point mutation - Globe Thesis

Keyword [point mutation] Result: 121 - 140 \| Page: 7 of 8
121.	The Effect Of Auranofin And Polymyxin Combined With Vorinostat Against Multidrug-resistant Gram-negative Bacteria And The Resistance Mechanism Of Auranofin
122.	Molecular Detection Of Spinal Muscular Atrophy By MALDI-TOF MS&Preimplantation Genetic Diagnosis Of ?-thalassemia SEA Deletion Utilizing Whole Genome Amplification And Short Fragment Gap-PCR Method
123.	Correlation Between HBX Site Mutations And Serum VEGF-C,VEGF-D Expression In Patients With Hepatitis B-related Hepatocellular Carcinoma
124.	Role Of P429R,a Point Mutation Of DGCR2 Related To Schizophrenia
125.	The Correlation Between Mitochondrial DNA Variation And Acute Mountain Sickness In Young Han Males
126.	Drug Resistance And Mechanism Of Azithromycin Resistance In Neisseria Gonorrhoeae Isolates
127.	Role Of Different Point Mutations Of FAM20C On Osteoblasts And Odontoblasts Behavioral Research
128.	The Study On The Structure Of Hepatitis C Virus Core G-Guadruplex Structure And Its Protein Expresssion And Immunosuppression
129.	Identification Of Pathogenic Point Mutations In Spinal Muscular Atrophy And Embryonic Therapy In SMA Mouse Using CRISPR/Cas9
130.	Establishment Of IKBKB Point Mutation Mouse Model And Preliminary Study Of Immunological Phenotype And Neutrophil Function And Clinical And Immunological Characteristics Of A Case With IFIH1 Mutation
131.	Sensitive,Enzyme-free And Label-free Electrochemical Sensor For K-ras G12D Point Mutation Detection
132.	Construction Of PLC?2(S707Y) Point Mutation And Sp110 Knockout Mouse Model By CRISPR/Cas9 Technology And The Analysis Of PLC?2(S707Y) Point Mutant Mouse
133.	Point Mutation Screening Of Tumour Neoantigens And Induced Specific CTLs Using The Cancer Genome Atlas Database
134.	The VAPB Point Mutation Associated With Amyotrophic Lateral Sclerosis Can Affect Myoblast Differentiation Through The IGF1-AKT Signaling Pathway
135.	Preparation And Research For Immunogenicity Of Low Activity Human Tumor Necrosis Factor
136.	The CRISPR/Cas9 System-mediated Gene Knock-in Was Used To Construct A Mouse Model Of Hepatolenticular Degeneration Of Type R778L
137.	In Vivo Point Mutation Repair: The Sickle Cell Allele as a Demonstration Case
138.	Development of Protein-Catalyzed Capture (PCC) Agents with Application to the Specific Targeting of the E17K Point Mutation of Akt1
139.	SENP7-mediated AQP4 DeSUMOylation Induces Golgiphagy To Promote Cardiac Hypertrophy By Apelin-13/APJ System
140.	The Effects Of Mucosal Adjuvant On FimH And Its Variants
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