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11 Possible Causes for HSP25, kinase

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  • Cardiac Hypertrophy

    In addition, MAPKAPK2 and 3 phosphorylate Hsp25/27 and may thereby confer cytoprotection.[qiagen.com] Myosin light chain kinase (MLCK), a specific kinase for the phosphorylation of myosin light chain 2 (MLC2), plays an important role in regulating cardiac muscle contraction[ncbi.nlm.nih.gov] Mechanistically, our study suggests that TRIM8 may elicit cardiodetrimental effects by promoting the activation of transforming growth factor β-activated kinase 1 (TAK1)-p38[ncbi.nlm.nih.gov]

  • Distal Hereditary Motor Neuropathy

    […] berardinelli-seip congenital lipodystrophy 2 (seipin) gng3lg, mouse, homolog of BSCL2 606158 15832 heat shock protein family B (small) member 1 heat shock 27kDa protein 1 HSPB1 HS.76067 HSP25[ukgtn.nhs.uk] […] distal HMN II region: the cytoskeletal proteins paxillin (PXN) and restin (RSN); the acidic ribosomal phosphoprotein, large P0 subunit (RPLP0); a nucleoside diphosphate kinase[ncbi.nlm.nih.gov] The clinical features, moderately raised creatin kinase levels, selective pattern of muscle involvement on magnetic resonance imaging and pathological changes on muscle biopsy[readbyqxmd.com]

  • Distal Hereditary Motor Neuropathy Type 1

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] […] distal HMN II region: the cytoskeletal proteins paxillin ( PXN ) and restin ( RSN ); the acidic ribosomal phosphoprotein, large P0 subunit ( RPLP0 ); a nucleoside diphosphate kinase[cambridge.org] […] syndrome Giant axonal neuropathy Global developmental delay-osteopenia-ectodermal defect syndrome Glomuvenous malformation Glutaryl-CoA dehydrogenase deficiency Glycerol kinase[se-atlas.de]

  • Distal Hereditary Motor Neuropathy Type 7

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] Creatine kinase will be elevated. [2] Congenital Myopathies They may present at birth with marked weakness, hypotonia, external ophthalmoplegia and respiratory failure.[explainmedicine.com] […] repeat amplification products, which were transferred to nylon membranes, with [γ- 32 P]dATP (Amersham, UK) end-labelled oligonucleotide primers using T4 polynucleotide DNA kinase[academic.oup.com]

  • Distal Hereditary Motor Neuropathy Type 7A

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] Creatine kinase will be elevated. [2] Congenital Myopathies They may present at birth with marked weakness, hypotonia, external ophthalmoplegia and respiratory failure.[explainmedicine.com] Creatine kinase. Serum and urine protein electrophoresis. Muscle biopsy. Cerebrospinal fluid (CSF) examination. MRI of the brain and spinal cord.[patient.info]

  • Distal Hereditary Motor Neuropathy Type 2A

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] Creatine kinase will be elevated. [2] Congenital Myopathies They may present at birth with marked weakness, hypotonia, external ophthalmoplegia and respiratory failure.[explainmedicine.com] […] berardinelli-seip congenital lipodystrophy 2 (seipin) gng3lg, mouse, homolog of BSCL2 606158 15832 heat shock protein family B (small) member 1 heat shock 27kDa protein 1 HSPB1 HS.76067 HSP25[ukgtn.nhs.uk]

  • Distal Hereditary Motor Neuropathy Type 2C

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] […] neuronally neuronally neuronally Neuronally Expressed EPH-Related Tyrosine Kinase Neuronally-expressed EPH-related tyrosine kinase Neuronavigation neurone neurone neurone[medical-dictionary.thefreedictionary.com] PMID 19132982 Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle.[atlasgeneticsoncology.org]

  • Distal Hereditary Motor Neuropathy Type 2

    Members of the HspB family Name Synonyms Uniprot ID Chromosome Location Number of amino acid residues HspB1 Hsp25, Hsp27,Hsp28 P04792 7q11.23 205 HspB2 MKBP Q16082 11q22-q23[hsp27.com] Creatine kinase will be elevated. [2] Congenital Myopathies They may present at birth with marked weakness, hypotonia, external ophthalmoplegia and respiratory failure.[explainmedicine.com] PMID 19132982 Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle.[atlasgeneticsoncology.org]

  • Mycobacterium Leprae

    The C-terminal domain varies from 12 residues in human hsp20 to 36 residues in mouse hsp25. The N-terminal extension is highly variable among different sHsps.[bmcmicrobiol.biomedcentral.com] Apart from the most central MTB protein, which belongs to the PE family, the most central proteins in MSM and MLP (and its orthologs) are Serinethreonine protein kinases.[omicsonline.org] Similarly in SCs, M. leprae infection is related to modulation of host kinases [ 136 ].[ncbi.nlm.nih.gov]

  • Distal Hereditary Motor Neuropathy Type 5

    PMID 19132982 Comparison of the small heat shock proteins alphaB-crystallin, MKBP, HSP25, HSP20, and cvHSP in heart and skeletal muscle.[atlasgeneticsoncology.org] Creatine kinase will be elevated. [2] Congenital Myopathies They may present at birth with marked weakness, hypotonia, external ophthalmoplegia and respiratory failure.[explainmedicine.com] Creatine kinase. Serum and urine protein electrophoresis. Muscle biopsy. Cerebrospinal fluid (CSF) examination. MRI of the brain and spinal cord.[patient.info]

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