ITPR1 (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ITPR1" in Portuguese language version.

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Nucifora FC Jr, Li SH, Danoff S, Ullrich A, Ross CA (1996). «Molecular cloning of a cDNA for the human inositol 1,4,5-trisphosphate receptor type 1, and the identification of a third alternatively spliced variant». Brain Res Mol Brain Res. 32 (2): 291–6. PMID 7500840. doi:10.1016/0169-328X(95)00089-B
van de Leemput J, Chandran J, Knight MA, Holtzclaw LA, Scholz S, Cookson MR, Houlden H, Gwinn-Hardy K, Fung HC, Lin X, Hernandez D, Simon-Sanchez J, Wood NW, Giunti P, Rafferty I, Hardy J, Storey E, Gardner RJ, Forrest SM, Fisher EM, Russell JT, Cai H, Singleton AB (2007). «Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans». PLoS Genet. 3 (6): e108. PMC 1892049. PMID 17590087. doi:10.1371/journal.pgen.0030108
Iwaki A, Kawano Y, Miura S, Shibata H, Matsuse D, Li W, Furuya H, Ohyagi Y, Taniwaki T, Kira J, Fukumaki Y (2008). «Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16». J Med Genet. 45 (1): 32–5. PMID 17932120. doi:10.1136/jmg.2007.053942

Yamada N, Makino Y, Clark RA, Pearson DW, Mattei MG, Guenet JL, Ohama E, Fujino I, Miyawaki A, Furuichi T; et al. (1994). «Human inositol 1,4,5-trisphosphate type-1 receptor, InsP3R1: structure, function, regulation of expression and chromosomal localization». Biochem J. 302 ( Pt 3): 781–90. PMC 1137299. PMID 7945203
Nucifora FC Jr, Li SH, Danoff S, Ullrich A, Ross CA (1996). «Molecular cloning of a cDNA for the human inositol 1,4,5-trisphosphate receptor type 1, and the identification of a third alternatively spliced variant». Brain Res Mol Brain Res. 32 (2): 291–6. PMID 7500840. doi:10.1016/0169-328X(95)00089-B
van de Leemput J, Chandran J, Knight MA, Holtzclaw LA, Scholz S, Cookson MR, Houlden H, Gwinn-Hardy K, Fung HC, Lin X, Hernandez D, Simon-Sanchez J, Wood NW, Giunti P, Rafferty I, Hardy J, Storey E, Gardner RJ, Forrest SM, Fisher EM, Russell JT, Cai H, Singleton AB (2007). «Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans». PLoS Genet. 3 (6): e108. PMC 1892049. PMID 17590087. doi:10.1371/journal.pgen.0030108
Iwaki A, Kawano Y, Miura S, Shibata H, Matsuse D, Li W, Furuya H, Ohyagi Y, Taniwaki T, Kira J, Fukumaki Y (2008). «Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16». J Med Genet. 45 (1): 32–5. PMID 17932120. doi:10.1136/jmg.2007.053942
«Entrez Gene: ITPR1 inositol 1,4,5-triphosphate receptor, type 1»