Lv3
250 积分 2023-08-23 加入
A Machine Learning Algorithm Facilitates Prognosis Prediction and Treatment Selection for Barcelona Clinic Liver Cancer Stage C Hepatocellular Carcinoma
5个月前
已完结
Two‐Step Machine Learning Model Enhances Identification of High‐Risk Metabolic Dysfunction‐Associated Steatotic Liver Disease
5个月前
已完结
Anatomic Lung Resection Is Associated With Improved Survival Compared With Wedge Resection for Stage IA (≤2 cm) NSCLC
5个月前
已完结
Gait Analysis in Neurologic Disorders
8个月前
已完结
Development and Validation of a Predictive Model for Early Identification of Cognitive Impairment Risk in Community-Based Hypertensive Patients
9个月前
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
9个月前
已完结
Stimuli-responsive ferroptosis for cancer therapy
9个月前
已完结
Association Between Plant-Based Dietary Patterns and the Long-Term Trajectory of Depressive Symptoms: A 10-Year Longitudinal Study
10个月前
已完结
Immune checkpoint inhibitors in hepatocellular carcinoma: emerging challenges in clinical practice
10个月前
已完结
Cytoreductive surgery and HIPEC with oxaliplatin for the treatment of peritoneal carcinomatosis from recurrent fibrolamellar carcinoma
10个月前
已关闭
Genotype & phenotype in Lowe Syndrome: specificOCRL1patient mutations differentially impact cellular phenotypes
8个月前
已采纳
An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population
8个月前
已采纳
RERE deficiency contributes to the development of orofacial clefts in humans and mice
8个月前
已采纳
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease
8个月前
已采纳
De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype–phenotype correlations
8个月前
已采纳
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans
8个月前
已采纳
Hypermethylation in the promoter regions of flavonoid pathway genes is associated with skin color fading during ‘Daihong’ apple fruit development
8个月前
已采纳
Compound heterozygous variants of ANKFY1 in a child with infantile-onset proteinuria and movement disorder
8个月前
已采纳
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