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Calsenilin Enhances Apoptosis by Altering Endoplasmic Reticulum Calcium Signaling

Autor: Lilliehook, C., Chan, S., Choi, E.K., Zaidi, N.F., Wasco, W., Mattson, M.P., Buxbaum, J.D. ^{11To whom correspondence should be addressed at the Department of Psychiatry, Box 1230, Mount Sinai Medical Center, One Gustave L. Levy Place, New York, NY 10029. Fax: (212) 828-4221. E-mail: buxbaj01@doc.mssm.edu.}

Publikováno v: In Molecular and Cellular Neuroscience April 2002 19(4):552-559

Targeting mitochondrial metabolism with CPI-613 in chemoresistant ovarian tumors.

Autor: Udumula, Mary P.^1,2,3 (AUTHOR), Rashid, Faraz⁴ (AUTHOR), Singh, Harshit^1,2 (AUTHOR), Pardee, Tim⁵ (AUTHOR), Luther, Sanjeev⁶ (AUTHOR), Bhardwaj, Tanya^1,7 (AUTHOR), Anjaly, Km^1,2 (AUTHOR), Piloni, Sofia^1,2 (AUTHOR), Hijaz, Miriana^1,2,3 (AUTHOR), Gogoi, Radhika⁸ (AUTHOR), Philip, Philip A.^2,9 (AUTHOR), Munkarah, Adnan R.^1,2 (AUTHOR), Giri, Shailendra⁴ (AUTHOR), Rattan, Ramandeep^1,2,3,8 (AUTHOR) rrattan1@hfhs.org

Publikováno v: Journal of Ovarian Research. 11/14/2024, Vol. 17 Issue 1, p1-17. 17p.

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

Autor: Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R. E., Chernov, I., Devoto, Marcella, Brzustowicz, L. M., Cayanis, E., Vitale, E., Russo, J. J., Matseoane, D., Boukhgalter, B., Wasco, W., Figus, A. L., Loudianos, J., Cao, A., Sternlieb, I., Evgrafov, G., Parano, E., Pavone, L., Warburton, D., Ott, J., Penchaszadeh, G. K., Scheinberg, I. H., Gilliam, T. C.

Publikováno v: Nature genetics
5 (1993): 338–343. doi:10.1038/ng1293-338
info:cnr-pdr/source/autori:Petrukhin K.; Fischer S.G.; Pirastu M.; Tanzi R.E.; Chernov I.; Devoto M.; Brzustowicz L.M.; Cayanis E.; Vitale E.; Russo J.J.; Matseoane D.; Boukhgalter B.; Wasco W.; Figus A.L.; Loudianos J.; Cao A.; Sternlieb I.; Evgrafov O.; Parano E./titolo:Mapping, cloning and genetic characterization of the region containing the Wilson disease gene/doi:10.1038%2Fng1293-338/rivista:Nature genetics (Print)/anno:1993/pagina_da:338/pagina_a:343/intervallo_pagine:338–343/volume:5

Wilson disease (WD) is an autosomal recessive disorder of copper transport which maps to chromosome 13q14.3. In pursuit of the WD gene, we developed yeast artificial chromosome and cosmid contigs, and microsatellite markers which span the WD gene reg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bb9b3e7f527bd0994117a01c1df6b1e
https://doi.org/10.1038/ng1293-338

A familial Alzheimer's disease associated mutation in presenilin-1 mediates amyloid-beta independent cell specific neurodegeneration.

Autor: Parvand, Mahraz¹ (AUTHOR), Liang, Joseph J. H.¹ (AUTHOR), Bozorgmehr, Tahereh¹ (AUTHOR), Born, Dawson¹ (AUTHOR), Luna Cortes, Alvaro¹ (AUTHOR), Rankin, Catharine H.^1,2 (AUTHOR) crankin@psych.ubc.ca

Publikováno v: PLoS ONE. 9/6/2024, Vol. 19 Issue 9, p1-24. 24p.