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Chiara Fallerini

University of Siena
H指数:32
被引数:7,137

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Trop-1/EpCAM Thr115 is a driver of hyperproliferative cell repair and of severe lung damage in COVID-19

Trop-1/EpCAM Thr115是COVID-19中细胞过度增殖修复和严重肺损伤的驱动因素

2026-09-010
OAAI
A comprehensive European Colorectal Cancer Cohort dataset

一个全面的欧洲结直肠癌队列数据集

2026-03-120
OAAI
A Complex Case of Retinoblastoma Solved by the Combined Approach of Humor/Plasma cfDNA-NGS and LR-WGS

视网膜母细胞瘤的复杂病例通过Humor/Plasma cfDNA-NGS与LR-WGS的联合方法得到解决

2025-11-220
OAAI
Validation of the NovaSeq6000 Platform and automated library preparation for CE-IVD equivalence

NovaSeq6000平台的验证及用于CE-IVD等效性的自动化文库制备

2025-11-010
OAAI
Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine response
2024-04-041
OA
CYP19A1 mediates severe SARS-CoV-2 disease outcome in males

CYP19A1介导男性严重SARS-CoV-2疾病转归

2023-09-017
OAAI
SELP Asp603Asn and severe thrombosis in COVID-19 males (vol 14, 123, 2021)
2023-02-150
OAAI
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

罕见的编码变异提供了对自闭症遗传结构和表型背景的洞察

2022-08-18198
OA
Carriers of ADAMTS13 Rare Variants Are at High Risk of Life-Threatening COVID-19
2022-05-292
OAAI
The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder
2022-04-116
OA
The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males
AUTOPHAGY
IF14.3
2021-12-2925
OAAI
Rare variants in Toll-like receptor 7 results in functional impairment and downregulation of cytokine-mediated signaling in COVID-19 patients
2021-12-2443
OAAI
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
2021-12-1026
OAAI