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19 Possible Causes for SEMA6A, human, protein

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  • Miglitol

    The assay exhibited a linear dynamic range of 100-6000 ng/mL for miglitol in human plasma.[ncbi.nlm.nih.gov] When signaling between Sema6A and PlexA2 was lost, not only highlight the need for a number buy miglitol without prescription of patients with diabetes are likely to have[iar.ch] (MCP)-1, plasminogen activator inhibitor-1, and fatty acid-binding protein 4, in type 2 diabetic patients for 3 months.[ncbi.nlm.nih.gov]

  • Chordoma

    A comparison of the gene expression profiles of the cell lines revealed significant differences in the expression of several genes like MAGEC2 and SEMA6A known to be associated[ncbi.nlm.nih.gov] Cell-cycle distribution and cell surface expression of proteins were analyzed by fluorescence-activated cell sorting (FACS) analysis.[ncbi.nlm.nih.gov] The immortalized human chordoma cells U-CH2 were used as in vitro model.[ncbi.nlm.nih.gov]

  • Kawasaki Disease

    Previous studies have suggested that human adenovirus (HAdV) is one of the triggering pathogens of KD.[ncbi.nlm.nih.gov] The male-specific association of FCGR2A, but not SEMA6A and IL17REL, was also replicated in a Japanese population (OR 1.74, P 1.04 10-4 in males vs.[ncbi.nlm.nih.gov] The identification of differentially expressed proteins and the underlying mechanisms may be the key to understanding differences between these KD complications.[ncbi.nlm.nih.gov]

  • Exfoliation Syndrome

    We identified association signals at 13q12 (POMP), 11q23.3 (TMEM136), 6p21 (AGPAT1), 3p24 (RBMS3) and 5q23 (near SEMA6A).[ncbi.nlm.nih.gov] This pathology is characterized by pathological accumulation of fibrillar protein in distinct ocular tissues, but protein deposits are mainly found in close proximity to the[symptoma.com] Human eyes with exfoliation syndrome (XFS) exhibit a distinctive pattern of iris transillumination defects that are recapitulated in Lyst mutant mice carrying the beige allele[ncbi.nlm.nih.gov]

  • Endometrial Stromal Sarcoma

    PDCD1LG2 TAL1 BCL2 CRLF2 FLT3 WT1 ABL2 BCL11B BCR CHD1 CSF1R EBF1 EPOR FGFR1 IKZF1 IKZF2 KLF2 KMT2A MLLT4 NF1 NTRK3 NUP214 NUP98 P2RY8 PAG1 PBX1 PDGFRB PICALM PTK2B RUNX1 SEMA6A[archerdx.com] , where the SS18-SSX fusion proteins disrupt the mSWI/SNF (BAF) chromatin remodeling complex.[ncbi.nlm.nih.gov] Eight primary LMS, 9 primary ESS and 8 metastatic LMS were analyzed for miRNA profiles using TaqMan Human miRNA Array Cards.[ncbi.nlm.nih.gov]

  • Usher Syndrome Type 1K

    Usher syndrome (USH) is an autosomal recessive disorder considered as the most common cause of hereditary deaf-blindness in human, accounting for over 50% of individuals who[mafiadoc.com] Semaphorin E, Sema E 85208 Q99985 10 9 Semaphorin 3F precursor Semaphorin IV, Sema IV, Sema III/F 88382 Q13275 8 9 Semaphorin 6A precursor Semaphorin VIA, Semaphorin 6A-1, SEMA6A[zonapse.net] […] network component harmonin 1 102,207,096 102,256,779 RGD:8547536 RGD:8554872 RGD:8695937 RGD:8695939 RGD:8694458 RGD:8694457 G Ush1g USH1 protein network component sans 10[rgd.mcw.edu]

  • Autosomal Recessive Spastic Paraplegia Type 72

    8q22 Select SARM1 sterile alpha and TIR motif containing 1 17q11 Select SCN7A sodium channel, voltage-gated, type VII, alpha 2q24.3 Select SELL selectin L 1q24.2 Select SEMA6A[alsod.iop.kcl.ac.uk] […] helix Phylogenomic databases Family and domain databases InterPro i View protein in InterPro IPR004345 TB2_DP1_HVA22 PANTHER i PTHR12300 PTHR12300, 1 hit Pfam i View protein[uniprot.org] Giovanni Stevanin , Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias , European Journal of Human[doi.org]

  • Autosomal Recessive Spastic Paraplegia Type 32

    human gene; 'D655N' corresponds to D555N in the human gene; 'E542A' corresponds to E442A in the human gene.][flybase.org] 8q22 Select SARM1 sterile alpha and TIR motif containing 1 17q11 Select SCN7A sodium channel, voltage-gated, type VII, alpha 2q24.3 Select SELL selectin L 1q24.2 Select SEMA6A[alsod.iop.kcl.ac.uk] To evaluate the effect of KLITL insertion on the protein conformation, we performed structural prediction of intradiol domain of wild-type and mutant Spatacsin protein by[omicsonline.org]

  • Nestor-Guillermo Progeria Syndrome

    Less than 1% of human primary somatic cells can usually turn into iPSCs.[aimspress.com] SEMA6A G:605885 . . SEMA6B G:608873 . . SEMA6C G:609294 . . SEMA6D G:609295 . . SEMA7A GP:607961 . [Blood group, John-Milton-Hagen] (3) SEMG1 G:182140 . .[usegalaxy.org] Cell signaling mechanisms often transmit information via posttranslational protein modifications, most importantly reversible protein phosphorylation.[scienceopen.com]

  • Carcinomatous Polyarthritis

    We identified association signals at 13q12 (POMP), 11q23.3 (TMEM136), 6p21 (AGPAT1), 3p24 (RBMS3) and 5q23 (near SEMA6A).[science.gov] Cell nologies of DNA transfection and somatic cell fusion in the surface carbohydrates, cytoskeletal proteins, glycoproteins, exploration of molecular aspects of metastatic[books.google.de] Inflammation is one of the human body's reactions to disease or injury, and includes swelling, pain, and quite often, stiffness.[disabled-world.com]