Pages that link to "Q40045644"
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The following pages link to Hitoshi Warita (Q40045644):
Displaying 50 items.
- An inducer of VGF protects cells against ER stress-induced cell death and prolongs survival in the mutant SOD1 animal models of familial ALS (Q27312650) (← links)
- Glutamate enhances DNA fragmentation in cultured spinal motor neurons of rat. (Q32039204) (← links)
- GNE myopathy associated with congenital thrombocytopenia: a report of two siblings (Q33417862) (← links)
- Rheumatoid factor positive hypertrophic cranial pachymeningitis in association with hypopituitarism and multiple cranial nerve palsies. (Q34387269) (← links)
- Immunolocalization of corticotropin-releasing hormone (CRH) and its receptors (CRHR1 and CRHR2) in human endometrial carcinoma: CRHR1 as a potent prognostic factor. (Q34434269) (← links)
- Proteasome dysfunction induces muscle growth defects and protein aggregation. (Q34698515) (← links)
- Corticotropin-Releasing Hormone Receptor 2 Gene Variants in Irritable Bowel Syndrome (Q35903549) (← links)
- Isolated inclusion body myopathy caused by a multisystem proteinopathy-linked hnRNPA1 mutation (Q36733879) (← links)
- Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing (Q36738610) (← links)
- Establishment of In Vitro FUS-Associated Familial Amyotrophic Lateral Sclerosis Model Using Human Induced Pluripotent Stem Cells. (Q36805034) (← links)
- Multicenter questionnaire survey for sporadic inclusion body myositis in Japan (Q37400774) (← links)
- A case of McArdle disease: efficacy of vitamin B6 on fatigability and impaired glycogenolysis (Q37777937) (← links)
- Altered Tau Isoform Ratio Caused by Loss of FUS and SFPQ Function Leads to FTLD-like Phenotypes. (Q39095704) (← links)
- Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan. (Q40045594) (← links)
- In vivo adenovirus-mediated gene transfer and expression in ischemic rabbit spinal cord (Q40798274) (← links)
- Induction of glial cell line-derived neurotrophic factor receptor proteins in cerebral cortex and striatum after permanent middle cerebral artery occlusion in rats (Q40941812) (← links)
- A novel SOD1 gene mutation in familial ALS with low penetrance in females (Q43727681) (← links)
- Expressions of nitrotyrosine and TUNEL immunoreactivities in cultured rat spinal cord neurons after exposure to glutamate, nitric oxide, or peroxynitrite (Q43728407) (← links)
- Early decrease of the immunophilin FKBP 52 in the spinal cord of a transgenic model for amyotrophic lateral sclerosis (Q44026113) (← links)
- Tardive decrease of astrocytic glutamate transporter protein in transgenic mice with ALS-linked mutant SOD1. (Q44142407) (← links)
- Ultrastructural study of mitochondria in the spinal cord of transgenic mice with a G93A mutant SOD1 gene (Q44804413) (← links)
- Slow component of axonal transport is impaired in the proximal axon of transgenic mice with a G93A mutant SOD1 gene (Q44804417) (← links)
- Expressions of caspase-3, Tunel, and Hsp72 immunoreactivities in cultured spinal cord neurons of rat after exposure to glutamate, nitric oxide, or peroxynitrite. (Q44865100) (← links)
- Intrathecal delivery of hepatocyte growth factor from amyotrophic lateral sclerosis onset suppresses disease progression in rat amyotrophic lateral sclerosis model (Q45872534) (← links)
- Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure. (Q45934258) (← links)
- Up-regulation of insulin-like growth factor-II receptor in reactive astrocytes in the spinal cord of amyotrophic lateral sclerosis transgenic rats (Q46622923) (← links)
- FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion. (Q46742950) (← links)
- ITIH4 and Gpx3 are potential biomarkers for amyotrophic lateral sclerosis. (Q46935418) (← links)
- Aberrant astrocytic expression of chondroitin sulfate proteoglycan receptors in a rat model of amyotrophic lateral sclerosis. (Q47684146) (← links)
- Topical application of neurotrophin-3 attenuates ischemic brain injury after transient middle cerebral artery occlusion in rats (Q48087870) (← links)
- Expression of cyclin-dependent kinase 5 and its activator p35 in rat brain after middle cerebral artery occlusion (Q48211479) (← links)
- Selective impairment of fast anterograde axonal transport in the peripheral nerves of asymptomatic transgenic mice with a G93A mutant SOD1 gene (Q48259447) (← links)
- FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation (Q48414675) (← links)
- Parvalbumin and calbindin D-28k immunoreactivity in transgenic mice with a G93A mutant SOD1 gene (Q48613472) (← links)
- Two cases of Japanese CADASIL with corpus callosum lesion (Q48687964) (← links)
- Nocturnal blood pressure dip in CADASIL. (Q48707344) (← links)
- Induction of PML immunoreactivity in rat brain neurons after transient middle cerebral artery occlusion (Q48730689) (← links)
- Early decrease of redox factor-1 in spinal motor neurons of presymptomatic transgenic mice with a mutant SOD1 gene (Q48771567) (← links)
- Different expression of glycogen synthase kinase-3beta between young and old rat brains after transient middle cerebral artery occlusion (Q48799928) (← links)
- Oxidative damage to mitochondrial DNA in spinal motoneurons of transgenic ALS mice (Q48908317) (← links)
- Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. (Q51153083) (← links)
- Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutation. (Q51561052) (← links)
- [Clinical translation of hepatocyte growth factor for amyotrophic lateral sclerosis]. (Q53131808) (← links)
- Accumulation of chondroitin sulfate proteoglycans in the microenvironment of spinal motor neurons in amyotrophic lateral sclerosis transgenic rats. (Q53480764) (← links)
- Effects of repeated methyl levodopa administration on apomorphine sensitivity of rotational behavior and striatal Fos expression of rats with unilateral 6-OHDA lesions. (Q53795514) (← links)
- Continuous administration of poloxamer 188 reduces overload-induced muscular atrophy in dysferlin-deficient SJL mice. (Q54341274) (← links)
- TARDBP p.G376D mutation, found in rapid progressive familial ALS, induces mislocalization of TDP-43. (Q55342247) (← links)
- Rostrocaudal Areal Patterning of Human PSC-Derived Cortical Neurons by FGF8 Signaling. (Q55401574) (← links)
- Pathomechanism and prevalence of sporadic inclusion body myositis (sIBM) (Q58036242) (← links)
- Interstitial pneumonia and other adverse events in riluzole-administered amyotrophic lateral sclerosis patients: a retrospective observational study (Q64083560) (← links)