Lv3
280 积分 2023-08-23 加入
Gait Analysis in Neurologic Disorders
2天前
已完结
Development and Validation of a Predictive Model for Early Identification of Cognitive Impairment Risk in Community-Based Hypertensive Patients
21天前
已完结
The rising tide of early-onset colorectal cancer: a comprehensive review of epidemiology, clinical features, biology, risk factors, prevention, and early detection
24天前
已完结
Stimuli-responsive ferroptosis for cancer therapy
25天前
已完结
Association Between Plant-Based Dietary Patterns and the Long-Term Trajectory of Depressive Symptoms: A 10-Year Longitudinal Study
1个月前
已完结
Immune checkpoint inhibitors in hepatocellular carcinoma: emerging challenges in clinical practice
1个月前
已完结
Cytoreductive surgery and HIPEC with oxaliplatin for the treatment of peritoneal carcinomatosis from recurrent fibrolamellar carcinoma
1个月前
已关闭
Management of Hepatocellular Carcinoma
2个月前
已完结
NAT10 Drives Cisplatin Chemoresistance by Enhancing ac4C-Associated DNA Repair in Bladder Cancer
3个月前
已完结
Development and Validation of a Nutritional Frailty Phenotype for Older Adults Based on Risk Prediction Model: Results from a Population-Based Prospective Cohort Study
4个月前
已完结
Genotype & phenotype in Lowe Syndrome: specificOCRL1patient mutations differentially impact cellular phenotypes
2天前
已采纳
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population
2天前
已采纳
RERE deficiency contributes to the development of orofacial clefts in humans and mice
2天前
已采纳
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease
2天前
已采纳
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype–phenotype correlations
2天前
已采纳
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans
2天前
已采纳
Hypermethylation in the promoter regions of flavonoid pathway genes is associated with skin color fading during ‘Daihong’ apple fruit development
2天前
已采纳
Compound heterozygous variants of ANKFY1 in a child with infantile-onset proteinuria and movement disorder
2天前
已采纳
Illuminating mitochondrial translation through mouse models
6个月前
已采纳
De novo non-synonymous CTR9 variants are associated with motor delay and macrocephaly: human genetic and zebrafish experimental evidence
6个月前
已采纳
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