scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0165-6147(00)01832-0 |
P698 | PubMed publication ID | 11698076 |
P2093 | author name string | Zhou J | |
Stayner C | |||
P2860 | cites work | Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein | Q22001473 |
Identification of PKD2L, a human PKD2-related gene: tissue-specific expression and mapping to chromosome 10q25 | Q22008623 | ||
Polycystin-L is a calcium-regulated cation channel permeable to calcium ions | Q22010635 | ||
Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2) | Q22010947 | ||
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defects | Q24316109 | ||
Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation | Q24317412 | ||
The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains | Q24336814 | ||
Interaction between RGS7 and polycystin | Q24653605 | ||
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease | Q28345772 | ||
Polycystin 1 is required for the structural integrity of blood vessels | Q28512594 | ||
Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents | Q29615755 | ||
The cytoplasmic C-terminal fragment of polycystin-1 regulates a Ca2+-permeable cation channel | Q31484726 | ||
Identification and characterization of a novel polycystin family member, polycystin-L2, in mouse and human: sequence, expression, alternative splicing, and chromosomal localization | Q33897416 | ||
The genetics and physiology of polycystic kidney disease | Q34179146 | ||
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue. | Q35787062 | ||
Identification and characterization of polycystin-2, the PKD2 gene product | Q38320261 | ||
The pathology of human renal cystic disease. | Q40447184 | ||
The polycystic kidney disease 1 gene product modulates Wnt signaling | Q40973635 | ||
The endoplasmic reticulum Ca2+ store: a view from the lumen | Q41710104 | ||
Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease | Q42645641 | ||
Multilocus polycystic disease | Q44412153 | ||
The polycystic kidney disease-1 protein, polycystin-1, binds and activates heterotrimeric G-proteins in vitro | Q48364885 | ||
Transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X. | Q50716491 | ||
Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease. | Q52171297 | ||
Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations. | Q53879309 | ||
Polycystic kidney disease: The complete structure of the PKD1 gene and its protein | Q56535688 | ||
The polycystic kidney disease 1 gene product mediates protein kinase C alpha-dependent and c-Jun N-terminal kinase-dependent activation of the transcription factor AP-1 | Q74299216 | ||
Somatic inactivation of Pkd2 results in polycystic kidney disease | Q74502174 | ||
Identification of phosphorylation sites in the PKD1-encoded protein C-terminal domain | Q77854949 | ||
Identification of the major site of in vitro PKA phosphorylation in the polycystin-1 C-terminal cytosolic domain | Q77865503 | ||
P433 | issue | 11 | |
P304 | page(s) | 543-546 | |
P577 | publication date | 2001-11-01 | |
P1433 | published in | Trends in Pharmacological Sciences | Q2451474 |
P1476 | title | Polycystin channels and kidney disease. | |
P478 | volume | 22 |
Q42621739 | A third sea urchin sperm receptor for egg jelly module protein, suREJ2, concentrates in the plasma membrane over the sperm mitochondrion |
Q35822230 | Calcium at fertilization and in early development |
Q24314239 | Deficiency of polycystin-2 reduces Ca2+ channel activity and cell proliferation in ADPKD lymphoblastoid cells |
Q53551189 | Differences in renal tubule primary cilia length in a mouse model of Bardet-Biedl syndrome. |
Q40673214 | Expression of polycystin-1 C-terminal fragment enhances the ATP-induced Ca2+ release in human kidney cells |
Q35094105 | From genes to integrative physiology: ion channel and transporter biology in Caenorhabditis elegans |
Q34582336 | Intracellular calcium release modulates polycystin-2 trafficking |
Q35916409 | Invertebrate TRP proteins as functional models for mammalian channels |
Q24297056 | Polycystin-1 and polycystin-2 regulate the cell cycle through the helix-loop-helix inhibitor Id2 |
Q28505110 | Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells |
Q28260546 | Regulation of calcium signaling by polycystin-2 |
Q40450435 | The cytoplasmic C-terminus of polycystin-1 increases cell proliferation in kidney epithelial cells through serum-activated and Ca(2+)-dependent pathway(s). |
Q24292360 | The sequence, expression, and chromosomal localization of a novel polycystic kidney disease 1-like gene, PKD1L1, in human |
Q30834303 | Virtual-tissue computer simulations define the roles of cell adhesion and proliferation in the onset of kidney cystic disease |
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