minigene - Globe Thesis

Keyword [minigene] Result: 1 - 20 \| Page: 1 of 2
1.	The Effects Of Human 21.5kDa MBP Minigene Transfer On Cell Proliferation And Apoptosis
2.	Screening And Functional Study Of Gene Mutations In Nodular Sclerosis And Pyogenic Sweatadenitis
3.	Construction And Immunological Activity Of Three Tandem Repeats Of Minigene DNA Vaccine Derived From Carcinoembryonic Antigen (CEA) Gene
4.	Establishment Of A Hemophilia B Transgenic Mouse Model On The Basis Of Coagulation Factor â…¨ Gene Knock-out Mouse
5.	The Impact Of SR Proteins And HnRNPA1 Splicing Factor Regulating The Alternative Splicing Of Human Glucocorticoid Receptor Exon 9
6.	The Study Of Treating RCC On The Recombinant AAV Mediated Secretive Expression Of NT4-TAT-6Ã—His-VHLÎ² Fusion Peptide
7.	Establishment Of The Minigene Method For Reporting The Alternative Splicing Of Bcl-x
8.	Mutation Identification And Functional Analysis Of Disease Gene In A Family With Congenital Cataract
9.	The Roles Of CPA1 Gene And SPINK1 Exonic Mutations In Pathogenesis Of Chronic Pancreatitis
10.	Screening And Functional Study For Splicing Mutation In Familial Hypercholesterolemia
11.	Association Of Ionotropic Glutamate Receptor Family Genes Variants With Attention-deficit/ Hyperactivity Disorder
12.	A Pilot Study On Association Between Meiosis Related Gene HFM1 Variation And Premature Ovarian Insufficiency
13.	Detection And Functional Study Of DOCK6 Gene Mutations In Adams-Oliver Syndrome
14.	Clinical Analysis And Genetic Study Of Alport Syndrome
15.	A Study Of Alport Syndrome Family In Western China And Its New Mutation In COL4A5 Gene
16.	Correlation Between Familial Renal Glucosuria Pathogenic SLC5A2 Gene And The Renal Threshold For Glucose Excretion And RNA Splicing Analysis
17.	Study On The Mechanism Of LncRNA EGOT Promoting Proliferation And Invasion In Thyroid Carcinoma
18.	Study On Pathogenicity Of Novel Exon And Intron Double Mutations In A Wiskott-aldrich Syndrome Family In Vitro
19.	Study Of Genetic Etiology Of Whole Exome Sequencing In Fetus With Ultrasound Structural Abnormal And In Family With Rare Disease
20.	A Study On The Causative Gene Of A SPG26 Family Based On Next-generation Sequencing Technology
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