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Keywords: 22q11.2 deletion syndrome
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Journal Articles
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx
Free
Journal:
Development
Development (2020) 147 (3): dev185256.
Published: 3 February 2020
..., in a distribution established in the early embryo. We further show that biallelic expression of the CPM regulatory gene Tbx1 , haploinsufficient in 22q11.2 deletion syndrome patients, is required for the correct patterning of muscles with CPM-derived connective tissue. Our results suggest that CPM plays...
Includes: Supplementary data
Journal Articles
Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors
Available to Purchase
Journal:
Development
Development (2004) 131 (21): 5491–5502.
Published: 1 November 2004
... into two distinct vessels(Yutzey and Kirby, 2002). Human chromosomal deletion syndromes are common causes of birth defects,but the complex and rare nature of such deletions have made a mechanistic analysis of the developmental anomalies elusive. 22q11.2 deletion syndrome(22q11DS), the most common...