PCR mutation - Globe Thesis

Keyword [PCR mutation] Result: 1 - 18 \| Page: 1 of 1
1.	E.coli-Based Production Of Reconbinant FALL-39 And PCR-based Site-specific Mutagensis And Their Biologic Activities
2.	Study On The Mitochondrial DNA Mutations In Tumor Tissues And Peripheral Lymphocytes Of Laryngeal Squamous Cell Carcinoma
3.	Identification Of A Novel β Thalassemia Mutation And Development Of A Method For High-throughput Mutation Detection Of β-globin Gene
4.	Deficient Expression Of The Transcription Factor Sp3 In Peripheral Blood Mononuclear Cells In Multiple Sclerosis Patients And Exploration Of Its Influencing Factors
5.	Effect On Gene Expression Profiles Caused By A39S Mutated DJ-1 Protein And The Research On Detection Of DJ-1 Mutations And Serum DJ-1 Protein Concentration
6.	Study Of The Spectrum Of Febrile Seizures Related Epilepsy And Its Possible Genetics
7.	Autism In Febrile Seizures Related Epilepsy: Prevalence, Features, And Relationship To The Clinical Characteristics Of Epilepsy, Mental Retardation And SCN1A Mutation
8.	Construction, Expression And Identification Of G Protein Polypeptide Of Human Respiratory Syncytial Virus Expressed By Recombinant Adenoviruses
9.	Association Study Between COL1A1 Gene And Idiopathic Congenital Talipes Equinovarus
10.	Identification And Quantitative Assay For JAK2V617F Mutation In Patients With Myeloproliferative Neoplasms
11.	The Expression Of PIK3CA, AKT1/2 And PTEN In Hunman Colorectal Cancer And Its Clinical Significance
12.	Clinical Features And Gene Analysis In Chinese Patients With Isolate Early-Onset Parkinsonism
13.	Tumor Suppressor Gene P33 ~ (ing1) Expression And Mutation In Colorectal Cancer Study
14.	Detection Of Mutations And Expression Changes Of IDH1and IDH2in Colorectal Neoplasms
15.	Application Of Combining Direct Sequencing And CNV Detection Technology In Waardenburg Syndrome-related Genes Screening
16.	Correlation Of CT Perfusion Parameters With EGFR And MMP-9in NSCLC
17.	Gene Mutation Analysis In Chinese Patient With Hereditary Spherocytosis
18.	Detetion And Clinical Significance Of JAK2V617F Mutation In 92 Patients With Chronic Myeloproliferative Neoplasm
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