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793 Possible Causes for Gallus, TEF 1, Divergent, gallus, protein

Did you mean: Gallus, TEF, 1, Divergent, gallus, protein

  • Werner Syndrome

    Cerebrotendinous Xanthomatosis Antonio Federico, Maria Teresa Dotti, and Gian Nicola Gallus. Initial Posting: July 16, 2003; Last Update: April 14, 2016.[ncbi.nlm.nih.gov] Plenum, New York, pp 215–218 Google Scholar Suzuki T, Shiratori M, Furuichi Y, Matsumoto T (2001) Diverged nuclear localization of Werner helicase in human and mouse cells[link.springer.com] Here we report that the WS protein does indeed catalyze DNA unwinding.[ncbi.nlm.nih.gov] Table 2 Hww syndrome: mr findings Uterus didelphys It is characterized by two symmetric, widely divergent uterine horns and two cervixes, with an enlarged cavity filled by[bmcmedimaging.biomedcentral.com] […] helicases, genomic instability, and human genetic disease ANNUAL-REVIEW-OF-GENOMICS-AND-HUMAN-GENETICS. 2000; 1 : 409-459 Suzuki,-T; Shiratori,-M; Furuichi,-Y; Matsumoto,-T Diverged[malattierare.regione.veneto.it]

  • Bloom Syndrome

    Jing Shi, Na-Nv Liu, Yan-Tao Yang and Xu-Guang Xi , Purification and enzymatic characterization of Gallus gallus BLM helicase , The Journal of Biochemistry , 162 , 3 , (183[doi.org] BLM, the protein altered in BS, is a member of the RecQ DNA helicase family, whose members share an average of 40% identity in the helicase domain and have divergent N-terminal[ncbi.nlm.nih.gov] Only single examples of a tracheoesophageal fistula, a cardiac malformation, absence/malformation of the thumbs, and absence of a toe have been reported in the Bloom registry[clinicaladvisor.com] PRKAR1A and other protein kinase A (PKA) subunits were expressed in Bloom syndrome cells and their level of expression differed by subunit and cell type.[ncbi.nlm.nih.gov] Cerebrotendinous Xanthomatosis Antonio Federico, Maria Teresa Dotti, and Gian Nicola Gallus. Initial Posting: July 16, 2003; Last Update: April 14, 2016.[ncbi.nlm.nih.gov]

  • Neuronal Ceroid Lipofuscinosis

    The human (Homo sapiens) CSPα protein sequence (Q9H3Z4) was compared to Mus musculus, Bos taurus, Rattus norvegicus, Gallus gallus, Xenopus (Silurana) tropicalis and Canis[journals.plos.org] The NCLs exemplify both phenotypic convergence and divergence, and there can be very wide disease severity caused by mutations in the same gene.[els.net] fistula type 1 Microcephaly - intracranial calcification - intellectual deficit Microcephaly - lymphedema - chorioretinopathy Microcephaly - microphthalmia - ectrodactyly[csbg.cnb.csic.es] To gain insight into the function of CLN8 protein, we employed the split-ubiquitin membrane-based yeast two-hybrid (MYTH) system, which detects protein-protein interactions[ncbi.nlm.nih.gov] We expressed a novel 33 kDa protein that is highly similar to CLN3P.[ncbi.nlm.nih.gov]

  • Sunburn

    Naldi L, Altieri A, Imberti GL, Giordano L, Gallus S, La Vecchia C. Cutaneous malignant melanoma in women.[ncbi.nlm.nih.gov] Tumor biology of skin cancer is diverging: severe blistering sunburns corresponding to intermittent intense UV exposures are associated with an increased risk for both melanoma[doi.org] One consequence of this is the synthesis of different proteins and enzymes.[scientificamerican.com] […] to expression of erythema (4 h, p 0.001), neutrophil infiltration (24 h, p 0.01), epidermal COX-2 (24 h, p 0.05) and 12-LOX (24 h, p 0.01), and dermal eNOS (24 h, p 0.05) proteins[ncbi.nlm.nih.gov] It is the gene for insulin-like growth factor binding protein-3, (IGFBP3), which modulates the effects of insulin-like growth factor on cells.[doi.org]

    Missing: TEF 1
  • Malignant Neoplasm

    Silvano Gallus, Roberto Foschi, Renato Talamini, Andrea Altieri, Eva Negri, Silvia Franceschi, Maurizio Montella, Luigino Dal Maso, Valerio Ramazzotti and Carlo La Vecchia[doi.org] Opinions have ranged from a conservative attitude to one of removing all goiters containing nodules, whether single or multiple. 1 , 2 In the presence of these divergent opinions[nejm.org] […] of the Hmga1 protein and the Brca1 gene.[doi.org] Moreover, tumors collected from 40 dogs in 5 continents are derived from a single neoplastic clone that has diverged into two subclades.[ncbi.nlm.nih.gov] Fernandez E, Gallus S, La Vecchia C, Talamini E, Negri E, Franceschi S. Family history and environmental risk factors.[doi.org]

