Pages that link to "Q28591574"
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The following pages link to Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention (Q28591574):
Displaying 50 items.
- A conditional knockout resource for the genome-wide study of mouse gene function (Q21735918) (← links)
- WNK lysine deficient protein kinase 1 (Q21992578) (← links)
- The knockout mouse project (Q22122054) (← links)
- The thiazide-sensitive Na-Cl cotransporter is regulated by a WNK kinase signaling complex (Q24299205) (← links)
- WNK1 phosphorylates synaptotagmin 2 and modulates its membrane binding (Q24302525) (← links)
- The double-histone-acetyltransferase complex ATAC is essential for mammalian development (Q24310357) (← links)
- Antagonistic regulation of ROMK by long and kidney-specific WNK1 isoforms (Q24537454) (← links)
- Functional interactions of the SPAK/OSR1 kinases with their upstream activator WNK1 and downstream substrate NKCC1 (Q24548301) (← links)
- Molecular physiology of the thiazide-sensitive sodium-chloride cotransporter (Q24598213) (← links)
- Serum and glucocorticoid-induced kinase (SGK) 1 and the epithelial sodium channel are regulated by multiple with no lysine (WNK) family members (Q24633684) (← links)
- Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II (Q24648539) (← links)
- WNK kinases, renal ion transport and hypertension (Q24649138) (← links)
- WNK1 and OSR1 regulate the Na+, K+, 2Cl- cotransporter in HeLa cells (Q24676697) (← links)
- Tagging genes with cassette-exchange sites (Q24799039) (← links)
- Suppression of nonsense-mediated mRNA decay permits unbiased gene trapping in mouse embryonic stem cells (Q24802839) (← links)
- High-throughput trapping of secretory pathway genes in mouse embryonic stem cells. (Q25255826) (← links)
- Conditional gene expression in the mouse inner ear using Cre-loxP. (Q26991845) (← links)
- A molecular update on pseudohypoaldosteronism type II (Q27000474) (← links)
- Mouse RC/BTB2, a member of the RCC1 superfamily, localizes to spermatid acrosomal vesicles (Q27300124) (← links)
- Neuroinflammation, mitochondrial defects and neurodegeneration in mucopolysaccharidosis III type C mouse model. (Q27303930) (← links)
- Disruption of the Golgi protein Otg1 gene causes defective hormone secretion and aberrant glucose homeostasis in mice. (Q27320877) (← links)
- Loss of the putative catalytic domain of HDAC4 leads to reduced thermal nociception and seizures while allowing normal bone development (Q27345064) (← links)
- RhoE deficiency produces postnatal lethality, profound motor deficits and neurodevelopmental delay in mice (Q27345530) (← links)
- Small-molecule WNK inhibition regulates cardiovascular and renal function (Q27644248) (← links)
- WNK1 activates ERK5 by an MEKK2/3-dependent mechanism (Q28234991) (← links)
- Lipid-lowering effects of anti-angiopoietin-like 4 antibody recapitulate the lipid phenotype found in angiopoietin-like 4 knockout mice (Q28235182) (← links)
- Insertional mutagenesis in mice: new perspectives and tools (Q28259871) (← links)
- WNK1: analysis of protein kinase structure, downstream targets, and potential roles in hypertension (Q28305389) (← links)
- Characterization of PTPRG in knockdown and phosphatase-inactive mutant mice and substrate trapping analysis of PTPRG in mammalian cells (Q28483906) (← links)
- Keratinocyte migration in the developing eyelid requires LIMK2 (Q28484233) (← links)
- Targeted disruption of leucine-rich repeat kinase 1 but not leucine-rich repeat kinase 2 in mice causes severe osteopetrosis (Q28505157) (← links)
- Regulators of the proteasome pathway, Uch37 and Rpn13, play distinct roles in mouse development (Q28505259) (← links)
- Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice (Q28505979) (← links)
- Murine UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase lacking the gamma-subunit retains substantial activity toward acid hydrolases (Q28506485) (← links)
- Congenital hydrocephalus in genetically engineered mice (Q28506486) (← links)
- Tubulin tyrosine ligase-like 1 deficiency results in chronic rhinosinusitis and abnormal development of spermatid flagella in mice (Q28512199) (← links)
- ADP-ribosylation factor-like 3 is involved in kidney and photoreceptor development (Q28512728) (← links)
- Dominant-negative regulation of WNK1 by its kidney-specific kinase-defective isoform (Q28567514) (← links)
- Identification of the WNK-SPAK/OSR1 signaling pathway in rodent and human lenses (Q28581906) (← links)
- The WNK1 and WNK4 protein kinases that are mutated in Gordon's hypertension syndrome phosphorylate and activate SPAK and OSR1 protein kinases (Q28583124) (← links)
- Mice lacking mannose 6-phosphate uncovering enzyme activity have a milder phenotype than mice deficient for N-acetylglucosamine-1-phosphotransferase activity (Q28584902) (← links)
- Hypomorphic mutation of the TALE gene Prep1 (pKnox1) causes a major reduction of Pbx and Meis proteins and a pleiotropic embryonic phenotype (Q28586917) (← links)
- A novel protein, CHRONO, functions as a core component of the mammalian circadian clock (Q28588364) (← links)
- Cardiomyopathy in α-kinase 3 (ALPK3)-deficient mice (Q28589708) (← links)
- Af17 deficiency increases sodium excretion and decreases blood pressure (Q28590130) (← links)
- PTH stimulates bone formation in mice deficient in Lrp5 (Q28592421) (← links)
- Hepatocyte growth factor activator inhibitor-1 (HAI-1) is essential for the integrity of basement membranes in the developing placental labyrinth (Q28593159) (← links)
- Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null mice (Q28593754) (← links)
- Abnormal cardiac development in the absence of heart glycogen (Q28594636) (← links)
- Conditional and inducible gene recombineering in the mouse inner ear (Q30444031) (← links)