4.8 Article

Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Review Oncology

The tyrosine phosphatase Shp2 (PTPN11) in cancer

Gordon Chan et al.

CANCER AND METASTASIS REVIEWS (2008)

Article Multidisciplinary Sciences

Role of ERK1/2 signaling in congenital valve malformations in Noonan syndrome

Maike Krenz et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Medicine, Research & Experimental

Mediating ERK1/2 signaling rescues congenital heart defects in a mouse model of Noonan syndrome

Tomoki Nakamura et al.

JOURNAL OF CLINICAL INVESTIGATION (2007)

Article Cell Biology

The transcription factor MEF2C is required for craniofacial development

Michael P. Verzi et al.

DEVELOPMENTAL CELL (2007)

Article Endocrinology & Metabolism

Ras-MAPK signaling in osteogenic differentiation: Friend or foe?

Aaron Schindeler et al.

JOURNAL OF BONE AND MINERAL RESEARCH (2006)

Review Anatomy & Morphology

Recent advances in craniofacial morphogenesis

Yang Chai et al.

DEVELOPMENTAL DYNAMICS (2006)

Article Developmental Biology

Spatial and temporal patterns of ERK signaling during mouse embryogenesis

LB Corson et al.

DEVELOPMENT (2003)

Article Developmental Biology

Tissue origins and interactions in the mammalian skull vault

XB Jiang et al.

DEVELOPMENTAL BIOLOGY (2002)

Review Genetics & Heredity

Genetics of craniofacial development and malformation

AOM Wilkie et al.

NATURE REVIEWS GENETICS (2001)

Article Genetics & Heredity

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

LA Mavrogiannis et al.

NATURE GENETICS (2001)