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Purpose:Noonan syndrome (NS) is an autosomal-dominant disorder characterized by craniofacial dysmorphism, growth retardation… Expand To the Editor: We read with great interest the article by Kouz et al.1 reporting on genotype–phenotype correlations of patients… Expand Mutations in RIT1, involved in the RAS‐MAPK pathway, have recently been identified as a cause for Noonan syndrome. We present two… Expand RIT1, (Ras-like without CAAX1), the founding member of a novel branch of the Ras subfamily, mediates a wide variety of cellular… Expand Noonan syndrome (NS) is an autosomal dominant disorder consisting of short stature, short and/or webbed neck, distinctive facial… Expand CTIP2 is a key transcriptional regulator involved in numerous physiological functions. Initial works have shown the importance of… Expand Background We have demonstrated earlier that CTIP2 is highly expressed in mouse skin during embryogenesis and in adulthood. CTIP2… Expand Abstract: Chicken ovalbumin upstream promoter‐transcription factor‐interacting protein 2 (CTIP2) is a transcriptional regulator… Expand Chicken ovalbumin upstream promoter transcription factor-interacting proteins 1 and 2 (CTIP1 and CTIP2) are related… Expand Allelic loss (LOH) mapping and sequence analysis were conducted for gamma-ray induced mouse thymic lymphomas and a novel tumor… Expand