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8,506 Possible Causes for (Nonhistone, 2, Chromosomal), Gene, Group, High Mobility, Protein

Did you mean: (Nonhistone, 2, Chromosomal), Gene, gout, High Mobility, proteus

  • Myelodysplasia

    READ MORE I know this is a group for MDS but there is no MDS/MPN group. I was hoping someone here had info. He was diagnosed...[] Abstract Heterozygous GATA-2 germline mutations are associated with overlapping clinical manifestations termed GATA-2 deficiency, characterized by immunodeficiency and predisposition[] genes related to immature progenitor (IMP) cells.[] High-mobility group A proteins are nonhistone nuclear proteins that bind DNA and regulate the transcriptional activity of many genes.[] As chromosome 18 is the locus of the ferrochelatase gene, we postulate that this chromosomal deletion led to reduced synthesis of the enzyme in the bone marrow clone, so causing[] -HOXD13 protein, human Oncogene Proteins, Fusion PUMA protein, mouse Pmaip1 protein, mouse Proto-Oncogene Proteins c-bcl-2 Tumor Suppressor Protein p53 Tumor Suppressor Proteins[] Cytogenetic, molecular and microarray analysis of peripheral blood, skin fibroblasts and bone marrow revealed unusual results, suggestive of somatic chromosome instability[]

  • Nasal Polyp

    As such the sinus specialists at C/V ENT Surgical Group in Los Angeles have some of the lowest chances for revision sinus surgery in polyp patients.[] BACKGROUND: The actions of glucocorticoids in target tissues depend on the local metabolism of glucocorticoids catalyzed by 11β hydroxysteroid dehydrogenase (HSD) 1 and 2.[] Functional annotation results showed that several gene ontology (GO) terms were enriched in the list of genes with switched APA sites, including regulation of transcription[] We found numerical chromosome changes in one out of five cytogenetically investigated nasal polyps.[] The objective of this study is to determine whether 2 molecules associated with tissue damage (high mobility group box-1 [HMGB-1] and adenosine triphosphate [ATP]) elicit[] Mucosal Treg cells coexpressed both proteins.[] Expression of CD147 in groups 3 and 4 was significantly higher than in groups 1 and 2. CD98 expression was higher in groups 1, 2, and 3 than in group 4.[]

    Missing: (Nonhistone
  • Chronic Sinusitis

    A and group B, respectively.[] BACKGROUND: Sinonasal epithelial cells are recognized as drivers of inflammation in chronic sinusitis with nasal polyps (CRSwNP) through secretion of T helper 2 (Th2)-promoting[] Western blot analysis was performed to validate differential gene expression at the protein level.[] ) certain infectious and parasitic diseases ( A00-B99 ) complications of pregnancy, childbirth and the puerperium ( O00-O9A ) congenital malformations, deformations and chromosomal[] We conclude that PLUNC protein is an essential factor in the innate defense mechanism of the nasal mucosa.[] She had suffered weight loss and pain over a 2-month period.[] RESULTS: High-resolution, reproducible 2-DE patterns were obtained, and 30 differentially expressed protein spots were found.[]

    Missing: (Nonhistone
  • Retinoid

    F, Member 2/genetics Nuclear Receptor Subfamily 1, Group F, Member 2/metabolism Nuclear Receptor Subfamily 1, Group F, Member 2/physiology* Response Elements Transcription[] The Ordinary Granactive Retinoid 2% Emulsion was previously known as The Ordinary Advanced Retinoid 2%.[] In ultraviolet B (UVB) irradiated mouse skin, the expression of ATRA target genes is found to be reduced.[] BACKGROUND AND AIM: The HBV covalently closed circular DNA (cccDNA) is organized into a minichromosome in the nuclei of infected hepatocytes through interactions with histone and nonhistone[] The cytogenetic study did not show evidence of spontaneous or UV-induced chromosomal instability.[] […] retinol-binding proteins (CRBP) and cellular retinoic acid binding-proteins (CRABP). sRBP transports the highly lipophilic retinol through an aqueous medium.[] All results demonstrate that EGCG in combination with Am80 changes levels of acetylation in nonhistone proteins via down-regulation of HDAC4, -5 and -6 and stimulates apoptotic[]

    Missing: High Mobility
  • Placenta Previa

    The mRNA expression levels of HMGB1 and VEGF were significantly increased in the placenta previa group compared with in the normal group.[] Associated with 2-fold increase in congenital malformations Placenta accreta Vasa previa rupture of fetal vessels that cross the membranes covering the cervix treat with C-section[] She was heterozygous for the mutation G1691A for the gene of Leiden’s factor and homozygous for the mutation C677T of MTHFR’s gene.[] Cases of intrauterine growth restriction, pregnancy-induced hypertension, multiple pregnancies, fetal anomalies, chromosomal abnormalities, and maternal medical illnesses[] RESULTS: The following results were found: (1) 50 women were studied: 23 had morbidly adherent placenta, of which 12 (52.2%) were severe morbidly adherent placenta; (2) 2-[] The case group had higher nestin mRNA and protein levels throughout human fetal development.[] Fetal Diagn Ther. 2010;28(2):114-6. doi: 10.1159/000314038. Epub 2010 Jun 19.[]

