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70 Possible Causes for nek8, protein,, zebrafish

Did you mean: nek8, proteus, zebrafish

  • Nephronophthisis

    Nek8.[ncbi.nlm.nih.gov] protein complexes.[ncbi.nlm.nih.gov] This theory states that the products of all genes that are mutated in cystic kidney diseases in humans, mice, or zebrafish are expressed in primary cilia or centrosomes of[ncbi.nlm.nih.gov]

  • Nephronophthisis

    Here we identify ANKS6 as a new NPHP family member that connects NEK8 (NPHP9) to INVS (NPHP2) and NPHP3.[ncbi.nlm.nih.gov] Interstitial/genetics Nephritis, Interstitial/metabolism Substances Adaptor Proteins, Signal Transducing Membrane Proteins NPHP1 protein, human Grant support G0802359/Medical[ncbi.nlm.nih.gov] This theory states that the products of all genes that are mutated in cystic kidney diseases in humans, mice, or zebrafish are expressed in primary cilia or centrosomes of[ncbi.nlm.nih.gov]

  • Nephronophthisis

    Abstract Mutations in the never-in-mitosis A-related kinase, Nek8, are associated with cystic kidney disease in both humans and mice, with Nek8 being the NPHP9 gene in the[ncbi.nlm.nih.gov] Furthermore, sphere formation assays as well as the pronephros of elipsa zebrafish embryos showed defects in epithelialization.[ciliajournal.biomedcentral.com] The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development.[genecards.org]

  • Nephronophthisis

    In a subsequent study, it was found that NEK8 interacts with the ADPKD protein polycystin 2 and suggested that NEK8 may regulate both the expression and posttranslational[doi.org] The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development.[genecards.org] Furthermore, we produce a PKD-like renal cystic phenotype and randomization of heart looping by knockdown of invs expression in zebrafish.[ncbi.nlm.nih.gov]

  • Nephronophthisis

    Nek8.[ncbi.nlm.nih.gov] The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development.[genecards.org] Furthermore, sphere formation assays as well as the pronephros of elipsa zebrafish embryos showed defects in epithelialization.[ciliajournal.biomedcentral.com]

  • Nephronophthisis

    In a subsequent study, it was found that NEK8 interacts with the ADPKD protein polycystin 2 and suggested that NEK8 may regulate both the expression and posttranslational[doi.org] The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development.[genecards.org] Furthermore, sphere formation assays as well as the pronephros of elipsa zebrafish embryos showed defects in epithelialization.[ciliajournal.biomedcentral.com]

  • Nephronophthisis 4

    […] adolescent) NPHP3 CFAP31 FLI30691 FLI36696 KIAA2000 MKS7 NPH3 SLSN3 608002 7907 nephrocystin 4 nephronophthisis 4 NPHP4 KIAA0673 POC10 SLSN4 607215 19104 NIMA related kinase 8 NEK8[ukgtn.nhs.uk] 21555462 NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway Habbig, S , Bartram, MP , Müller, RU , Schwarz, R , Andriopoulos, N , Chen, S , Sägmüller[reactome.org] To study the role of nphp4 in establishing L-R asymmetry, we used antisense morpholinos to knockdown nphp4 expression in zebrafish.[lirias.kuleuven.be]

  • Nephronophthisis 16

    INVS, NPHP3, NPHP1, CEP290, NPHP4, IQCB1, AHI1, SDCCAG8, RPGRIP1L, NEK8, GLIS2, ANKS6 Specificity 9 % Genes 100 % KidneySeq - 264 Genes.[mendelian.co] JBTS4 Protein nephrocystin-1 Protein NPH1 Protein Nphp1 Protein SLSN1 Protein wu:fi59g07 Protein zgc:152930 Protein Bezeichner auf Proteinebene für NPHP1 juvenile nephronophthisis[antikoerper-online.de] Cilia 2012 1 (Suppl 1) :P103 Simms et al; licensee BioMed Central Ltd. 2012 Published: 16 November 2012 Keywords Zebrafish Embryo Morpholino Cystic Kidney Morpholino Oligonucleotide[ciliajournal.biomedcentral.com]

  • Hereditary Hypophosphatemic Rickets with Hypercalciuria

    JAK3, CD2AP, CFB, CFI, CFH, CFHR5, CD46, C3, THBD, GNAS, NR3C2, CFHR1, CFHR3, DGKE, ADAMTS13, APOL1, CDKN1B, KLHL3, B9D1, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, NEK8[mendelian.co] Pages: 1 NPT2C Polyclonal Antibody Gene Names: NPT2C ; SLC34A3; HHRH; NPTIIc Other Names: Sodium-dependent phosphate transport protein 2C; Sodium-phosphate transport protein[mybiosource.com] Instead, zebrafish, having the most complete fish genome sequence, has four NaP i cotransporter genes, two each belonging to the type IIa family and the more divergent type[ncbi.nlm.nih.gov]

  • Autosomal Recessive Primary Microcephaly

    , LMBRD1, LMX1B, LPIN1, LRP4, LYZ, MAFB, MAX, MBTPS2, MEFV, MET, MKKS, MKS1, MLH3, MLL2, MMAA, MMAB, MMACHC, MMADHC, MNX1, MTHFR, MTR, MTRR, MUT, MVK, MYH9, MYO1E, NEK1, NEK8[e-icm.net] Two previously reported (8508delGA, W1326X) and four novel sequence variants (Y1712X, I1717X, Y3353X, R3244X) were detected and all were predicted to be protein truncating[ncbi.nlm.nih.gov] Loss-of-function mutation in zebrafish sil has an embryonic lethal defect [ 98 ].[ncbi.nlm.nih.gov]