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19 Possible Causes for Sema4c, mouse, protein

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  • Malignant Glioma

    Activation of Plexin-B2 by Sema4C ligand in glioblastoma cells induced actin-based cytoskeletal dynamics and invasive migration in vitro .[impactjournals.com] METHODS: The GL261-Luc2 intracranial mouse model of glioma was used to investigate the effects of the KD on the tumor-specific immune response.[ncbi.nlm.nih.gov] Citrullinated proteins were identified by mass spectrometry.[ncbi.nlm.nih.gov]

  • Cataract - Microcornea Syndrome

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] Categories Rare developmental defect during embryogenesis Rare eye disease Human Genes crystallin, alpha A crystallin, gamma D crystallin, beta B2 crystallin, gamma C Related Mouse[mousebook.org] These findings highlight the importance of protein-protein interactions among β-crystallins in maintaining lens transparency, and provide a novel insight into the molecular[ncbi.nlm.nih.gov]

  • Familial Benign Flecked Retina

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] Product Name Calcium-dependent phospholipase A2 (PLA2G5), Polyclonal Antibody Also Known As Rabbit anti-mouse Calcium-dependent phospholipase A2 polyclonal Antibody, HRP conjugated[mybiosource.com] […] with PLA2G5 recombinant protein[mybiosource.com]

  • Autosomal Dominant Optic Atrophy - Hearing Loss - Peripheral Neuropathy Syndrome

    (Sema Domain, Immunoglobulin Domain (Ig), Transmembrane Domain (TM) and Short Cytoplasmic Domain, (Semaphorin) 4C): SEMA4C antibodies SEMA4C ELISA Kits SEMA4C Proteins STK3[antibodies-online.com] Product name Description Mouse polyclonal to OPA3 Host species Mouse Tested applications Species reactivity Reacts with: Human Immunogen Full length human OPA3 protein (NP[abcam.com] This protein also sequesters cytochrome c.[genecards.org]

  • Knobloch Syndrome Type 1

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] Product name Mouse ES (Endostatin) ELISA Kit Catalogue No.[fn-test.com] BLASTX analysis revealed two exons with significant homology to a zebrafish protein (ES1) and an Escherichia coli protein (σ cross-reacting protein 27A), both of unknown function[link.springer.com]

  • Bothnia Retinal Dystrophy

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] Anti-RLBP1 monoclonal antibody (DCABH-7731) Rabbit anti-Human RLBP1 monoclonal antibody for WB, IP Datasheet Online Inquiry Add to basket Specifications Species Reactivity Mouse[creative-diagnostics.com] The protein folds into the prototypical SEC14-like domain structure and is most similar to α-tocopherol transfer protein (PDB code 1OIP ; overall sequence identity of 29%;[pnas.org]

  • Autosomal Recessive Isolated Optic Atrophy

    (Sema Domain, Immunoglobulin Domain (Ig), Transmembrane Domain (TM) and Short Cytoplasmic Domain, (Semaphorin) 4C): SEMA4C antibodies SEMA4C ELISA Kits SEMA4C Proteins STK3[antibodies-online.com] […] atrophy 3 protein; Optic atrophy 3 (Iraqi-Jewish 'optic atrophy plus') UniProt Protein Name Optic atrophy 3 protein UniProt Entry Name OPA3_HUMAN NCBI Summary for OPA3 The mouse[mybiosource.com] Symbol Name Synonyms Organism OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) FLJ22187, FLJ25932, MGA3, MGC75494, Optic atrophy 3 protein Homo[ihop-net.org]

  • Bradyopsia

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] View all 11 Nucleotide Accessions ExactAntigen RETINALDEHYDE Citation Map Electroretinography - Wikipedia, the free encyclopedia Save to citation manager [in a new window] MOUSE[drdiag.hu] proteins, offering the latest in research of RGS proteins.[books.google.com]

  • Jalili Syndrome

    […] dystrophy with inner retinal dysfunction and ganglion cell abnormalities Retinal nonattachment nonsyndromic congenital Retinitis pigmentosa juvenile Retinitis pigmentosa SEMA4C[qlinics.com] Human and mouse amelogenin gene loci are on the sex chromosomes. Genomics 1989;4:162-8. 24. Takagi Y, Fujita H, Katano H, Shimokawa H, Kuroda T.[jorthodsci.org] Once the genes and proteins are identified, expression patterns and function will be explored using immunohistochemistry and molecular and cellular biology techniques.[findaphd.com]

  • Anauxetic Dysplasia

    SCP2, SCRIB, SCT, SCUBE2, SDC3, SDCCAG8, SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD, SEC23A, SEC23B, SEC63, SECISBP2, SEL1L, SELE, SELL, SELP, SELPLG, SEMA3A, SEMA3E, SEMA4A, SEMA4C[inteligene.com.br] Models phenotype-based associations Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram.[mousephenotype.org] POP1 Human Genome Epidemiology (HuGE) Navigator POP1 Atlas of Genetics and Cytogenetics in Oncology and Haematology: POP1 No data available for Genatlas for POP1 Gene RNA-protein[genecards.org]