Pages that link to "Q24324759"
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The following pages link to Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene (Q24324759):
Displaying 50 items.
- T-box transcription factor 1 (Q21175001) (← links)
- T-box 1 (Q21980210) (← links)
- Identification, mapping, and phylogenomic analysis of four new human members of the T-box gene family: EOMES, TBX6, TBX18, and TBX19 (Q22008666) (← links)
- Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome (Q22010499) (← links)
- Differential DNA binding and transcription modulation by three T-box proteins, T, TBX1 and TBX2 (Q24290598) (← links)
- Identification of a novel nuclear localization signal in Tbx1 that is deleted in DiGeorge syndrome patients harboring the 1223delC mutation (Q24294577) (← links)
- Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions (Q24295078) (← links)
- TBX10, a member of the Tbx1-subfamily of conserved developmental genes, is located at human chromosome 11q13 and proximal mouse chromosome 19 (Q24328944) (← links)
- Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios (Q24538580) (← links)
- Genomic disorders on 22q11 (Q24563977) (← links)
- Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice (Q28204189) (← links)
- DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1 (Q28204282) (← links)
- DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion (Q28205158) (← links)
- Chromosomal microdeletions: dissecting del22q11 syndrome (Q28206335) (← links)
- DiGeorge's syndrome: a gene at last (Q28213375) (← links)
- RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction (Q28216207) (← links)
- 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome (Q28217633) (← links)
- The T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegans (Q28345297) (← links)
- TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome (Q28512803) (← links)
- A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2 (Q28587320) (← links)
- Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos (Q28589938) (← links)
- Enamel-free teeth: Tbx1 deletion affects amelogenesis in rodent incisors (Q28593230) (← links)
- Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data (Q30849515) (← links)
- The embryonic genes Dkk3, Hoxd8, Hoxd9 and Tbx1 identify muscle types in a diet-independent and fiber-type unrelated way. (Q33540865) (← links)
- Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities (Q33708603) (← links)
- A comprehensive analysis of 22q11 gene expression in the developing and adult brain (Q33717638) (← links)
- Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies (Q34009396) (← links)
- An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome (Q34148921) (← links)
- Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease (Q34214613) (← links)
- T-box genes in development: from hydra to humans. (Q34250613) (← links)
- Transcription factors in cardiogenesis: the combinations that unlock the mysteries of the heart (Q34562988) (← links)
- Strong evidence that GNB1L is associated with schizophrenia (Q34713665) (← links)
- Zebrafish cardiac development requires a conserved secondary heart field (Q34966448) (← links)
- TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome (Q35234113) (← links)
- Syndromic immunodeficiencies: genetic syndromes associated with immune abnormalities (Q35621987) (← links)
- Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome. (Q35950127) (← links)
- How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease. (Q36131140) (← links)
- Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation (Q36359225) (← links)
- Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population. (Q36891185) (← links)
- Early de novo DNA methylation and prolonged demethylation in the muscle lineage. (Q36891931) (← links)
- When half is not enough: gene expression and dosage in the 22q11 deletion syndrome (Q36914294) (← links)
- Identification of microdeletions in candidate genes for cleft lip and/or palate (Q36929652) (← links)
- 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development (Q37669766) (← links)
- Regulation of organogenesis and stem cell properties by T-box transcription factors. (Q38088192) (← links)
- Gene expression profile of amyloid beta protein-injected mouse model for Alzheimer disease (Q38325876) (← links)
- Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis (Q39096808) (← links)
- Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia. (Q39159190) (← links)
- Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity. (Q40186459) (← links)
- A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease (Q41345961) (← links)
- Genetics and management of the patient with orofacial cleft (Q41659078) (← links)