Pages that link to "Q24533160"
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The following pages link to Identification and functional analysis of ZIC3 mutations in heterotaxy and related congenital heart defects (Q24533160):
Displaying 50 items.
- Identification and functional analysis of CITED2 mutations in patients with congenital heart defects (Q24294854) (← links)
- Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination (Q24306605) (← links)
- Characterization of TBX20 in human hearts and its regulation by TFAP2 (Q24313555) (← links)
- Functional and structural basis of the nuclear localization signal in the ZIC3 zinc finger domain (Q24324680) (← links)
- Characterization of the interactions of human ZIC3 mutants with GLI3 (Q24338829) (← links)
- VACTERL/VATER Association (Q24600367) (← links)
- SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing (Q24614096) (← links)
- A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation (Q24631597) (← links)
- The genetic landscape and clinical implications of vertebral anomalies in VACTERL association (Q26753049) (← links)
- Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key Player (Q26775087) (← links)
- Genetics of congenital heart disease: the glass half empty (Q26862793) (← links)
- Of mice and men: molecular genetics of congenital heart disease (Q26995476) (← links)
- Spectrum of clinical diseases caused by disorders of primary cilia (Q27024881) (← links)
- DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia (Q27309156) (← links)
- Mouse model of heterotaxy with single ventricle spectrum of cardiac anomalies (Q28509213) (← links)
- Heart defects in X-linked heterotaxy: evidence for a genetic interaction of Zic3 with the nodal signaling pathway (Q28594057) (← links)
- Expression of the zic1, zic2, zic3, and zic4 genes in early chick embryos (Q33606243) (← links)
- BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects (Q33677028) (← links)
- The determination factors of left-right asymmetry disorders- a short review (Q33693300) (← links)
- Identification of a Novel ZIC3 Isoform and Mutation Screening in Patients with Heterotaxy and Congenital Heart Disease (Q34000038) (← links)
- Review of genetic factors in intestinal malrotation (Q34013406) (← links)
- Birth of a healthy boy after PGD for X-linked heterotaxy syndrome (Q34037136) (← links)
- Genetic basis of congenital cardiovascular malformations (Q34125381) (← links)
- A mouse model of conduction system patterning abnormalities in heterotaxy syndrome (Q34134301) (← links)
- Heterotaxy-spectrum heart defects in Zic3 hypomorphic mice (Q34252634) (← links)
- Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy. (Q34448317) (← links)
- Duplication and deletion of CFC1 associated with heterotaxy syndrome (Q34449443) (← links)
- Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy (Q34495112) (← links)
- Disorders caused by chromosome abnormalities (Q34775497) (← links)
- Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations (Q34898379) (← links)
- Xenopus: An emerging model for studying congenital heart disease (Q35075360) (← links)
- The prevalence of clinical features associated with primary ciliary dyskinesia in a heterotaxy population: results of a web-based survey (Q35206397) (← links)
- Zic3 is required for maintenance of pluripotency in embryonic stem cells. (Q35723737) (← links)
- Changing Faces of Transcriptional Regulation Reflected by Zic3 (Q35742138) (← links)
- Heterozygous deletion of FOXA2 segregates with disease in a family with heterotaxy, panhypopituitarism, and biliary atresia. (Q35770210) (← links)
- An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis. (Q35803129) (← links)
- Preaxial polydactyly caused by Gli3 haploinsufficiency is rescued by Zic3 loss of function in mice (Q35856281) (← links)
- A human laterality disorder associated with a homozygous WDR16 deletion (Q35959700) (← links)
- The zinc finger gene ZIC2 has features of an oncogene and its overexpression correlates strongly with the clinical course of epithelial ovarian cancer (Q36091016) (← links)
- Unraveling the pathogenesis and etiology of biliary atresia (Q36092178) (← links)
- New Genetic Insights into Congenital Heart Disease (Q36106143) (← links)
- Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature (Q36230701) (← links)
- The Role of the Geneticist and Genetic Counselor in an ACHD Clinic (Q36292010) (← links)
- Genetics of human heterotaxias (Q36298333) (← links)
- Hearts with isomerism of the right atrial appendages - one of the worst forms of disease in 2005. (Q36317160) (← links)
- Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry (Q36412975) (← links)
- Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left-right patterning and heart development (Q36709672) (← links)
- Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly (Q36744686) (← links)
- Emerging roles for zic genes in early development (Q36748446) (← links)
- Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterning (Q36787200) (← links)