Inversin (INVS) ELISA Kits

Xenopus laevis Inversin (INVS) Interaktionspartner

1. Inversin relays Frizzled-8 (zeige FZD8 ELISA Kits) signals to promote proximal pronephros development.

2. The present study indicates that calmodulin binding sites (IQ motifs) are crucial in controlling the biological activity of both mouse and Xenopus inv proteins

Human Inversin (INVS) Interaktionspartner

1. Collectively, these results indicated that inversin might promote the tumorigenicity of lung cancer cells and serve as a novel therapeutic target of non-small cell lung cancer.

2. Akt (zeige AKT1 ELISA Kits) phosphorylates inversin at amino acids 864-866 that are required not only for Akt (zeige AKT1 ELISA Kits) interaction, but also for inversin dimerization.

3. Truncating mutations in NPHP2 gene is associated with nephronophthisis-related ciliopathy.

4. ANKS6 as a new NPHP family member that assembles a distinct module of nephronophthisis-associated proteins, encompassing NEK8, INVS and NPHP3.

5. INVS mutation can cause juvenile nephronophthisis with abnormal reactivity of the Wnt (zeige WNT2 ELISA Kits)/beta-catenin (zeige CTNNB1 ELISA Kits) pathway.

6. has conserved ankyrin repeat and IQ domains and interacts with calmodulin

7. analysis of a homozygous mutation in exon 13 of inversin (INVS) (C2719T, R907X) in a patient with retinitis pigmentosa and renal failure [case report]

8. Thus, although considered a common variant, inv(10)(p11.2q21.2) has a single ancestral founder among northern Europeans.

9. Cystic kidney disease has been linked to mutations in the Invs gene in mice with an inversion of embryonic turning (inv/inv) and the INVS (NPHP2) gene in human infantile nephronophthisis (NPH).

10. screened 43 families with infantile nephronophthisis (ESRD less than 5 years of age) for NPHP2 and NPHP3 mutations and determined genotype-phenotype correlations

Mouse (Murine) Inversin (INVS) Interaktionspartner

1. We constructed sub-congenic lines to more specifically localize the modifier and have determined it resides in a 3.2 Mb interval containing 28 genes. These include Invs and Anks6, which are both excellent candidates for the modifier as mutations in these genes result in PKD (zeige PRKD1 ELISA Kits) and both genes are known to genetically and physically interact with Nek8.

2. Ciliary abnormalities are associated with nphp2 mutant mice.

3. Loss of NPHP2 causes ciliogenesis defects.

4. the significance of Inversin in controlling cell migration processes

5. Nek8 acts downstream of Inv function

6. Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia.

7. the inv gene product functions in several cellular compartments, including the nucleus and cell-cell adhesion sites

8. Molecular cloning of a gene for inversion of embryo turning (inv) with cystic kidney. Deduced amino acid sequence shows 15 successive repeats of Ank/Swi6 motif in its N-terminal domain. Mutation causes situs inversus and cysts in kidney in inv mutant.

9. inv has a role in kidney disease: inv mutant mouse has renal cysts resembling infantile NPHP2

10. The localization of inversin in distal tubules in the kidney and in extrarenal tissues suggests that the expression of this protein has an important function in a variety of organs.

Zebrafish Inversin (INVS) Interaktionspartner

1. Nek8 acts downstream of Inv function