellular Calcium». Journal of Biological Chemistry, 278, 52, 03-10-2003, pàg. 52755–52762. DOI: 10.1074/jbc.m310331200. ISSN: 0021-9258.
Angebault, Claire; Fauconnier, Jérémy; Patergnani, Simone; Rieusset, Jennifer; Danese, Alberto «ER-mitochondria cross-talk is regulated by the Ca 2+ sensor NCS1 and is impaired in Wolfram syndrome» (en anglès). Science Signaling, 11, 553, 23-10-2018, pàg. eaaq1380. DOI: 10.1126/scisignal.aaq1380. ISSN: 1945-0877.
Strom, T. «Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein». Human Molecular Genetics, 7, 13, 01-12-1998, pàg. 2021–2028. DOI: 10.1093/hmg/7.13.2021. ISSN: 1460-2083.
Esteban Bueno, Gema; Ruano García, Mónica; Grandes Velasco, Sonia; Villar Gómez de las Heras, Karina «Una familia con síndrome de Wolfram». Revista Clínica de Medicina de Familia, 6, 1, 2013-2, pàg. 54–57. DOI: 10.4321/S1699-695X2013000100011. ISSN: 1699-695X.
Yamaguchi, Suguru; Ishihara, Hisamitsu; Tamura, Akira; Yamada, Takahiro; Takahashi, Rui «Endoplasmic reticulum stress and N-glycosylation modulate expression of WFS1 protein». Biochemical and Biophysical Research Communications, 325, 1, 03-12-2004, pàg. 250–256. DOI: 10.1016/j.bbrc.2004.10.017. ISSN: 0006-291X. PMID: 15522226.