Keywords: سندرم باردت-بیدل; 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
مقالات ISI سندرم باردت-بیدل (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: سندرم باردت-بیدل; AD; autosomal dominant; ADNIV; autosomal dominant neovascular inflammatory vitreoretinopathy; AR; autosomal recessive; AR-1; autosomal recessive-1 allele identified; ARMS; amplification refractory mutation system; AZOOR; acute zonal occult outer retinopat
Keywords: سندرم باردت-بیدل; extraaxial CSF; olfactory; choroid plexus; hippocampus; motile cilia; BBS; Bardet-Biedl syndrome; CHD; Congenital heart disease; CM; Ciliary motion; CP; Choroid plexus; CSF; Cerebrospinal fluid; CUS; Cranial ultrasound; MRI; Magnetic resonance imaging; RA
Keywords: سندرم باردت-بیدل; Rhodopsin; Trafficking; Cilium; Arfs; Rabs; ADRP; Autosomal Dominant Retinitis Pigmentosa; BBS; Bardet-Biedl Syndrome; BBSome; a conserved complex of BBS proteins; CTS; Ciliary Targeting Signal; DHA; Docosahexaenoic Acid; GAP; GTPase Activating Protein; G
Keywords: سندرم باردت-بیدل; Obstructive sleep apnea; Sleep disordered breathing; Bardet-Biedl Syndrome; Obesity; Polysomnography; Apnea-hypopnea index;
The ciliary protein Rpgrip1l in development and disease
Keywords: سندرم باردت-بیدل; BB; Basal body; Bbs; Bardet-Biedl syndrome; C. elegans; Caenorhabditis elegans; CC; Coiled-Coil; Cep290; Centrosomal Protein 290; COACH; Cerebellar Vermis Aplasia Oligophrenia Congenital Ataxia Coloboma Hepatic Fibrosis; CRD; Cone Rod Dystrophy; Cux1; Cut
Non-syndromic retinitis pigmentosa
Keywords: سندرم باردت-بیدل; Retinitis pigmentosa; Rod-cone dystrophy; Inherited retinal dystrophy; Phenotype; Genotype-phenotype correlation; RP subtype; BBS; Bardet-Biedl syndrome; cGMP; cyclic guanosine monophosphate; CSNB; congenital stationary night blindness; ESCs; embryotic st
Full Length ArticleBardet-Biedl syndrome 3 regulates the development of cranial base midline structures
Keywords: سندرم باردت-بیدل; Primary cilia; Craniofacial development; Sonic Hedgehog (SHH); Cell migration; Bardet-Biedl Syndrome;
Structural and molecular bases of rod photoreceptor morphogenesis and disease
Keywords: سندرم باردت-بیدل; Photoreceptor; Cryo-electron tomography; Retinal imaging; Retinal degeneration; Disease mechanisms; Ciliopathies; ADRP; autosomal dominant retinitis pigmentosa; BBS; Bardet-Biedl syndrome; BBSome; membrane coat complex formed by BBS gene products; Cryo-ET
Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes
Keywords: سندرم باردت-بیدل; Bardet-Biedl syndrome; Next-generation sequencing; Mutation; Phenotype–genotype correlation
Algoritmo para el estudio molecular del síndrome de Bardet-Biedl en España
Keywords: سندرم باردت-بیدل; Ciliopatías; Prevalencia; Síndrome de Bardet-Biedl; Algoritmo diagnósticoCiliopathies; Prevalence; Bardet-Biedl syndrome; Diagnosis algorithm
TRIM-NHL proteins in development and disease
Keywords: سندرم باردت-بیدل; TRIM; NHL; Brat; Mei-P26; TRIM32; LIN-41; TRIM71; Bardet-Biedl syndrome; Limb girdle muscular dystrophy 2H; Sarcotubular myopathy;
Syndromic ciliopathies: From single gene to multi gene analysis by SNP arrays and next generation sequencing
Keywords: سندرم باردت-بیدل; Ciliopathy; Joubert syndrome and related disorders; Bardet-Biedl syndrome; Meckel syndrome; Homozygosity mapping; Mutation frequencies;
Ciliopathies: The Central Role of Cilia in a Spectrum of Pediatric Disorders
Keywords: سندرم باردت-بیدل; ARPKD; Autosomal recessive polycystic kidney disease; BBS; Bardet-Biedl syndrome; CHD; Congenital heart disease; CHF; Congenital hepatic fibrosis; CNS; Central nervous system; PCD; Primary ciliary dyskinesia; RP; Retinitis pigmentosa; SI; Situs inversus t
What’s new in… Ciliopathies
Keywords: سندرم باردت-بیدل; ADPKD; ARPKD; Bardet-Biedl syndrome; centrosomes; cilia; ciliopathies; cysts; Meckel-Gruber syndrome; nephronopthisis; polycystic kidney disease
Diagnostic anténatal des reins hyperéchogènes : à propos de 17 cas
Keywords: سندرم باردت-بیدل; Diagnostic anténatal; Reins hyperéchogènes; Ãchographie prénatale; Polykystose rénale récessive; Polykystose rénale dominante; Syndrome de Bardet-Biedl; Prenatal diagnosis; Hyperechogenic kidneys; Prenatal ultrasonography; Recessive polycystic kid
From retinal circuitry to eye diseases—In memory of Henk Spekreijse
Keywords: سندرم باردت-بیدل; Retinal synaptic circuitry; Bipolar cells; Amacrine cells; Ganglion cells; Connexins; Guanylate cyclase activating proteins; Basic helix loop helix transcription factors; Spinocerebellar Ataxia; Bardet-Biedl Syndrome
Zmiany okulistyczne w zespole Bardeta i Biedla - opis przypadku
Keywords: سندرم باردت-بیدل; zespóÅ Bardeta-Biedla; retinopatia barwnikowa; otyÅoÅÄ; Bardet-Biedl syndrome; retinal dystrophy; obesity;
Hirschsprung's disease in Arab siblings with Bardet-Biedl syndrome
Keywords: سندرم باردت-بیدل; Hirschsprung's disease; Bardet-Biedl syndrome; Aganglionosis; Autosomal recessive
Retinal degeneration in children: Dark adapted visual threshold and arteriolar diameter
Keywords: سندرم باردت-بیدل; Bardet-Biedl syndrome; Leber congenital amaurosis; Usher syndrome; Dark adapted threshold; Retinal vasculature; Retinal degeneration; Rod mediated visual sensitivity
Le syndrome de Bardet-Biedl
Keywords: سندرم باردت-بیدل; 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
Temporal expression pattern of Bardet-Biedl syndrome genes in adipogenesis
Keywords: سندرم باردت-بیدل; Bardet-Biedl syndrome; Adipogenesis; 3T3-F442A; Obesity; Adipose tissue
Le point sur le syndrome de Bardet-Biedl
Keywords: سندرم باردت-بیدل; Syndrome de Bardet-Biedl; rétinite pigmentaire; tri allélisme; cil connecteur; Bardet-Biedl syndrome; retinitis pigmentosa; ciliogenesis; triallelism;
Mouse mutants as models for congenital retinal disorders
Keywords: سندرم باردت-بیدل; animal model; retina; mouse; gene mutation; retinal degeneration; BBS; Bardet-Biedl syndrome; ENU; N-ethyl-N-nitrosourea; ERG; electroretinogram; LCA; Leber's congenital amaurosis; RP; retinitis pigmentosa; RPE; retinal pigment epithelium; STGD; Stargardt