Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
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International Union of Basic and Clinical Pharmacology. LXXVI. Current progress in the mammalian TRP ion channel familyCongenital hydrocephalus in genetically engineered miceFunctional characterization of putative cilia genes by high-content analysisPkd1l1 establishes left-right asymmetry and physically interacts with Pkd2.Primary cilia are specialized calcium signalling organellesRegulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50.Carcinogens induce loss of the primary cilium in human renal proximal tubular epithelial cells independently of effects on the cell cycleNme gene family evolutionary history reveals pre-metazoan origins and high conservation between humans and the sea anemone, Nematostella vectensisNME7 is a functional component of the γ-tubulin ring complexStrain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2The gammaTuRC revisited: a comparative analysis of interphase and mitotic human gammaTuRC redefines the set of core components and identifies the novel subunit GCP8Cilia, calcium and the basis of left-right asymmetry.Transcriptional profiling of mouse uterus at pre-implantation stage under VEGF repression.Zygotic Porcn paternal allele deletion in mice to model human focal dermal hypoplasia.Acetylproteomic analysis reveals functional implications of lysine acetylation in human spermatozoa (sperm)Transposition of the great arteries and autosomal-dominant polycystic kidney disease.Exploring the elephant: histopathology in high-throughput phenotyping of mutant mice.Genetic Analysis Reveals a Hierarchy of Interactions between Polycystin-Encoding Genes and Genes Controlling Cilia Function during Left-Right Determination.Bi-allelic Mutations in PKD1L1 Are Associated with Laterality Defects in Humans.Polycystins and renovascular mechanosensory transduction.Calcium-mediated mechanisms of cystic expansion.Learning about the functions of NME/NM23: lessons from knockout mice to silencing strategies.Riding the wave of ependymal cilia: genetic susceptibility to hydrocephalus in primary ciliary dyskinesia.The primary cilium calcium channels and their role in flow sensing.Nucleoside diphosphate kinases (NDPKs) in animal development.A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.Evaluation of potential protein biomarkers in patients with high sperm DNA damage.Ciliary Mechanisms of Cyst Formation in Polycystic Kidney Disease.Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?Dentin Dysplasia in Notum Knockout Mice.The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development
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P2860
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
description
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
artikull shkencor
@sq
artículu científicu espublizáu en 2010
@ast
im Jahr 2010 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2010
@uk
مقالة علمية (نشرت عام 2010)
@ar
name
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@ast
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@en
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@nl
type
label
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@ast
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@en
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@nl
prefLabel
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@ast
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@en
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@nl
P2093
P2860
P921
P3181
P356
P1433
P1476
Situs inversus in Dpcd/Poll-/-, Nme7-/- , and Pkd1l1-/- mice
@en
P2093
P2860
P304
P3181
P356
10.1177/0300985809353553
P50
P577
2010-01-01T00:00:00Z