Genetic mutation - Globe Thesis

Keyword [Genetic mutation] Result: 21 - 40 \| Page: 2 of 7
21.	Clinical Characteristics And Genetic Screening Of Arrhythmogenic Right Ventricular Cardiomyopathy
22.	Epidermal Growth Factor Receptor Mutations In Esophageal Adenocarcinoma And Barrett's Esophagus
23.	Mutational Analysis Of CHRNB2 Gene In The Southern Chinese ADNFLE Population
24.	Studies On The Genetic Mutation Of Spinocerebellar Ataxia Type 12 And Clinical Characteristics From A Uygur Nationality Parentage
25.	Lipid Metabolism-related Gene Mutation Mouse Model Of Atherosclerosis Mechanism
26.	Analysis Of Genetic Diversity Of HIV-1 Tat In Patients With ADC And Non-ADC And Effect Of The Diversity On The Eliciting Of TNF-Î± And IL-1Î² By U87 Cells
27.	The Structural Domain Analysis Of P53 N-terminal Transcriptional Activation Domain Interaction With Actin
28.	The Significance Of Expression And Genetic Mutation Of Cx26, Cx32 In The Pathological Skin Scar And Scar Carcinoma
29.	Roles Of Genetic Polymorphism And Mutation In Esophageal Squamous Cell Carcinoma (ESCC) And Non-small Cell Lung Cancer (NSCLC)
30.	The Role Of RAS Mutation And PHLPP1in Myeloid Leukemia
31.	Towards Personalized Medicine Of Hepatitis B Virus Infectious Disease Based On Genetic Mutation Detection And Analysis
32.	Studies On Mutations Of Deafness Causative Genes In Children Aged0ï½ž7Years From Part Of Northwest China
33.	Studies On The Genetic Mutation, Microstructure Damage Imaging Characteristics On White Matter Brain, Serum Î±-Synuclein Expression Level Of Spinocerebellar Ataxia Type12
34.	Clinical And Molecular Genetic Features Of Adult Mixed Phenotype Acute Leukemia
35.	The Prevalence And Characteristics Of Drug Resistant Tuberculosis In Shandong Province
36.	Clinical Evaluation Of Laporoscopic Surgery For Children With Persistent Cloaca And Whole-exome Sequencing Screen In Human Persistent Cloaca
37.	A Research On The Relativity Between Clinical Characteristics Of Leber Hereditary Optic Neuropathy And Genetic Mutation
38.	An Exploratory Study On Surfactant Protein B(SP-B) Hereditary Deficiency Of Neonatal Respiratory Distress Syndrome In Full Term Infant
39.	The Research On NAChR Gene And CSNP Of Chinese Patients With ADNFLE
40.	A Study On The Mutations Of ARIDIA Gene And The Correlation Of ARID1A And ER, PR, P53mRNA In The Endometrial Carcinoma Cell Lines
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