HSPB8
HSPB8 (Heat shock protein family B (small) member 8) هوَ بروتين يُشَفر بواسطة جين HSPB8 في الإنسان.[1][2][3]
الوظيفة
المراجع
- "Effects of estrogen on global gene expression: identification of novel targets of estrogen action"، Cancer Res، 60 (21): 5977–83، نوفمبر 2000، PMID 11085516.
- "A novel human gene similar to the protein kinase (PK) coding domain of the large subunit of herpes simplex virus type 2 ribonucleotide reductase (ICP10) codes for a serine-threonine PK and is expressed in melanoma cells"، J Biol Chem، 275 (33): 25690–9، سبتمبر 2000، doi:10.1074/jbc.M002140200، PMID 10833516.
- "Entrez Gene: HSPB8 Heat shock 22kDa protein 8"، مؤرشف من الأصل في 05 ديسمبر 2010.
قراءة متعمقة
- "Structure, function, property, and role in neurologic diseases and other diseases of the sHsp22"، J. Neurosci. Res.، 85 (10): 2071–9، 2007، doi:10.1002/jnr.21231، PMID 17304582.
- "Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree"، J. Neurol. Sci.، 109 (1): 41–8، 1992، doi:10.1016/0022-510X(92)90091-X، PMID 1517763.
- "Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family"، Brain، 109 ( Pt 5) (5): 897–914، 1986، doi:10.1093/brain/109.5.897، PMID 3022865.
- "A rapidly progressive autosomal dominant scapulohumeral form of spinal muscular atrophy"، Ann. Neurol.، 20 (4): 538–40، 1986، doi:10.1002/ana.410200417، PMID 3789668.
- "A distal form of chronic spinal muscular atrophy"، Neurology، 19 (1): 53–8، 1969، doi:10.1212/wnl.19.1.53، PMID 5813127.
- "Benign familial spinal muscular atrophy with hypertrophy of the calves"، Arch. Neurol.، 39 (10): 657–60، 1982، doi:10.1001/archneur.1982.00510220055013، PMID 7125978.
- "Dominant inherited distal spinal muscular atrophy with atrophic and hypertrophic calves"، J. Neurol. Sci.، 114 (1): 81–4، 1993، doi:10.1016/0022-510X(93)90053-2، PMID 8433103.
- "Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24"، Hum. Mol. Genet.، 5 (7): 1065–9، 1997، doi:10.1093/hmg/5.7.1065، PMID 8817349.
- "A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene"، Genomics، 65 (1): 34–43، 2000، doi:10.1006/geno.2000.6149، PMID 10777663.
- "A novel gene expressed in human keratinocytes with long-term in vitro growth potential is required for cell growth"، J. Invest. Dermatol.، 116 (2): 286–95، 2001، doi:10.1046/j.1523-1747.2001.00191.x، PMID 11180006.
- "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs"، Genome Res.، 11 (3): 422–35، 2001، doi:10.1101/gr.GR1547R، PMC 311072، PMID 11230166.
- "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing"، EMBO Rep.، 1 (3): 287–92، 2001، doi:10.1093/embo-reports/kvd058، PMC 1083732، PMID 11256614.
- "Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells"، Int. J. Oncol.، 18 (5): 905–11، 2001، doi:10.3892/ijo.18.5.905، PMID 11295034.
- "HSP22, a new member of the small heat shock protein superfamily, interacts with mimic of phosphorylated HSP27 ((3D)HSP27)"، J. Biol. Chem.، 276 (29): 26753–61، 2001، doi:10.1074/jbc.M103001200، PMID 11342557.
- "Characterization of two novel human small heat shock proteins: protein kinase-related HspB8 and testis-specific HspB9"، Biochim. Biophys. Acta، 1520 (1): 1–6، 2001، doi:10.1016/s0167-4781(01)00237-8، PMID 11470154.
- "Protein–Protein Interaction Panel Using Mouse Full-Length cDNAs"، Genome Res.، 11 (10): 1758–65، 2001، doi:10.1101/gr.180101، PMC 311163، PMID 11591653.
- "Phosphopeptide derivatization signatures to identify serine and threonine phosphorylated peptides by mass spectrometry"، Anal. Chem.، 73 (22): 5387–94، 2002، doi:10.1021/ac0104227، PMID 11816564.
- "H11 kinase is a novel mediator of myocardial hypertrophy in vivo"، Circ. Res.، 91 (11): 1007–14، 2002، doi:10.1161/01.RES.0000044380.54893.4B، PMID 12456486.
بوابة طب
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
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