    Missing: TEF 1
  • Complement Deficiency Syndrome

    (CF26) 70 lei IgE specific carne de prepelita (CRF192) 70 lei IgE specific carne de pui (Gallus spp.) (CF83) 70 lei IgE specific carne de vaca (Bos spp.)[as-medica.ro] The older studies offer divergent results regarding the association between JIA and null alleles at the C4A and C4B locus [ 13 , 14 ].[link.springer.com] Congenital: Cysts and sinus tracts, tracheoesophageal fistula, abnormal ciliary function. . . . . .[hawaii.edu] Complement Protein H Deficiency is an immunological disorder caused by a deficiency of Factor H , a protein that prevents the immune system from attacking a person's own cells[house.wikia.com] Complement resistance of human carcinoma cells depends on membrane regulatory proteins, protein kinases and sialic acid . Clin. Exp. Immunol. 131 , 254–263 (2003). 98.[nature.com]

  • Juvenile Polyposis Syndrome

    Cerebrotendinous Xanthomatosis Antonio Federico, Maria Teresa Dotti, and Gian Nicola Gallus. Initial Posting: July 16, 2003; Last Update: April 14, 2016.[ncbi.nlm.nih.gov] Key points Hamartomatous polyposis syndromes are inherited autosomal-dominant syndromes that confer predisposition to cancers and have divergent clinical features, but often[nature.com] Abstract Bone morphogenetic proteins regulate many developmental processes during embryogenesis as well as tissue homeostasis in the adult.[ncbi.nlm.nih.gov] , human Bone Morphogenetic Protein Receptors, Type I PTEN Phosphohydrolase PTEN protein, human Supplementary concept Juvenile polyposis syndrome Grant support P30 CA014520[ncbi.nlm.nih.gov] The SMAD 4 gene is responsible for synthesizing the SMAD 4 protein. A group of SMAD proteins bind other proteins to form a complex.[news-medical.net]

  • Familial Congenital Mirror Movements 2

    gallus (chicken) RAD51 NP_990504.1 Danio rerio (zebrafish) rad51 NP_998371.2 Schizosaccharomyces pombe (fission yeast) rhp51 NP_593882.1 LOC708579 XP_001097058.1 Canis lupus[genscript.com] In a cladogram tree based on this alignment, tardigrades tend to cluster together suggesting that they have selective differences in these genes that make them diverge between[jlimnol.it] fistula syndrome Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1 Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type[orpha.net] Multiple protein interactions have been demonstrated for the mammalian Rad51 protein.[mskcc.org] In addition, a 2.5-kb fragment containing a complete HSV-1 tk gene, which is more than 1% divergent compared with that in the tk-neo fusion gene (0.8% and 1.5% divergent in[bloodjournal.org]

  • NADH Cytochrome B5 Reductase Deficiency

    gallus) Aves CYB5R3 6 cytochrome b5 reductase 3 72 (a) 1 1 1(68448251-68462610) lizard (Anolis carolinensis) Reptilia CYB5R3 6 cytochrome b5 reductase 3 73 (a) 1 1 5(91545172[genecards.weizmann.ac.il] […] the estimated divergence times.[journals.plos.org] Ordinary tracheoesophageal fistula (189960) shows little familial aggregation.[findzebra.com] Genome Res. 2004 Oct;14(10B):2121-7. [ PubMed:15489334 ] Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M: Lysine acetylation targets protein[hmdb.ca] Protein Products: Browse Purified and Recombinant Proteins at EMD Millipore Browse R&D Systems for human recombinant proteins Browse recombinant and purified proteins available[genecards.weizmann.ac.il]

  • Polyploidy

    […] paleopolyploidy in model plant species inferred from age distributions of duplicate genes , Plant Cell , 2004 , vol. 16 (pg. 1667 - 1678 ) Chromosome abnormalities in chicken ( Gallus[jhered.oxfordjournals.org] If we combine the results from the two indicators of functional divergence (i.e., expression divergence and asymmetrical sequence divergence), 62% of the recent duplicate[plantcell.org] […] had different intracellular levels of Aurora A, Aurora B, p21, E2F-1, and pRb, suggesting a BRCA2-mediated suppression of polyploidy via stabilization of the checkpoint proteins[ncbi.nlm.nih.gov] This is possibly due to the interaction of TAp73alpha with kinetochore-related proteins leading to the alteration of mitotic checkpoint abilities.[ncbi.nlm.nih.gov] […] eukaryotic proteins than to bacterial proteins.[doi.org]

    Missing: TEF 1

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