Results 101 to 110 of about 5,757 (204)

Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21 [PDF]

open access: yes, 2010
Tbx1(-/-) mice present with phenotypic effects observed in DiGeorge syndrome patients however, the molecular mechanisms of Tbx1 regulating craniofacial and tooth development are unclear.
S. Florez   +19 more
core   +1 more source

Mesodermal Tbx1 is required for patterning the proximal mandible in mice

open access: yesDevelopmental Biology, 2010
Defects in the lower jaw, or mandible, occur commonly either as isolated malformations or in association with genetic syndromes. Understanding its formation and genetic pathways required for shaping its structure in mammalian model organisms will shed light into the pathogenesis of malformations in humans.
Aggarwal, Vimla S.   +5 more
openaire   +2 more sources

The 22q11.2 Deletion Syndrome: A Gene Dosage Perspective

open access: yesThe Scientific World Journal, 2006
The 22q11.2 deletion/DiGeorge syndrome is a relatively common “genomic” disorder that results from heterozygous deletion of a 3-Mbp segment of chromosome 22.
Antonio Baldini
doaj   +1 more source

Tbx2a and Tbx1 do not regulate expression of each other.

open access: yes, 2013
Fold-change of the expression level of Tbx2a and Tbx1 relative to the control (1x change) at 30 hpf. (A) tbx2a MO2 and MO3 had no significant effect on the expression of tbx1. (B) tbx1 MO had no significant effect on the expression of tbx2a.
Vladimir Korzh (53927)   +4 more
core   +1 more source

A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome

open access: yesDisease Models & Mechanisms, 2022
Gabriella Lania   +9 more
doaj   +1 more source

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

open access: yesBMC Medical Genetics, 2011
Background Conotruncal heart defects (CTDs) are present in 75-85% of patients suffering from the 22q11.2 deletion syndrome. To date, no consistent phenotype has been consistently correlated with the 22q11.2 deletions. Genetic studies have implicated TBX1
Xu Yue-Juan   +10 more
doaj   +1 more source

Tbx1 interacts with Baf60a in mouse embryo tissues.

open access: yes, 2012
(A) Co-IP experiment showing interaction of the Tbx1 and Baf60a endogenous proteins in embryo tissues. The first lane on the left contains nuclear extracts from E9.5 WT embryos.
Li Chen (5749)   +5 more
core   +1 more source

Analysis of TBX1 Variation in Patients with Psychotic and Affective Disorders

open access: yesMolecular Medicine, 2007
A significant portion of patients with 22q11 deletion syndrome (22q11DS) develop psychiatric disorders, including schizophrenia and other psychotic and affective symptoms, and the responsible gene/s are assumed to also play a significant role in the etiology of nonsyndromic psychiatric disease.
Birgit H, Funke   +9 more
openaire   +2 more sources

Regulatory effect of transcription factor TBX1 on osteogenic differentiation of human dental pulp stem cells [PDF]

open access: yesKouqiang yixue
Objective To investigate the regulatory effect of T-box transcription factor 1 (TBX1) on the osteogenic differentiation capacity of human dental pulp stem cells (hDPSCs) and its underlying mechanism.
WANG Mingxi, GAO Shan, LI Guoqing, TANG Chunbo
doaj  

Regulation of Sema3c and the Interaction between Cardiac Neural Crest and Second Heart Field during Outflow Tract Development

open access: yesScientific Reports, 2017
The cardiac neural crest cells (cNCCs) and the second heart field (SHF) play key roles in development of the cardiac outflow tract (OFT) for establishment of completely separated pulmonary and systemic circulations in vertebrates. A neurovascular guiding
Kazuki Kodo   +8 more
doaj   +1 more source

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