Related references
Note: Only part of the references are listed.Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio
Nicola Chiarelli et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2011)
Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency
Marjolijn Renard et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome
Yi-Ching Lee et al.
HUMAN MOLECULAR GENETICS (2010)
Mechanisms of emphysema in autosomal dominant cutis laxa
Qirui Hu et al.
MATRIX BIOLOGY (2010)
Protection against Hepatocyte Mitochondrial Dysfunction Delays Fibrosis Progression in Mice
Claudia Mitchell et al.
AMERICAN JOURNAL OF PATHOLOGY (2009)
Angiotensin II, mitochondria, cytoskeletal, and extracellular matrix connections: an integrating viewpoint
Elena M. V. de Cavanagh et al.
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY (2009)
Mutations in the SLC2A10 gene cause arterial abnormalities in mice
Chao-Hung Cheng et al.
CARDIOVASCULAR RESEARCH (2009)
TGF-beta signaling in vascular biology and dysfunction
Marie-Jose Goumans et al.
CELL RESEARCH (2009)
Mutations in PYCR1 cause cutis laxa with progeroid features
Bruno Reversade et al.
NATURE GENETICS (2009)
Molecular mechanisms of mTOR-mediated translational control
Xiaoju Max Ma et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2009)
Critical Early Roles for col27a1a and col27a1b in Zebrafish Notochord Morphogenesis, Vertebral Mineralization and Post-embryonic Axial Growth
Helena E. Christiansen et al.
PLOS ONE (2009)
ALK5- and TGFBR2-independent role of ALK1 in the pathogenesis of hereditary hemorrhagic telangiectasia type 2
Sung O. Park et al.
BLOOD (2008)
Characterization of housekeeping genes in zebrafish: male-female differences and effects of tissue type, developmental stage and chemical treatment
Amy T. McCurley et al.
BMC MOLECULAR BIOLOGY (2008)
Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions
B. L. Callewaert et al.
GENESIS (2008)
Arterial tortuosity syndrome: Clinical and molecular findings in 12 newly identified families
B. L. Callewaert et al.
HUMAN MUTATION (2008)
Oxidative stress mediates cardiac fibrosis by enhancing transforming growth factor-beta1 in hypertensive rats
Wenyuan Zhao et al.
MOLECULAR AND CELLULAR BIOCHEMISTRY (2008)
Modeling cardiovascular disease in the zebrafish
Timothy J. A. Chico et al.
TRENDS IN CARDIOVASCULAR MEDICINE (2008)
Myofibroblast contraction activates latent TGF-β1 from the extracellular matrix
Pierre-Jean Wipff et al.
JOURNAL OF CELL BIOLOGY (2007)
Compensatory signalling induced in the yolk sac vasculature by deletion of TGFβ receptors in mice
Rita L. C. Carvalho et al.
JOURNAL OF CELL SCIENCE (2007)
Clustal W and clustal X version 2.0
M. A. Larkin et al.
BIOINFORMATICS (2007)
Angiotensin II type 1 receptor blockade attenuates TGF-β-induced failure of muscle regeneration in multiple myopathic states
Ronald D. Cohn et al.
NATURE MEDICINE (2007)
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
Jan Hellemans et al.
GENOME BIOLOGY (2007)
Small molecule screening in the zebrafish
R. D. Murphey et al.
METHODS (2006)
The chondrocyte: Biology and clinical application
Zhen Lin et al.
TISSUE ENGINEERING (2006)
Fibulin-4:: A novel gene for an autosomal recessive cutis laxa syndrome
Vishwanathan Hucthagowder et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Contribution of reactive oxygen species to the pathogenesis of left ventricular failure in Dahl salt-sensitive hypertensive rats: effects of angiotensin II blockade
Peng Guo et al.
JOURNAL OF HYPERTENSION (2006)
Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome
JP Habashi et al.
SCIENCE (2006)
Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome
PJ Coucke et al.
NATURE GENETICS (2006)
Dihydropyrrolopyrazole transforming growth factor-β type I receptor kinase domain inhibitors:: A novel benzimidazole series with selectivity versus transforming growth factor-β type II receptor kinase and mixed lineage kinase-7
HY Li et al.
JOURNAL OF MEDICINAL CHEMISTRY (2006)
TGFβ pathobiology in the eye
S Saika
LABORATORY INVESTIGATION (2006)
Emerging roles for TGF-β1 in nervous system development
FCA Gomes et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2005)
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
BL Loeys et al.
NATURE GENETICS (2005)
Inflammatory cytokines and postmyocardial infarction remodeling
M Nian et al.
CIRCULATION RESEARCH (2004)
Successful shape-based virtual screening:: The discovery of a potent inhibitor of the type I TGFβ receptor kinase (TβRI)
J Singh et al.
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2003)
Dysregulation of TGF-β activation contributes to pathogenesis in Marfan syndrome
ER Neptune et al.
NATURE GENETICS (2003)
Development - Organogenesis - Heart and wood formation from the zebrafish point of view
C Thisse et al.
SCIENCE (2002)
The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members
HG Joost et al.
MOLECULAR MEMBRANE BIOLOGY (2001)
Sequence and functional analysis of GLUT10: A glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1
PA Dawson et al.
MOLECULAR GENETICS AND METABOLISM (2001)
Share Paper
