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20 Possible Causes for catabolism, snoRNA

Did you mean: catabolism, snoring

  • Growth Retardation

    Autophagy is an intracellular catabolic process of lysosome-dependent recycling of intracellular organelles and protein complexes.[] The PWS-critical region (PWScr) contains an array of non-protein coding IPW-A exons hosting intronic SNORD116 snoRNA genes.[] . • Hematologic - hyperviscosity and polycythemia due to increase erythropoietin level sec. to hypoxia • Immunologic - IUGR have increased protein catabolism and decreased[]

  • Shigella Flexneri

    Transcript profiling and cell culture assays using glpD and glpK mutants showed that enhancement of glycerol catabolism were related with adhesion ability of S. flexneri.[] PubMed View Article Google Scholar Schattner P, Brooks AN, Lowe TM: The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs.[]

  • Plasmodium

    […] glucocorticoids and mineralocorticoids, bile acid metabolism (alternative pathway), sulfur metabolism, bile acid metabolism, metabolism of estrogens and androgens, cholesterol catabolism[] RBPs also play crucial roles in processing of stable RNAs such as rRNA, tRNA, snRNA, and snoRNA [ 14 ].[] Maturation of 40S and 60S ribosomal subunits PF3D7_0504400 DDX21 PfDdx21p RNA processing and nucleolar localization PF3D7_1217200 Mrd1p PfMrd1p Release of base-paired U3 snoRNA[]

  • Saccharomyces Cerevisiae

    Also, metabolic engineering efforts to alter sucrose catabolism are presented in a chronological manner.[] […] known to encode 25S, 18S, 5.8S and 5S rRNAs, six snRNAs, 67 snoRNAs, five stable RNAs and 299 tRNAs.[] The mean concentration of total nitrogen utilized during the catabolism of 1.11 M (200 g/L) glucose when all amino acids were in excess was 400 mg N/L with a range of 140[]

  • Carbamoyl Phosphate Synthetase Deficiency

    Overview Defects in specific amino acid catabolism Hartnup's disease deficiency of neutral amino acid transporter leads to tryptophan absorption presentation pellagra result[] Zellkern Fu: Baustein Ribosom ( 60% des Ribosoms) sn Small nuklear Struktur: Einzelstrang Vorkommen: Zellkern Fu: Bildung von Komplexen mit Proteinen zum Splicing der hnRNA snoRNA[] […] disease dominated by severe hyperammonemia in neonates or as a more insidious late-onset condition, generally manifesting as life-threatening hyperammonemic crises under catabolic[]

  • Hoyeraal-Hreidarsson Syndrome

    For more than three decades he worked on different areas of biology including thymineless death in bacteria, genetic control of nucleotide catabolism, development of anti‐AIDS[] […] was linked to mutations in DKC1 , which encodes the highly conserved multifunctional protein dyskerin. 2 – 7 Dyskerin associates with a subclass of small nucleolar RNAs (snoRNAs[] […] encodes for Dyskerin, a 514 aminoacid protein Expression widespread tissue repartition Function Dyskerin is the nucleolar pseudouridine synthetase component of the box H ACA snoRNAs[]

  • Hypogonadotropic Hypogonadism - Retinitis pigmentosa Syndrome

    Adrenal failure is an almost constant finding in X-ALD and is caused by defective catabolism resulting in VLCFA accumulation, which interferes with steroid hormone synthesis[] […] by deficiency of one or more paternally expressed imprinted transcripts within chromosome 15q11-q13, a region that includes SNURF-SNRPN and multiple small nucleolar RNAs (snoRNAs[] […] in a child with PWS provides strong evidence that deficiency of HBII-85 snoRNAs plays a major role in the key characteristics of the PWS phenotype. 6 However, some atypical[]

  • Pontocerebellar Hypoplasia Type 1B

    […] exonucleolytic trimming to generate mature 3'-end of 5.8S rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA); DNA deamination; rRNA processing; mRNA catabolic[] In the nucleus, the RNA exosome complex is involved in proper maturation of stable RNA species such as rRNA, snRNA and snoRNA, in the elimination of RNA processing by-products[]

  • Retinitis Pigmentosa 11

    Morita M, Oike Y, Nagashima T, Kadomatsu T, Tabata M, et al. (2011) Obesity resistance and increased hepatic expression of catabolism-related mRNAs in Cnot3 / mice.[] U4 snRNP U4 snRNP U4atac snRNP U4atac snRNP Cajal body nuclear speck U4 snRNA binding U4atac snRNA binding ribonucleoprotein complex binding U4/U6 x U5 tri-snRNP complex snoRNA[]

  • 14q11-q22 Microdeletion Syndrome

    […] mitochondrial disorders HIBCH (3‐hydroxyisobutyryl‐CoA hydrolase) deficiency (MIM #250620) is a rare autosomal recessive inborn error of metabolism, leading to a block in the catabolic[] BMP4 14q22.2 Loss hypoplasia, anophthalmia, brain/digital anomalies 176270 Prader-Willi syndrome (PWS) PWS-SRO, SNRPN, 15q11.2-q12 Loss 105830 Angelman syndrome (AS) 608636 snoRNAs[]

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