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12 Possible Causes for PEBP1, human, protein

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  • Low-Grade Astrocytoma

    By 12 h of IL-4 treatment, both cdk4 and cdk2 kinase activities against the retinoblastoma protein (pRb) were reduced and nuclear entry of pRb was prohibited.[ncbi.nlm.nih.gov] […] nucleophosmin (NPM1), glucose regulated protein 78 kDa (GRP78), nucleolin (NCL) and heat shock protein 90 kDa (HSP90B1) were increased, Raf kinase inhibitor protein (RKIP/PEBP1[ncbi.nlm.nih.gov] We produced a single-chain human recombinant antibody (scFv), L19, which reacts specifically with B-FN and selectively targets tumor vasculature in vivo.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Hypocalcemia Type 1

    12q24.23 PBP, HCNP, PEBP, RKIP, HCNPpp, PEBP-1, HEL-210, HEL-S-34 - PEBP1 and Colorectal Cancer 7 NR4A2 2q22-q23 NOT, RNR1, HZF-3, NURR1, TINUR - NR4A2 and Colorectal Cancer[cancer-genetics.org] CaSR Polyclonal Antibody for Human CaSR Polyclonal Antibody for Human CaSR Polyclonal Antibody for Human CaSR Polyclonal Antibody for Human CaSR Monoclonal Antibody for Human[eiaab.com] G-protein activation.[uir.ulster.ac.uk]

  • Homozygous 11p15-p14 Deletion Syndrome

    12q24.23 PBP, HCNP, PEBP, RKIP, HCNPpp, PEBP-1, HEL-210, HEL-S-34 - PEBP1 and Prostate Cancer 5 HRK 12q24.22 DP5, HARAKIRI - HRK and Prostate Cancer 5 FLNC 7q32-q35 ABPA,[cancer-genetics.org] Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. ‏[books.google.com] Severe mutations lead to absent protein, mild-mod mutations to abnormal protein.[quizlet.com]

  • Nestor-Guillermo Progeria Syndrome

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] Less than 1% of human primary somatic cells can usually turn into iPSCs.[aimspress.com] Cell signaling mechanisms often transmit information via posttranslational protein modifications, most importantly reversible protein phosphorylation.[scienceopen.com]

  • Susceptibility to Malignant Cutaneous Melanoma 9

    […] corresponding Spanish minor allele frequency (MAF) differed from that published in HapMap (p- value CDK4 , rs3731239 in CDKN1A , rs2303942 in FASTK , rs2497 in GDI2 , rs2088702 in PEBP1[journals.plos.org] References: ICD10CM:C43 ICD10CM:C43.9 ICD9CM:172 ICD9CM:172.9 MESH:C562393 NCI:C3510 OMIM:608035 OMIM:612263 SNOMEDCT_US_2018_03_01:93655004 UMLS_CUI:C0151779 Ontology: Human[zfin.org] Proteinprotein BLAST ( ) against the Swiss-Prot database reveals homology between RASEF and a melanoma transforming oncogene, c-MEL (also known as RAB8A, a member of the[academic.oup.com]

  • AICA-Ribosiduria

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] […] line (HepG2), sarcoma osteogenic cells (Saos-2), human embryonic kidney cells (HEK293), human skin fibroblasts (SF) and primary human keratinocytes (KC) cultured in purine-depleted[ncbi.nlm.nih.gov] AICAR induction of TXNIP depended on MondoA, but was independent of AMPK (AMP-activated protein kinase) activation and calcium.[biochemj.org]

  • Combined Oxidative Phosphorylation Deficiency Type 24

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] […] the biology of human nutrition at the molecular, cellular, tissue, and whole-body levels.[books.google.de] View all proteins of this organism that are known to be involved in the pathway polypeptide chain elongation and in Protein biosynthesis .[uniprot.org]

  • Combined Oxidative Phosphorylation Deficiency Type 3

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] Western blot - AIF Human Profiling ELISA Kit (ab126583) Anti-AIF antibody [7F7AB10] ( ab110327 ) at 5 µg/ml Human heart tissue lysate - mitochondrial extract ( ab110337 )[abcam.com] ; decreases the levels of mitochondrial protein synthesis.[uniprot.org]

  • Premature Chromatid Separation Trait

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] The sequence of events was haploid groupings of the chromosomes in normal, human metaphase cells, followed by genomic doubling to homozygousdiploidy.[file.scirp.org] Contains 1 protein kinase domain.[abcam.com]

  • Microcephalic Primordial Dwarfism due to ZNF335 Deficiency

    PEBP1 G:604591 . . PEBP4 G:612473 . . PECAM1 G:173445 . . PECR G:605843 . . PEE1 P:189800 . . PEF1 G:610033 . . PEG10 G:609810 . . PEG3 G:601483 . . PELI3 G:609827 . .[usegalaxy.org] Human genomes (the complete set of genes or genetic material present in a cell or organism) consist of 3 million DNA base pairs.[dna.universeofatoms.com] […] in InterPro IPR036236 Znf_C2H2_sf IPR013087 Znf_C2H2_type SMART i View protein in SMART SM00355 ZnF_C2H2, 13 hits SUPFAM i SSF57667 SSF57667, 7 hits PROSITE i View protein[uniprot.org]