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ジュゴン、沖縄の2島に生息か (デイリースポーツ)

環境省は31日、絶滅の恐れが極めて高いジュゴンが海草を食べたとみられる跡を、沖縄県の伊良部島と波照間島の沿岸で初めて確認したとの調査結果を発表した。姿を捉えるこ...

  1. 演歌歌手の加門亮さん 死去 (NHK)
  2. 新型コロナウイルス感染症の患者等の発生に...
  3. 新型コロナウイルス感染症の大規模な感染拡...
  4. 新型コロナウイルス感染症の現在の状況と厚...

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「"Al-Sarraj S "[Author]」の検索結果

197件中 1件~20件表示    検索結果をPubMedで見る PubMedで見る

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.

5-ALA fluorescence in a WHO grade I papillary glioneuronal tumour: a case report.

Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates.

DNA methylation-based profiling for paediatric CNS tumour diagnosis and treatment: a population-based study.

ATRX immunohistochemistry can help refine 'not elsewhere classified' categorisation for grade II/III gliomas.

Heritability and genetic variance of dementia with Lewy bodies.

Parallel profiling of DNA methylation and hydroxymethylation highlights neuropathology-associated epigenetic variation in Alzheimer's disease.

Primum non nocere: a call for balance when reporting on CTE.

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.

Comparison of clinical and neuropathological diagnoses of neurodegenerative diseases in two centres from the Brains for Dementia Research (BDR) cohort.

Cranial vault unicameral bone cyst.

Adult parasellar capillary haemangioma with intrasellar extension.

A comprehensive screening of copy number variability in dementia with Lewy bodies.

A cross-brain regions study of ANK1 DNA methylation in different neurodegenerative diseases.

A histone acetylome-wide association study of Alzheimer's disease identifies disease-associated H3K27ac differences in the entorhinal cortex.

Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia.

Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease.

Variation at the TRIM11 locus modifies Progressive Supranuclear Palsy phenotype.

Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cells.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

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