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iPS細胞使った網膜を難病患者に移植へ 臨床研究を申請 (NHK)

重い目の病気である「網膜色素変性症」という難病の患者を対象に、iPS細胞を使った新たな臨床研究を行う計画を神戸市の眼科医療施設などが専門の委員会に申請したと公表...

  1. 入院患者18人 特定の抗生物質が効かない...
  2. 新規診断多発性骨髄腫患者に対する導入療法...
  3. 70歳以上の再発・難治性低悪性度非ホジキ...
  4. 若年成人FLT3/ITD変異陽性AMLへ...

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「glucocerebrosidase」の検索結果

3010件中 41件~60件表示    検索結果をPubMedで見る PubMedで見る

Glucocerebrosidase and its relevance to Parkinson disease.

Ambroxol Hydrochloride Improves Motor Functions and Extends Survival in a Mouse Model of Familial Amyotrophic Lateral Sclerosis.

Gaucher disease in Montenegro - genotype/phenotype correlations: Five cases report.

Lipids as -Acting Effectors for α-Synuclein in the Pathogenesis of Parkinson's Disease.

Differential Isotope Labeling by Permethylation and Reversed-Phase Liquid Chromatography-Mass Spectrometry for Relative Quantification of Intact Neutral Glycolipids in Mammalian Cells.

Gene expression in stress urinary incontinence: a systematic review.

Age-related neurochemical and behavioural changes in D409V/WT GBA1 mouse: Relevance to lewy body dementia.

Progranulin deficiency leads to reduced glucocerebrosidase activity.

Imaging of non-neuronopathic Gaucher disease: recent advances in quantitative imaging and comprehensive assessment of disease involvement.

Can GBA1-Associated Parkinson Disease Be Modeled in the Mouse?

The Link between Gaucher Disease and Parkinson's Disease Sheds Light on Old and Novel Disorders of Sphingolipid Metabolism.

Lessons on Differential Neuronal-Death-Vulnerability from Familial Cases of Parkinson's and Alzheimer's Diseases.

Evolution and clustering of prodromal parkinsonian features in GBA1 carriers.

Viral delivery of a microRNA to Gba to the mouse central nervous system models neuronopathic Gaucher disease.

Scaffolds for Sustained Release of Ambroxol Hydrochloride, a Pharmacological Chaperone That Increases the Activity of Misfolded β-Glucocerebrosidase.

Evolution of prodromal parkinsonian features in a cohort of mutation-positive individuals: a 6-year longitudinal study.

A Neonatal Case With Perinatal Lethal Gaucher Disease Associated With Missense G234E and H413P Heterozygous Mutations.

Gaucher Disease Involving Virchow's Lymph Node: a Case Report.

GBA1-associated parkinsonism: new insights and therapeutic opportunities.

Synthesis of modified 1,5-imino-d-xylitols as ligands for lysosomal -glucocerebrosidase.

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