Related references
Note: Only part of the references are listed.The CMT4B disease-causing proteins MTMR2 and MTMR13/SBF2 regulate AKT signalling
Philipp Berger et al.
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2011)
Phosphoinositide Regulation of Integrin Trafficking Required for Muscle Attachment and Maintenance
Ines Ribeiro et al.
PLOS GENETICS (2011)
Autophagy inhibition induces atrophy and myopathy in adult skeletal muscles
Eva Masiero et al.
AUTOPHAGY (2010)
Drosophila Mtm and class II PI3K coregulate a PI(3)P pool with cortical and endolysosomal functions
Michaella Velichkova et al.
JOURNAL OF CELL BIOLOGY (2010)
Cytosolic FoxO1 is essential for the induction of autophagy and tumour suppressor activity
Ying Zhao et al.
NATURE CELL BIOLOGY (2010)
Valproic Acid Activates the PI3K/Akt/mTOR Pathway in Muscle and Ameliorates Pathology in a Mouse Model of Duchenne Muscular Dystrophy
Praveen B. Gurpur et al.
AMERICAN JOURNAL OF PATHOLOGY (2009)
FoxO1 induces apoptosis in skeletal myotubes in a DNA-binding-dependent manner
Thomas J. McLoughlin et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2009)
Changing phosphoinositides on the fly: how trafficking vesicles avoid an identity crisis
Roberto J. Botelho
BIOESSAYS (2009)
A Phosphoinositide Switch Controls the Maturation and Signaling Properties of APPL Endosomes
Roberto Zoncu et al.
CELL (2009)
Control of autophagy initiation by phosphoinositide 3-phosphatase jumpy
Isabelle Vergne et al.
EMBO JOURNAL (2009)
MTMR9 Increases MTMR6 Enzyme Activity, Stability, and Role in Apoptosis
Jun Zou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Dlg1, Sec8, and Mtmr2 Regulate Membrane Homeostasis in Schwann Cell Myelination
Annalisa Bolis et al.
JOURNAL OF NEUROSCIENCE (2009)
T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase
Lama Al-Qusairi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Loss of Myotubularin Function Results in T-Tubule Disorganization in Zebrafish and Human Myotubular Myopathy
James J. Dowling et al.
PLOS GENETICS (2009)
β2-Integrins contribute to skeletal muscle hypertrophy in mice
Joseph S. Marino et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2008)
The glucocorticoid receptor and FOXO1 synergistically activate the skeletal muscle atrophy-associated MuRF1 gene
David S. Waddell et al.
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM (2008)
The endosomal protein Appl1 mediates akt substrate specificity and cell survival in vertebrate development
Annette Schenck et al.
CELL (2008)
PIKfyve: Partners, significance, debates and paradoxes
Assia Shisheva
CELL BIOLOGY INTERNATIONAL (2008)
Skeletal Muscle-Specific Ablation of raptor, but Not of rictor, Causes Metabolic Changes and Results in Muscle Dystrophy
C. Florian Bentzinger et al.
CELL METABOLISM (2008)
Essential function of TORC2 in PKC and Akt turn motif phosphorylation, maturation and signalling
Tsuneo Ikenoue et al.
EMBO JOURNAL (2008)
The mammalian target of rapamycin complex 2 controls folding and stability of Akt and protein kinase C
Valeria Facchinetti et al.
EMBO JOURNAL (2008)
Sequential actions of myotubularin lipid phosphatases regulate endosomal PI(3)P and growth factor receptor trafficking
Canhong Cao et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Endosomal phosphoinositides and human diseases
Anne-Sophie Nicot et al.
TRAFFIC (2008)
Phosphoinositides and Charcot-Marie-Tooth disease: New keys to old questions
U. Suter
CELLULAR AND MOLECULAR LIFE SCIENCES (2007)
FoxO3 controls autophagy in skeletal muscle in vivo
Cristina Mammucari et al.
CELL METABOLISM (2007)
FoxO3 coordinately activates protein degradation by the Autophagic/Lysosomal and proteasomal pathways in atrophying muscle cells
Jinghui Zhao et al.
CELL METABOLISM (2007)
被撤回的出版物: FOXO1 regulates the expression of 4E-BP1 and inhibits mTOR signaling in mammalian skeletal muscle (Retracted Article. See vol 284, pg 20440, 2009)
Robert J. Southgate et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
AKT/PKB signaling: Navigating downstream
Brendan D. Manning et al.
CELL (2007)
Silencing of the Charcot-Marie-Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells
Alexandre Chojnowski et al.
NEUROBIOLOGY OF DISEASE (2007)
Nuclear translocation of EndoG at the initiation of disuse muscle atrophy and apoptosis is specific to myonuclei
Esther E. Dupont-Versteegden et al.
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY (2006)
A WD-FYVE protein binds to the kinases Akt and PKCζ/λ
Thorsten Fritzius et al.
BIOCHEMICAL JOURNAL (2006)
Myotubularin phosphatases: policing 3-phosphoinositides
Fred L. Robinson et al.
TRENDS IN CELL BIOLOGY (2006)
PtdIns(5)P activates the host cell PI3-kinase/Akt pathway during Shigella flexneri infection
C Pendaries et al.
EMBO JOURNAL (2006)
Phosphatidylinositol 3-phosphate indirectly activates KCa3.1 via 14 amino acids in the carboxy terminus of KCa3.1
S Srivastava et al.
MOLECULAR BIOLOGY OF THE CELL (2006)
The class II phosphoinositide 3-kinase PI3K-C2β regulates cell migration by a PtdIns(3)P dependent mechanism
J Domin et al.
JOURNAL OF CELLULAR PHYSIOLOGY (2005)
Sensitized RNAi screen of human kinases and phosphatases identifies new regulators of apoptosis and chemoresistance
JP MacKeigan et al.
NATURE CELL BIOLOGY (2005)
The phosphatidylinositol 3-phosphate phosphatase myotubularin-related protein 6 (MTMR6) is a negative regulator of the Ca2+-Activated K+ channel KCa3.1
S Srivastava et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex
DD Sarbassov et al.
SCIENCE (2005)
Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy
M Sandri et al.
CELL (2004)
Production of phosphatidylinositol 5-phosphate by the phosphoinositide 3-phosphatase myotubularin in mammalian cells
H Tronchère et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma
H Azzedine et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15
J Senderek et al.
HUMAN MOLECULAR GENETICS (2003)
The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice
A Buj-Bello et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Myotubularin and MTMR2, phosphatidylinositol 3-phosphatases mutated in myotubular myopathy and type 4B Charcot-Marie-Tooth disease
SA Kim et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Diagnosis of X-linked myotubular myopathy by detection of myotubularin
J Laporte et al.
ANNALS OF NEUROLOGY (2001)
Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathway
F Blondeau et al.
HUMAN MOLECULAR GENETICS (2000)
Localization of phosphatidylinositol 3-phosphate in yeast and mammalian cells
DJ Gillooly et al.
EMBO JOURNAL (2000)
Myotubularin, a protein tyrosine phosphatase mutated in myotubular myopathy, dephosphorylates the lipid second messenger, phosphatidylinositol 3-phosphate
GS Taylor et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2
A Bolino et al.
NATURE GENETICS (2000)
Share Paper
