A5079678496- Nanoplatforms for cancer theranostics
- Nanoparticle-Based Drug Delivery
- Pediatric Hepatobiliary Diseases and Treatments
- Head and Neck Anomalies
- Thyroid and Parathyroid Surgery
- Perovskite Materials and Applications
- Radiation Therapy and Dosimetry
- Neurogenetic and Muscular Disorders Research
- Thyroid Cancer Diagnosis and Treatment
- Neonatal Health and Biochemistry
- Metabolism and Genetic Disorders
- Genetics and Neurodevelopmental Disorders
- Extracellular vesicles in disease
- Amino Acid Enzymes and Metabolism
Changchun University of Chinese Medicine
2022-2023
The Affiliated Hospital to Changchun University of Chinese Medicine
2023
Union Hospital
2019-2020
Jilin University
2019-2020
Union Hospital
2020
The advantages of PCM@Lip/IT NPs include mitochondrial-targeting, on-demand drug release, and prodrug activation by hypoxia with guidance/monitoring PA FL imaging.
Introduction: Citrin is a calcium-bound aspartate-glutamate carrier protein encoded by the gene SLC25A13, mutations of which can cause citrin deficiency, an autosomal recessive disorder. The manifestations deficiency include neonatal intrahepatic choledeposits caused (NICCD: OMIM#605814), intermediate growth disorders and dyslipidemia citrullinemia type II (OMIM#603471) in adults. NICCD classical metabolic disorder that causes cholestasis newborns. Patient concern clinical findings: Here, we...
The VPS33B (OMIM: 608552) gene is located on chromosome 15q26.1. We found a female infant with autosomal recessive arthrogryposis, renal dysfunction and cholestasis syndrome 1 (ARCS1) caused by mutation in VPS33B. child was diagnosed ARCS1 208085) after the whole exome sequencing revealed two heterozygous mutations (c.96+1G>C, c.242delT) gene.We report Chinese neonatal disorder, who eventually genetic analysis. Genetic testing new (c.96+1G>C VPS33B, which causal gene. patient compound...