Keywords: سیلیوپاتی; PKHD1; renal replacement therapy; oligohydramnios; ciliopathy; AIC; Akaike information criterion; ARPKD; Autosomal recessive polycystic kidney disease; AUC; Area under the curve; CVVH; Continuous venovenous hemofiltration; PD; Peritoneal dialysis;
مقالات ISI سیلیوپاتی (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سیلیوپاتی; PC1/2; Pkd1/2, polycystin 1/2; TRPV4; transient receptor potential vanilloid 4; AC6; adenylyl cyclase 6; cAMP; cyclic adenosine monophosphate; IFT88; intraflagellar transport 88; Kif3a; kinesin family member 3A; HDAC6; histone deacetylase 6; BBS; Bardet-B
Keywords: سیلیوپاتی; Renal cysts; Ciliopathy; Nephronophthisis; NGS;
Keywords: سیلیوپاتی; Cilia; Ciliopathy; Fuz; Fgf8; Neural crest; Craniofacial; Skull; Calvaria; Coronal suture; Greig cephalopolysyndactyly; Morphogenesis; Craniosynostosis; Wnt1; Mesp1; Mouse;
Alström syndrome: Renal findings in correlation with obesity, insulin resistance, dyslipidemia and cardiomyopathy in 38 patients prospectively evaluated at the NIH clinical center
Keywords: سیلیوپاتی; Alström syndrome; ALMS1; Ciliopathy; Insulin resistance; Metabolic syndrome; Chronic kidney disease;
Advances in the Genetics of Primary Ciliary Dyskinesia
Keywords: سیلیوپاتی; axoneme; bronchiectasis; cilia; ciliopathy; mucociliary clearance; PCD; primary ciliary dyskinesia;
Cilia - The sensory antennae in the eye
Keywords: سیلیوپاتی; Cilia; Ciliopathy; Eye; Retina; Degeneration; Therapy;
Ciliopathies: Does HDAC6 Represent a New Therapeutic Target?
Keywords: سیلیوپاتی; cilium; ciliopathy; ciliary disassembly; HDAC6; HDAC6 inhibitor
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum
Keywords: سیلیوپاتی; Joubert syndrome; Meckel-Gruber syndrome; Multiple sequence alignment; Evolutionary conservation; MKS1; Corpus-Callosum agenesis; Genotype-phenotype correlation; Ciliopathy; Dysmorphology; Syndromology; Bioinformatics; Missense-mutation; Founder mutation
Quoi de neuf en dermatologie pédiatrique ?
Keywords: سیلیوپاتی; Anomalies vasculaires; Bêtabloquants; Sirolimus; Atopie; Psoriasis; Scabiose; STAT; Ciliopathie; Vascular anomalies; PHACE; Betablockers; Sirolimus; Atopy; Psoriasis; Scabies; STAT; Ciliopathy;
c21orf59/kurly Controls Both Cilia Motility and Polarization
Keywords: سیلیوپاتی; Kurly (Kur); c21orf59; cilia; planar cell polarity; disheveled; ciliopathy; primary ciliary dyskinesia; multiciliated cell
Zebrafish as a Model for Human Ciliopathies
Keywords: سیلیوپاتی; Cilia; Zebrafish; Ciliopathy; Disease model
An age of enlightenment for cilia: The FASEB summer research conference on the “Biology of Cilia and Flagella”
Keywords: سیلیوپاتی; Arl3; Arl13b; Axoneme; Bardet-Biedl syndrome (BBS); Calcium; Ciliopathy; Ciliary membrane; Craniofacial defects; Diabetes; Dynein; GPCR; Hedgehog signaling; Intraflagellar transport (IFT); Motility; NPHP; Obesity; Phosphoinositide; Polycystin; Transitio
Bardet-Biedl syndrome: A model for translational research in rare diseases
Keywords: سیلیوپاتی; AAV; adeno-associated vector; ADPKD; autosomal dominant polycystic kidney disease; BBS; Bardet-Biedl Syndrome; CDE; common data element; CRIBBS; Clinical Registry Investigating Bardet-Biedl Syndrome; DDAVP; desmopressin acetate; GRDR®; Global Rare Di
IFT46 plays an essential role in cilia development
Keywords: سیلیوپاتی; Cilia; Ciliopathy; IFT; Intraflagellar transport; IFT46; KO mouse; L/R defect; Zebrafish;
RPGR: Its role in photoreceptor physiology, human disease, and future therapies
Keywords: سیلیوپاتی; Ciliopathy; Retinitis pigmentosa; RPGR; Human disease; Animal model; Stem cell; Gene therapy;
Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish
Keywords: سیلیوپاتی; poc1b; Photoreceptor sensory cilia (PSC); Basal body; Ciliopathy; Zebrafish; Inherited retinal degenerations (IRDs);
Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing
Keywords: سیلیوپاتی; Ciliopathy; Joubert syndrome and related disorders; Bardet-Biedl syndrome; Meckel syndrome; Homozygosity mapping; Mutation frequencies;
Dynein and intraflagellar transport
Keywords: سیلیوپاتی; Cytoplasmic dynein 2; Intraflagellar transport; Ciliopathy;
A case of Bardet-Biedl syndrome complicated with intracranial hypertension in a Japanese child
Keywords: سیلیوپاتی; Bardet-Biedl syndrome (BBS); Cilia; Ciliopathy; Intracranial hypertension
Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings
Keywords: سیلیوپاتی; Cardiomyopathy; Alström syndrome; ALMS1; Exome sequencing; Ciliopathy
Senior-Loken syndrome: A novel NPHP5 gene mutation in a family from Kuwait
Keywords: سیلیوپاتی; ESRF, end stage renal failure; S-L, Senior-Loken; NPHP, nephronophthisis; BUN, blood urea nitrogenArab; Ciliopathy; Consanguinity; Nephronophthisis; Senior-Loken syndrome; Premarital counselling
12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4
Keywords: سیلیوپاتی; Ciliopathy; Gene deletion; CEP290; Meckel syndrome
Acrocallosal syndrome: Identification of a novel KIF7 mutation and evidence for oligogenic inheritance
Keywords: سیلیوپاتی; Acrocallosal syndrome; KIF7 mutation; Ciliopathy; Primary cilia
Molecular views of Arf-like small GTPases in cilia and ciliopathies
Keywords: سیلیوپاتی; Arl; Small GTPase; Ciliopathy; Cilia
Late survival in Ellis-van Creveld syndrome - A case report
Keywords: سیلیوپاتی; Ellis-van Creveld syndrome; Ciliopathy; Short rib narrow thorax syndromes;
From quantitative protein complex analysis to disease mechanism
Keywords: سیلیوپاتی; Cilium; Intraflagellar transport; Ciliopathy; Affinity purification; Protein complex analysis; SF-TAP; SILAC; Mass spectrometry; Disease mechanism; Leber’s congenital amaurosis
Severe aortic stenosis, bicuspid aortic valve and atrial septal defect in a child with Joubert Syndrome and Related Disorders (JSRD) - A case report and review of congenital heart defects reported in the human ciliopathies
Keywords: سیلیوپاتی; Ciliopathy; Joubert Syndrome and Related Disorders; Aortic stenosis; Bicuspid aortic valve; Atrial septal defect; Congenital heart disease;
The ciliary transitional zone and nephrocystins
Keywords: سیلیوپاتی; Primary cilia; Renal epithelia; Ciliopathy
Senior–Løken syndrome: A syndromic form of retinal dystrophy associated with nephronophthisis
Keywords: سیلیوپاتی; NPHP, nephronophthisis; NPHP5, nephrocystin-5; SLS, Senior–Løken syndrome; RP, retinitis pigmentosaSenior–Løken syndrome; Nephronophthisis; Nephrocystins; Retinal degeneration; Ciliopathy; Primary cilium
Current mutation discovery approaches in Retinitis Pigmentosa
Keywords: سیلیوپاتی; Ciliopathy; Next Generation Sequencing; Photoreceptor; Rod; Cone
Putative roles of cilia in polycystic kidney disease
Keywords: سیلیوپاتی; Cilia; Development; Wnt; Hedgehog; mTOR; Ciliopathy
Retinal dystrophy in Bardet–Biedl syndrome and related syndromic ciliopathies
Keywords: سیلیوپاتی; Bardet–Biedl syndrome; Ciliopathy; Connecting cilium/Primary cilium; Retinitis pigmentosa
The role of primary cilia in neuronal function
Keywords: سیلیوپاتی; Ciliopathy; Joubert syndrome; Neuronal function; Primary cilia
Primary ciliary dyskinesia: when to suspect the diagnosis and how to confirm it
Keywords: سیلیوپاتی; primary ciliary dyskinesia; bronchiectasis; ciliopathy; rhinitis; situs inversus; light microscopy; electron microscopy; nasal nitric oxide
Le syndrome de Bardet-Biedl
Keywords: سیلیوپاتی; Bardet-Biedl syndrome; BBS gene; Multicystic kidneys; Rod-cone dystrophy; Pigmentary retinopathy; Ciliopathy; Primary cilia; Obesity; Oligogenism; Triallelic inheritance; Mental disabilitySyndrome de Bardet-Biedl; Gène BBS; Reins multikystiques; Rétinopat