Lv71
4900 积分 2023-03-14 加入
MUC17 mutations and methylation are associated with poor prognosis in adult-type diffuse glioma patients
27天前
已完结
The pan-cancer proteome atlas, a mass spectrometry-based landscape for discovering tumor biology, biomarkers, and therapeutic targets
1个月前
已完结
MUC17 mutations and methylation are associated with poor prognosis in adult-type diffuse glioma patients
1个月前
已完结
The proteomic skin profile of moderate-to-severe atopic dermatitis patients shows an inflammatory signature
2个月前
已关闭
The proteomic skin profile of moderate-to-severe atopic dermatitis patients shows an inflammatory signature
2个月前
已关闭
Abrocitinib versus dupilumab: Impact on skin barrier function and proteomics in atopic dermatitis
2个月前
已完结
Developmental Localization of the Splicing Alternatives of Fibroblast Growth Factor Receptor-2 (FGFR2)
4个月前
已完结
The proteomic skin profile of moderate-to-severe atopic dermatitis patients shows an inflammatory signature
4个月前
已关闭
RORγt eTACs mediate oral tolerance and Treg induction
5个月前
已完结
CCR8: a promising therapeutic target against tumor-infiltrating regulatory T cells
5个月前
已完结
Comparative single-cell and spatial profiling of anti-SSA-positive and anti-centromere-positive Sjögren’s disease reveals common and distinct immune activation and fibroblast-mediated inflammation
8个月前
已采纳
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements
8个月前
已采纳
Accurate formation enthalpies of solids using reaction networks
8个月前
已采纳
Proximal cooperative aerial manipulation with vertically stacked drones
8个月前
已采纳
Molecular diagnosis and novel genes and phenotypes in a pediatric thoracic insufficiency cohort
8个月前
已采纳
Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse
8个月前
已采纳
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model
8个月前
已采纳
Conserve marine migratory species to protect ecological links between land and sea
8个月前
已采纳
Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformation
8个月前
已采纳
Overlooked KCNQ4 variants augment the risk of hearing loss
8个月前
已采纳
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