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11 Possible Causes for HIF 1beta, human, protein

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  • Hypoxia

    -1alpha and IL-1beta Expression in Insulin Resistance Elizabeth J.[keystonesymposia.org] BLAST Align Show all Add to basket E9PJ21 E9PJ21_HUMAN Hypoxia up-regulated protein 1 HYOU1 656 Annotation score: J3QL06 J3QL06_HUMAN Hypoxia up-regulated protein 1 HYOU1[uniprot.org] Human chondrocytes isolated from articular cartilage obtained post‑mortally and human mesenchymal stem cells derived from bone marrow (BM‑MSCs) were seeded onto a collagen‑based[ncbi.nlm.nih.gov]

  • Anemia of Chronic Disease

    Abstract Anemia is the most frequently encountered hematologic complication in human immunodeficiency virus (HIV) infection and acquired immunodeficiency syndrome.[ncbi.nlm.nih.gov] In the present study, we examined the ability of both K-11706, which inhibits GATA and enhances HIF-1 binding activity, and K-13144, which has no effect on GATA or HIF-1 binding[ncbi.nlm.nih.gov] Acute-phase proteins, such as hepcidin, as well as pro- and anti-inflammatory cytokines affect iron acquisition and release pathways of monocytes and macrophages thereby leading[ncbi.nlm.nih.gov]

  • Neonatal Hypoxic and Ischemic Brain Injury

    During hypoxia, HIF-1alpha protein is stabilized and heterodimerizes with HIF-1beta to form HIF-1, subsequently regulating the expression of target genes.[ncbi.nlm.nih.gov] In the present study, we sought to investigate the efficacy of human neural stem cells derived from human embryonic stem cells in a rat model of neonatal HI and the mechanisms[ncbi.nlm.nih.gov] Bcl-2 and bax protein expression were also analyzed with immunohistochemistry.[ncbi.nlm.nih.gov]

  • Weaver Syndrome

    Abstract The biological processes controlling human growth are diverse, complex and poorly understood.[ncbi.nlm.nih.gov] PMID 22622284 MicroRNA-101 negatively regulates Ezh2 and its expression is modulated by androgen receptor and HIF-1alpha/HIF-1beta.[atlasgeneticsoncology.org] Synonym(s): EZH2 Protein Complex, EZH2 , PRC2, Enhancer Of Zeste Homolog 2; RBAP48, Retinoblastoma Binding Protein 4 (RBBP4), NURF55, Chromatin Assembly Factor 1 Subunit C[bpsbioscience.com]

  • BCG Vaccine

    Sialylated and non-sialylated forms of the recombinant human lactoferrin (rhLF), glycoengineered in yeast (Pichia pastoris) and expressing humanized N-glycosylation patterns[ncbi.nlm.nih.gov] Succinate is an inflammatory signal that induces IL-1beta through HIF-1alpha. Nature 496 , 238–242 (2013). 42. Krawczyk, C. M. et al.[doi.org] Western-blot showed that the secretive recombinant proteins could specifically combine with antibody against M. tuberculosis HSP65, indicating that the recombinant proteins[ncbi.nlm.nih.gov]

  • Dilated Cardiomyopathy Type 2B

    Global variation in copy number in the human genome. Nature 2006; 444:444-454. 9. Lock DP, Sharp AJ, McCarroll SA et al.[books.google.com] -1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 T47D MCF7 K562 ARNTL Basic helix-loop-helix factors (bHLH)PublicBMAL1, BMAL1c, JAP3, MOP3, PASD3, TIC, bHLHe5 U2OS ARRB1[tagc.univ-mrs.fr] The remaining proteins play various roles within cardiomyocytes to ensure their proper functioning.[ghr.nlm.nih.gov]

  • Homozygous 11p15-p14 Deletion Syndrome

    Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. ‏[books.google.com] -1beta, HIF1-beta, HIF-1-beta - ARNT and Prostate Cancer 6 CXCL5 4q13.3 SCYB5, ENA-78 - CXCL5 and Prostate Cancer 6 CXCR2 2q35 CD182, IL8R2, IL8RA, IL8RB, CMKAR2, CDw128b[cancer-genetics.org] In addition to epigenetic inactivation, the viral Tax protein has been shown to inhibit p73 functions [ 46 , 47 ].[hindawi.com]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    -1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00000100[genome.jp] Hall Oxford University Press , 27 oct. 2005 - 1520 páginas This widely acclaimed reference work gives a comprehensive survey of all significant human malformations and related[books.google.es] OMIM ID Human Disease OMIM:211390 Sabinas Brittle Hair Syndrome OMIM:268700 Saccharopinuria OMIM:615709 Sacral Agenesis with Vertebral Anomalies; SAVA OMIM:600145 Sacral Defect[informatics.jax.org]

  • 1p32-p31 Deletion Syndrome

    DEL1P32P31 Summary Gene Symbol DEL1P32P31 Entrez Gene ID 100532738 Full Name Chromosome 1p32-p31 deletion syndrome Synonyms C1DELp32p31 Gene Type unknown Organism Homo sapiens(human[genscript.com] -1beta, HIF1-beta, HIF-1-beta Somatic- Breast Cancer - Lung Cancer - Prostate Cancer S100A10 1q21 42C, P11, p10, GP11, ANX2L, CAL1L, CLP11, Ca[1], ANX2LG - Esophageal Cancer[cancerindex.org] […] receptor Background Formyl peptide receptor 1 (FPR1) is a G protein-coupled receptor mainly expressed from the cells of myeloid source, where it mediates the innate immune[bios-mep.info]

  • Atrial Standstill

    -1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA, TANGO, bHLHe2 aryl hydrocarbon receptor nuclear translocator C00001510 411 ARSB, ASB, G4S, MPS6 arylsulfatase B (EC:3.1.6.12[genome.jp] The encoded protein is an integral membrane protein with sequence motifs characteristic of the presenilin-type aspartic proteases.[genecards.org] In recent decades, cases of partial atrial standstill have been recognized in humans.[pubag.nal.usda.gov]