Pages that link to "Q24336323"
Jump to navigation
Jump to search
The following pages link to PKD1 interacts with PKD2 through a probable coiled-coil domain (Q24336323):
Displaying 50 items.
- Polycystin 1, transient receptor potential channel interacting (Q2044253) (← links)
- Polycystin 2, transient receptor potential cation channel (Q21103321) (← links)
- A method for measuring electrical signals in a primary cilium (Q22001112) (← links)
- Identification of PKD2L, a human PKD2-related gene: tissue-specific expression and mapping to chromosome 10q25 (Q22008623) (← links)
- Specific association of the gene product of PKD2 with the TRPC1 channel (Q22009113) (← links)
- Polycystin-L is a calcium-regulated cation channel permeable to calcium ions (Q22010635) (← links)
- The polycystic kidney disease protein PKD2 interacts with Hax-1, a protein associated with the actin cytoskeleton (Q22253865) (← links)
- Interaction between LIS1 and doublecortin, two lissencephaly gene products (Q24290295) (← links)
- Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel (Q24290926) (← links)
- Polycystin-2 is an intracellular calcium release channel (Q24292332) (← links)
- The sequence, expression, and chromosomal localization of a novel polycystic kidney disease 1-like gene, PKD1L1, in human (Q24292360) (← links)
- Expression of PKD1 and PKD2 transcripts and proteins in human embryo and during normal kidney development (Q24292456) (← links)
- PIGEA-14, a novel coiled-coil protein affecting the intracellular distribution of polycystin-2 (Q24296682) (← links)
- Polycystin-1 and polycystin-2 regulate the cell cycle through the helix-loop-helix inhibitor Id2 (Q24297056) (← links)
- Polycystin-1 regulates the stability and ubiquitination of transcription factor Jade-1 (Q24299323) (← links)
- A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes (Q24300157) (← links)
- Nephrocystin-1 forms a complex with polycystin-1 via a polyproline motif/SH3 domain interaction and regulates the apoptotic response in mammals (Q24300420) (← links)
- Alpha-actinin associates with polycystin-2 and regulates its channel activity (Q24300429) (← links)
- PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells (Q24311878) (← links)
- Deficiency of polycystin-2 reduces Ca2+ channel activity and cell proliferation in ADPKD lymphoblastoid cells (Q24314239) (← links)
- Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects (Q24316109) (← links)
- Interaction between PKD1L3 and PKD2L1 through their transmembrane domains is required for localization of PKD2L1 at taste pores in taste cells of circumvallate and foliate papillae (Q24318877) (← links)
- NB4S, a member of the TBC1 domain family of genes, is truncated as a result of a constitutional t(1;10)(p22;q21) chromosome translocation in a patient with stage 4S neuroblastoma (Q24322761) (← links)
- Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations. (Q24336734) (← links)
- Polycystin 2 interacts with type I inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling (Q24338262) (← links)
- PKD2 interacts and co-localizes with mDia1 to mitotic spindles of dividing cells: role of mDia1 IN PKD2 localization to mitotic spindles (Q24338591) (← links)
- The structure of a PKD domain from polycystin-1: implications for polycystic kidney disease (Q24533517) (← links)
- Identification of the gene for oral-facial-digital type I syndrome (Q24536160) (← links)
- International Union of Basic and Clinical Pharmacology. LXXVI. Current progress in the mammalian TRP ion channel family (Q24623493) (← links)
- Mutations in a NIMA-related kinase gene, Nek1, cause pleiotropic effects including a progressive polycystic kidney disease in mice (Q24648390) (← links)
- Interaction between RGS7 and polycystin (Q24653605) (← links)
- A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2) (Q24678335) (← links)
- Role of calcium in polycystic kidney disease: From signaling to pathology (Q26770740) (← links)
- The functions of TRPP2 in the vascular system (Q26771361) (← links)
- The Role of G-Protein-Coupled Receptor Proteolysis Site Cleavage of Polycystin-1 in Renal Physiology and Polycystic Kidney Disease (Q26775090) (← links)
- A polycystin-centric view of cyst formation and disease: the polycystins revisited (Q26800974) (← links)
- Cilia functions in development (Q26829929) (← links)
- Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy (Q27000075) (← links)
- Novel role of ouabain as a cystogenic factor in autosomal dominant polycystic kidney disease (Q27011660) (← links)
- Polycystin-1 cleavage and the regulation of transcriptional pathways (Q27012570) (← links)
- Role of PKD2 in rheotaxis in Dictyostelium (Q27322406) (← links)
- Identification of MMP1 as a novel risk factor for intracranial aneurysms in ADPKD using iPSC models (Q27324613) (← links)
- Structural and molecular basis of the assembly of the TRPP2/PKD1 complex (Q27646334) (← links)
- X-ray Crystal Structure of a TRPM Assembly Domain Reveals an Antiparallel Four-stranded Coiled-coil (Q27652067) (← links)
- Crystal structure of a trimeric form of the KV7.1 (KCNQ1) A-domain tail coiled-coil reveals structural plasticity and context dependent changes in a putative coiled-coil trimerization motif (Q27657087) (← links)
- Structure of the EF-hand domain of polycystin-2 suggests a mechanism for Ca2+-dependent regulation of polycystin-2 channel activity (Q27661283) (← links)
- Molecular mechanism of the assembly of an acid-sensing receptor ion channel complex. (Q27675360) (← links)
- A high-resolution structure of the EF-hand domain of human polycystin-2 (Q27684526) (← links)
- A conserved signal and GTPase complex are required for the ciliary transport of polycystin-1. (Q28000060) (← links)
- Physiological mechanisms and therapeutic potential of bone mechanosensing. (Q28082204) (← links)