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4,264 Possible Causes for C(gamma), cAMP dependent, kinase, protein

Did you mean: C(gamma), cAMP, dependent, kinase, protein

  • Influenza

    There was virtually no response or acknowledgment to the epidemics in March and April in the military camps.[virus.stanford.edu] C., W. Allan, M. Eichelberger, and S. R. Carding. 1992 . Roles of alpha beta and gamma delta T cell subsets in viral immunity. Annu. Rev. Immunol. 10 : 123 -151.[dx.doi.org] Eventually, the diagnosis of anti-single recognition particle-mediated necrotizing myopathy was made based on elevated creatine kinase, thigh magnetic resonance imaging, muscle[ncbi.nlm.nih.gov] Influenza virus M2 protein is an integral membrane protein expressed on the infected-cell surface. Cell 40 , 627–633 (1985). 5. Zebedee, S.L. & Lamb, R.A.[dx.doi.org]

  • Spinocerebellar Ataxia Type 14

    Recently, a mutation in the protein kinase C gamma gene (PRKCG) was identified in a US family of English and Dutch ancestry with autosomal dominant SCA whose disease mapped[ncbi.nlm.nih.gov] Abstract Spinocerebellar ataxia type 14 (SCA14) is an autosomal dominant neurodegenerative disease caused by mutations in protein kinase Cgamma (PKCgamma).[ncbi.nlm.nih.gov] Aggregation of misfolded proteins is generally involved in the pathogenesis of many neurodegenerative diseases.[ncbi.nlm.nih.gov] […] of the catalytic domain of protein kinase C gamma.[ncbi.nlm.nih.gov]

    Missing: cAMP dependent
  • Carney Complex

    Epac1-camps.[ncbi.nlm.nih.gov] Its central component is the protein kinase A (PKA).[ncbi.nlm.nih.gov] The PRKAR1A gene encodes the type 1A regulatory subunit of cAMP-dependent protein kinase A.[ncbi.nlm.nih.gov] […] primarily by spotty skin pigmentation and a variety of endocrine and other tumors, is caused by mutations in PRKAR1A, the gene that codes for the RIalpha subunit of protein kinase[ncbi.nlm.nih.gov]

    Missing: C(gamma)
  • Ataxia Telangiectasia

    Nuclear HDAC4 binds to chromatin, as well as to myocyte enhancer factor 2A (MEF2A) and cAMP-responsive element binding protein (CREB), leading to histone deacetylation and[ncbi.nlm.nih.gov] […] and gamma radiation: an evaluation of ligating activities involved in different DNA repair processes .[doi.org] Compound 27g was also significantly more selective against other kinases than 4.[ncbi.nlm.nih.gov] Here we identified that Cpn10/HSPE, a 10-kDa heat shock protein, is a novel interacting partner of NPAT.[ncbi.nlm.nih.gov]

  • Neurodegeneration with Brain Iron Accumulation

    In 2006, he was an average boy, able to hike and camp, but by December 2008, his parents had to bring Travis to his first appointment at Children’s Hospital in a wagon.[childrenshospitaloakland.org] […] acid ( GABA ) A receptor, gamma 2 ( GABRG2 ); Epilessia mioclonica giovanile di Janz : geni EF-hand domain ( C-terminal ) containing 1 ( EFHC1 ); Epilessia mioclonica severa[isn.cnr.it] Four patients were found to have mutations in the pantothenate kinase 2 (PANK2) gene.[ncbi.nlm.nih.gov] Because of the mitochondrial localization of the derived protein, this variant is referred to as mitochondrial membrane protein-associated neurodegeneration with brain iron[ncbi.nlm.nih.gov]

  • Urinary Tract Infection

    Forskolin A plant extract and adenylyl cyclase activator with a potent capacity to increase intracellular cAMP levels.[doi.org] Interleukin-17 Kidney/microbiology Mice Mice, Inbred BALB C Proteus mirabilis/genetics Proteus mirabilis/immunology* Recombinant Proteins/immunology* Spleen Urinary Bladder[ncbi.nlm.nih.gov] E. coli activates TLR4, which is responsible for the activation of IL-12, extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK).[ncbi.nlm.nih.gov] E. coli activates TLR4, which is responsible for the activation of IL-12, extracellular signal–regulated kinase (ERK) and c-Jun N-terminal kinase (JNK).[doi.org]

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    Type VIII (Liver phosphorylase kinase deficiency) Type IX (Liver and muscle phosphorylase kinase deficiency) Type X (cAMP dependent protein kinase A deficiency) There is hepatomegaly[edusanjalbiochemist.blogspot.com] Journal N Engl J Med 362:1203-10 (2010) DOI: 10.1056/NEJMoa0900661 Reference PMID: 15877279 (GSD of Heart) Authors Burwinkel B, Scott JW, Buhrer C, van Landeghem FK, Cox GF[genome.jp] […] such as protein kinase A (PKA, cAMP-dependent kinase).[en.wikipedia.org] Nat Genet. 1996; 14 :337–40. [ PubMed : 8896567 ] Maire I, Baussan C, Moatti N, Mathieu M, Lemonnier A.[ncbi.nlm.nih.gov]

  • PDE4D Haploinsufficiency Syndrome

    PRKAR1A 65 Annotation score: K7EMZ6 K7EMZ6_HUMAN cAMP-dependent protein kinase type ...[uniprot.org] […] zeta Antibodies anti-Protein Kinase C, theta Antibodies anti-Protein Kinase C, iota Antibodies anti-Protein Kinase C, gamma Antibodies anti-Protein Kinase, CAMP-Dependent[antibodies-online.com] Identified in a complex composed of RYR1, PDE4D, PKA, FKBP1A and protein phosphatase 1 (PP1) (By similarity).[genecards.org] […] deficiency Limb-girdle muscular dystrophy due to lamin A/C deficiency Limb-girdle muscular dystrophy due to myotilin deficiency Limb-girdle muscular dystrophy due to TRIM32[csbg.cnb.csic.es]

  • Phosphorylase Kinase Deficiency

    […] activates cAMP-dependent protein kinase 2. cAMP-dependent protein kinase phosphorylates phosphorylase kinase a 3 Phosphorylase kinase a phosphorylates glycogen synthase a[quizlet.com] Nat Genet. 1996; 14 :337–40. [ PubMed : 8896567 ] Maire I, Baussan C, Moatti N, Mathieu M, Lemonnier A.[ncbi.nlm.nih.gov] There are several types of PKD, stemming from the deficiency of either liver phosphorylase kinase, muscle phosphorylase kinase, or both.[symptoma.com] The report of a pathogenic mutation (R531Q) in the gene (PRKAG2) encoding the gamma2 subunit of AMP-activated protein kinase (AMPK) in three infants with congenital hypertrophic[ncbi.nlm.nih.gov]

  • Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency

    Patients with a defect of the cAMP-dependent protein kinase have been infrequently reported.[checkorphan.org] Journal N Engl J Med 362:1203-10 (2010) DOI: 10.1056/NEJMoa0900661 Reference PMID: 15877279 (GSD of Heart) Authors Burwinkel B, Scott JW, Buhrer C, van Landeghem FK, Cox GF[genome.jp] Diagnostic methods Biochemical diagnosis is made by measuring phosphorylase kinase activity in blood cells or in a liver biopsy.[orpha.net] ITPR1 isoform 1 is a 2710 amino acid protein, isoform 2 is a 2695 amino acid protein, and isoform 3 is a 2743 amino acid protein.[themedicalbiochemistrypage.org]

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