4.5 Article

Neurofibromin (Nf1) is required for skeletal muscle development

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

KEGG for representation and analysis of molecular networks involving diseases and drugs

Minoru Kanehisa et al.

NUCLEIC ACIDS RESEARCH (2010)

Review Genetics & Heredity

Skeletal Abnormalities in Neurofibromatosis Type 1: Approaches to Therapeutic Options

Florent Elefteriou et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)

Article Cell Biology

MEK1 plays contrary stage-specific roles in skeletal myogenic differentiation

Chulman Jo et al.

CELLULAR SIGNALLING (2009)

Article Cardiac & Cardiovascular Systems

Cardiomyocyte-Specific Loss of Neurofibromin Promotes Cardiac Hypertrophy and Dysfunction

Junwang Xu et al.

CIRCULATION RESEARCH (2009)

Article Cell Biology

Muscle Contraction Is Necessary to Maintain Joint Progenitor Cell Fate

Joy Kahn et al.

DEVELOPMENTAL CELL (2009)

Article Medicine, General & Internal

Modelling neurofibromatosis type 1 tibial dysplasia and its treatment with lovastatin

Mateusz Kolanczyk et al.

BMC MEDICINE (2008)

Article Biochemistry & Molecular Biology

Multiple roles for neurofibromin in skeletal development and growth

Mateusz Kolanczyk et al.

HUMAN MOLECULAR GENETICS (2007)

Article Biochemistry & Molecular Biology

Neurofibromin plays a critical role in modulating osteoblast differentiation of mesenchymal stem/progenitor cells

Xiaohua Wu et al.

HUMAN MOLECULAR GENETICS (2006)

Article Genetics & Heredity

Double inactivation of NF1 in tibial pseudarthrosis

DA Stevenson et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2006)

Article Biochemistry & Molecular Biology

MEKK1 signaling through p38 leads to transcriptional inactivation of E47 and repression of skeletal Myogenesis

JL Page et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2004)

Article Physiology

Progression of kyphosis in mdx mice

N Laws et al.

JOURNAL OF APPLIED PHYSIOLOGY (2004)

Article Medicine, Research & Experimental

Disruption of either the Nfkb1 or the Bcl3 gene inhibits skeletal muscle atrophy

RB Hunter et al.

JOURNAL OF CLINICAL INVESTIGATION (2004)

Article Biochemistry & Molecular Biology

Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

SH Lecker et al.

FASEB JOURNAL (2004)

Review Anatomy & Morphology

Regulation of myogenic differentiation in the developing limb bud

PH Francis-West et al.

JOURNAL OF ANATOMY (2003)

Article Developmental Biology

Role of Runx genes in chondrocyte differentiation

S Stricker et al.

DEVELOPMENTAL BIOLOGY (2002)

Article Biochemistry & Molecular Biology

Activated MEK1 binds the nuclear MyoD transcriptional complex to repress transactivation

RLS Perry et al.

MOLECULAR CELL (2001)

Article Endocrinology & Metabolism

UCP2 muscle gene transfer modifies mitochondrial membrane potential

A Marti et al.

INTERNATIONAL JOURNAL OF OBESITY (2001)

Article Cell Biology

Genes that control the development of migrating muscle precursor cells

C Birchmeier et al.

CURRENT OPINION IN CELL BIOLOGY (2000)