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5,466 Possible Causes for HSP, binding, coding, strand

Did you mean: HSP, binding, choking, strand

  • Influenza

    In an attempt to get around this, Si et al. expanded the genetic code of influenza A viruses.[] Abstract Human influenza viruses passaged in eggs often acquire mutations in the hemagglutinin (HA) receptor binding site (RBS).[] Structure of the influenza virus Human influenza viruses are single-stranded RNA viruses with a pleomorphic appearance and a diameter range between 80 to 120 nanometers.[] Abstract We reported a 16-year-old boy who developed Henoch-Schönlein purpura (HSP) 15 days after receiving a seasonal influenza vaccine.[]

  • Orchitis

    Specific Code Male Dx N45.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.[] In support, HMGB1 triggered extracellular signal regulated kinase (ERK)1/2 and cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB) activation in[] Epidemiology Mumps orchitis develops in 30% of patients with mumps after puberty Etiology of Mumps Orchitis Mumps virus is a paramyxovirus with a single-stranded RNA.[] Abstract Henoch-Schönlein purpura (HSP) is the most common cause of nonthrombocytopenic purpura in children.[]

  • Classical Swine Fever

    On the basis of the veterinarians' reports, each visit was coded as 0 (negative clinical diagnosis) or 1 (positive clinical diagnosis).[] Using a minilibrary of porcine ISGs, we identify porcine guanylate-binding protein 1 (GBP1) as a potent antiviral ISG against CSFV.[] In this study, we explored the role of CSFV E(rns) in IFN-beta induction by exogenous double-stranded (ds) RNA.[] ISBN This bar-code number lets you verify that you're getting exactly the right version or edition of a book. The 13-digit and 10-digit formats both work.[]

  • Intussusception

    Code K38.8 Other specified diseases of appendix 2016 2017 2018 2019 Billable/Specific Code Applicable To Intussusception of appendix K38.8 ) The following code(s) above K56.1[] BACKGROUND/PURPOSE: Serum Intestinal Fatty-Acid Binding Protein (I-FABP) is a useful marker of bowel necrosis in pediatric intussusception.[] Laboratory analysis showed: thrombocytopaenia, lymphopaenia, positive antinuclear antibody, antidouble-stranded DNA, Coombs tests and low C3 in combination with an active[] The latter condition is seen in people with special medical conditions such as Henoch-Schönlein purpura (HSP), cystic fibrosis and hematologic dyscrasia.[]

  • Cerebellar Ataxia

    Wherever such a combination exists there is a "use additional code" note at the etiology code, and a "code first" note at the manifestation code.[] Hence, in this case, increased C-CB184 binding may reflect persistent microglial activation along with HIV persistence in the cerebellum.[] Abstract XRCC1 is a molecular scaffold protein that assembles multi-protein complexes involved in DNA single-strand break repair.[] Abstract Cerebellar ataxia (CA) and hereditary spastic paraplegia (HSP) are two of the most prevalent motor disorders with extensive locus and allelic heterogeneity.[]

  • Hepatocellular Carcinoma

    Abstract Long non-coding RNAs (lncRNAs) have been demonstrated to be involved in the development and progression of multiple cancers by previous studies.[] Mechanistically, hypoxic stress in the HCC cells promoted YAP binding to HIF-1α in the nucleus and sustained HIF-1α protein stability to bind to PKM2 gene and directly activates[] Percutaneous puncture endovascular placement of iodine-125 (I) seeds strand and stent is reported to treat HCC with tumor thrombus effectively.[] Abstract Although Henoch-Schönlein purpura (HSP) is known to be accompanied by malignancies, cases with hepatobiliary cancer are extremely rare.[]

  • Chilblain

    Codes within the T section that include the external cause do not require an additional external cause code Use Additional code to identify any retained foreign body, if applicable[] Natural organics absorbs and binds cells together strengthening capillaries. It allows cells (capillaries) to move while giving them structure.[] We have recently shown that TREX1 plays a role in apoptotic single-stranded DNA damage induced by the killer lymphocyte protease granzyme A.[] ., immune-mediated Henoch-Schönlein purpura or Churg-Strauss syndrome; leukocytoclastic, urticarial vasculitis; granulomatous vasculitis), embolism or systemic lupus erythematosus[]

  • Toxocara Canis

    The four genes (termed ant-3, -5, -30 and -34), share no coding sequence similarity, although their 3'UTRs (untranslated regions) are homologous.[] A structure was predicted with ligand binding sites predicted at H93, N95, N226, L94, I79, and I210 and with active sites predicted at I256 and G207.[] MATERIALS AND METHODS: The gene that codes for TES-30 was cloned in the expression vector pET28a ( ) using single-stranded oligonucleotides united by PCR.[] Abstract We describe a case of Henoch-Schönlein purpura in the onset of Toxocara canis infection.[]

  • Factor XIII Deficiency

    Congenital FXIII deficiency is an autosomal recessive disorder, usually attributed to a defect in the FXIIIA and B subunits coding, respectively, by F13A and F13B genes.[] Bioinformatic analysis predicts that the insertion of four amino acids affects the site 3 of calcium binding site, which disturbs the smooth function of the FXIIIA peptide[] Mutation analysis was performed on amplified DNA from each exon of this gene by single-strand conformation polymorphism (SSCP) and DNA sequencing techniques.[] We report two consecutive pediatric patients with Henoch-Schönlein purpura (HSP) and symptomatic decrease in FXIII.[]

  • Mental Retardation

    Recent research showed that FMRP participates in non-coding RNA pathways and plays various important roles in physiology, thereby extending our knowledge of the pathogenesis[] Here, we report the identification of a new SUMO-binding protein, ZNF261.[] Downregulation of Drosophila Torsin (DTor) by DTor-specific inhibitory double-stranded RNA (RNAi) induced abnormal locomotor behavior and increased susceptibility to H2O2.[] By exome sequencing, we detected compound-heterozygous mutations in PIGO, a gene coding for a membrane protein of the same molecular pathway, in two siblings with HPMRS, and[]