Related references
Note: Only part of the references are listed.Charcot-marie-tooth disease:: A clinico-genetic confrontation
N. Barisic et al.
ANNALS OF HUMAN GENETICS (2008)
Bioinformatic analyses of mammalian 5'-UTR sequence properties of mRNAs predicts alternative translation initiation sites
Jill L. Wegrzyn et al.
BMC BIOINFORMATICS (2008)
Blockade of hexokinase activity and binding to mitochondria inhibits neurite outgrowth in cultured adult rat sensory neurons
Zuocheng Wang et al.
NEUROSCIENCE LETTERS (2008)
Expression of hexokinase isoforms in the dorsal root ganglion of the adult rat and effect of experimental diabetes
Natalie J. Gardiner et al.
BRAIN RESEARCH (2007)
Mitochondrial hexokinases, novel mediators of the antiapoptotic effects of growth factors and Akt
R. B. Robey et al.
ONCOGENE (2006)
Early clinical and electrophysiologic features of the two most common autosomal recessive forms of Charcot-Marie-Tooth disease in the Roma (Gypsies)
Velina Guergueltcheva et al.
JOURNAL OF CHILD NEUROLOGY (2006)
A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes
R Gooding et al.
JOURNAL OF MEDICAL GENETICS (2005)
A newly discovered founder population: the Roma/Gypsies
L Kaaydjieva et al.
BIOESSAYS (2005)
Activated mitofusin 2 signals mitochondrial fusion, interferes with Bax activation, and reduces susceptibility to radical induced depolarization
M Neuspiel et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Krox-20 inhibits Jun-NH2-terminal kinase/c-Jun to control Schwann cell proliferation and death
DB Parkinson et al.
JOURNAL OF CELL BIOLOGY (2004)
Strengths and weaknesses of EST-based prediction of tissue-specific alternative splicing
S Gupta et al.
BMC GENOMICS (2004)
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome
R Varon et al.
NATURE GENETICS (2003)
Local regulation of fat metabolism in peripheral nerves
MHG Verheijen et al.
GENES & DEVELOPMENT (2003)
The translation of an antiapoptotic protein HIAP2 is regulated by an upstream open reading frame
D Warnakulasuriyarachchi et al.
CELL DEATH AND DIFFERENTIATION (2003)
Isozymes of mammalian hexokinase: structure, subcellular localization and metabolic function
JE Wilson
JOURNAL OF EXPERIMENTAL BIOLOGY (2003)
Refined mapping of the HMSNR critical gene region-construction of a high-density integrated genetic and physical map
J Hantke et al.
NEUROMUSCULAR DISORDERS (2003)
HK Utrecht: missense mutation in the active site of human hexokinase associated with hexokinase deficiency and severe nonspherocytic hemolytic anemia
R van Wijk et al.
BLOOD (2003)
Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A
S Sancho et al.
BRAIN (2001)
Hereditary motor and sensory neuropathy-Russe: New autosomal recessive neuropathy in Balkan gypsies
PK Thomas et al.
ANNALS OF NEUROLOGY (2001)
Structure of the 5′ region of the human hexokinase type I (HKI) gene and identification of an additional testis-specific HKI mRNA
F Andreoni et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION (2000)
Hsp27 negatively regulates cell death by interacting with cytochrome c
JM Bruey et al.
NATURE CELL BIOLOGY (2000)
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom
L Kalaydjieva et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Negative and translation termination-dependent positive control of FLI-1 protein synthesis by conserved overlapping 5′ upstream open reading frames in Fli-1 mRNA
S Sarrazin et al.
MOLECULAR AND CELLULAR BIOLOGY (2000)
A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23
T Rogers et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Share Paper