    Missing: (Nonhistone
  • Skin Infection

    Background: Group A Streptococcus (GAS) skin infections are particularly prevalent in developing nations.[] RESULTS: Analysis of the primary end point showed noninferiority of dalbavancin in both DISCOVER 1 and DISCOVER 2.[] There was also increased expression of genes encoding virulence factors, namely secreted toxins and fibronectin and/or fibrinogen-binding proteins.[] […] oxacillin-susceptible-mecA-positive meticillin-resistant S. aureus (OS-MRSA) strains and MRSA isolates that harbour a divergent mecA homologue termed mecC within the novel staphylococcal cassette chromosome[] Child mobility (high) Reported by carer whether child sleeps at another dwelling at least one night in ten (or 10%). Child mobility high versus low mobility (reference).[] Antimicrobial proteins produced by snake venoms have recently attracted significant attention due to their relevance to bacterial infection and potential development into[] […] between 14 and 20 years (n 52), group 2, between 21 and 30 years (n 19) and group 3, aged ; 31 years (n 11).[]

    Missing: (Nonhistone
  • Eclampsia

    The mean serum concentration of TLR4 was 22.83 8.46 μg/L in the pre-eclampsia group versus 18.83 6.79 μg/L in the control group (P 0.057).[] Record 2, English Record 2, Subject field(s) Symptoms (Medicine) Pregnancy Record 2, Abbreviations, English Record 2, Synonyms, English Record 2, Textual support, English[] OBJECTIVES: To identify possible association between the selected HLA-G gene polymorphisms and risk of pre-eclampsia.[] The chromosome complement of the placenta and the neonate were 69,XXX and 46,XX, respectively.[] RESULTS: A total of 234 differential proteins were identified.[] The differentially expressed genes (DEG) were identified using the LIMMA package, and their potential functions were predicted by Gene Ontology (GO) enrichment analysis.[] […] as the control group.[]

    Missing: (Nonhistone
  • Herpes Simplex Virus 2

    BACKGROUND: HIV prevalence varies from 1.7% to 14.8% between ethnic groups in Uganda.[] Herpes Simplex Virus 2 (HSV-2) Infection An infection caused by herpes simplex virus 2 (HSV-2) and usually associated with lesions in the genital or anal area.[] Abstract The Us2 gene encodes a tegument protein that is conserved in most members of the Alphaherpesvirinae.[] Abstract We constructed a herpes simplex virus 2 (HSV-2) bacterial artificial chromosome (BAC) clone, bHSV2-BAC38, which contains full-length HSV-2 inserted into a BAC vector[] Gene variation and gene-environmental interactions involving the genes encoding the NMDA receptors are therefore likely to influence the risk of schizophrenia.[] The rates of spontaneous abortion and sexually transmitted disease were higher in the herpes virus 2 infection group than the healthy control group.[] Abstract Herpes simplex virus 2 (HSV-2) may cause frequent recurrences, highlighting its ability to evade host defense.[]

    Missing: (Nonhistone High Mobility
  • Congenital Dyserythropoietic Anemia

    Abstract Congenital dyserythropoietic anemias (CDAs) are a group of relatively rare inherited anemias.[] : 2/12/2014[] Future analysis of this locus may lead to the identification of a gene essential to normal erythropoiesis.[] Carrier Proteins Chromatin Chromosomal Proteins, Non-Histone Glycoproteins SEC23B protein, human Vesicular Transport Proteins codanin-1 protein, mouse heterochromatin-specific nonhistone[] A linkage analysis located a candidate region on chromosome 20, termed the CDAN2 locus, in the majority of CDAII patients but the aberrant gene has not so far been elucidated[] E2F proteins are the main regulator of G(1)/S transition.[] Abstract Congenital dyserythropoietic anemias (CDAs) are a group of hereditary disorders characterized by ineffective erythropoiesis and distinct morphological abnormalities[]

    Missing: High Mobility
  • Hypoxic-Ischemic Encephalopathy

    Group 2 (control group): Thirty full term healthy neonates.[] CrSO 2 increased more rapidly in infants with greater injury seen on MRI (0.20/h for MRI scores 0/1, by 0.48/h for MRI score 2, and by 0.68/h for MRI score 3, p 0.05).[] Thus, we aimed to explore the association between NOS3 gene polymorphisms and HIE susceptibility and symptoms in a Chinese Han population.[] BACKGROUND: We measured changes in the blood level of high-mobility group box-1 (HMGB-1) at 24 h intervals in neonates treated with brain/body hypothermia (body hypothermia[] BACKGROUND: Tau protein is s specific protein expressed by neurons in the central nervous system.[] We identified a novel frameshift mutation, p.Asp293GlyfsX10, in the SOX10 gene of this patient.[] […] with the control group (P 0.05).[]

    Missing: (Nonhistone Chromosomal)