16 results on '"Zeng, Baitao"'
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2. Identification of two novel and one rare mutation in DYRK1A and prenatal diagnoses in three Chinese families with intellectual Disability-7
3. Identification of five novel SCN1A variants
4. Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNA
5. Application of whole-exome sequencing technology in clarifying 269 cases of fetal skeletal system disorders
6. Mesenchymal stem cells derived from iPSCs expressing interleukin-24 inhibit the growth of melanoma in the tumor-bearing mouse model
7. Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi province
8. Mutation spectrum of PTS gene in patients with tetrahydrobiopterin deficiency from jiangxi province
9. Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2P497H Mutation
10. Full-Length Dystrophin Restoration via Targeted Exon Addition in DMD-Patient Specific iPSCs and Cardiomyocytes
11. An Episomal CRISPR/Cas12a System for Mediating Efficient Gene Editing
12. Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2 P497H Mutation.
13. Targeted addition of mini-dystrophin into rDNA locus of Duchenne muscular dystrophy patient-derived iPSCs
14. Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem Cells
15. Synthesis and Detecting Cancer Studies of Up-Conversion Luminescent Materials
16. The Application of Up-conversion Nanoparticles Materials in Cancer Diagnosis and Therapy
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