スポンサーリンク
International Research And Educational Institute For Integrated Medical Sciences (ireiims) Tokyo Wom | 論文
- Effects of the PPARγ activator pioglitazone on p38 MAP kinase and IκBα in the spinal cord of a transgenic mouse model of amyotrophic lateral sclerosis
- Protein-bound crotonaldehyde accumulates in the spinal cord of superoxide dismutase-1 mutation-associated familial amyotrophic lateral sclerosis and its transgenic mouse model
- Intracellular binding of fukutin and α-dystroglycan : Relation to glycosylation of α-dystroglycan
- WS1-3 Accumulation of protein-bound crotonaldehyde in the spinal cord of a transgenic mouse model of amyotrophic lateral sclerosis(THE 46TH ANNUAL MEETING OF THE JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY)
- Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy
- Unique astrocytic inclusion in a 2 month-old baby showing Leigh-like brain lesions with lactic acidosis
- P-39 Continuous expression of c-jun and c-fos oncogene in developmental stage of rat brain
- Early stage of human adenovirus type 12-inoculated retinal tissue of F344 newborn rat
- PJ-735 The Same Mutations in the Cardiac Troponin T Gene Show Various Prognoses in Japanese Patients with Hypertrophic Cardiomyopathy(Cardiac hypertrophy, basic/clinical-4 (M) PJ125,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting
- Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy
- Fukuyama congenital muscular dystrophy: Cortical dysplasia of the cerebrum in a 20 week fetus
- Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications
- Fukutin expression in mouse non-muscle somatic organs : its relationship to the hypoglycosylation of α-dystroglycan in Fukuyama-type congenital muscular dystrophy
- S3-8 Expression and localization of fukutin, POMGnT1 , POMT1 in the central nervous tissue without non-neuromuscular diseases(THE JOINT MEETING OF THE 44TH ANNUAL MEETING OF THE JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY AND THE 35TH ANNUAL MEETING
- Comparison of protein behavior between wild-type and G601S hERG in living cells by fluorescence correlation spectroscopy
- Congenital Cardiovascular Diseases and a Trial of the Integrated System of Treatment(Morning Lecture 11 (ML11) (M),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart Defects
- A functional analysis of GABARAP on 17p13.1 by knockdown zebrafish
- Soluble ST2 and N-terminal pro-Brain Natriuretic Peptide Combination:– Useful Biomarker for Predicting Outcome of Childhood Pulmonary Arterial Hypertension –