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Keyword [Deletion]
Result: 181 - 200 | Page: 10 of 10
181. Predicting Of Radiosensitivity Of Human Tumor Cell Lines In Vitro By Determining 4977bp Deletion In Mitochondrial DNA
182. Intravenous Thrombolysis By Tissue-type Plasminogen Activator Deletion Mutant In A Rabbit Model Of Retinal Artery Occlusion
183. The Effect Of Deletion Mutant △IPS-1 To IFN-β Induction And Its Antiviral To HSV-1
184. The Study On The Deletion Of Exons And Protein Expression Of Rap1GAP, And Its Relationship With The Expression Of MMP2 And MMP9 In Invasive Breast Cancer
185. Mutational Analysis Of Glutamate Receptor Delta 2 Gene (GluR δ2) In Patients With Cerebellar Ataxia
186. Mitochondrial DNA 4977 Bp Deletion And Content In Diminished Ovarian Reserve Patients' Unfertilized Oocytes
187. Research Of Diminished Ovarian Reserve For The Copy Number And Deletion Of 4977bp Of Granular Cell Mitochondria DNA
188. Deletion Of P15 Gene And Promoter Methylation In Myelodysplastic Syndromes
189. Analysis Of The 14 Bp Insertion/deletion Polymorphism In Human Leukocyte Antigen-G Gene In Chinese Han, Bulang, Dai And Hani Ethnic Groups In Yunan Province
190. The Relationship Between Insertion/Deletion Polymorphism Of Angiotensin-Converting Enzyme Gene And Cerebrovascular Diseases Of Naxi Populations
191. The Study On The Association Of Multiple Sclerosis With Nogo 3'UTR CAA Insertion/Deletion Polymorphism
192. The Role Of Sp1 Binding Element In Regulation Of RIP2 Gene
193. Parkin Deletion And Meis1 P. R272H Mutation Analysis Of A Restless Legs Syndrome/Parkinson's Disease Pedigree
194. A Preliminary Study On The Correlation Of Deletion Of Chronosome 13 And Gene P53 With Multiple Myeloma
195. Establishing A Mouse Strain Of Specific Deletion Of Smad4 In Smooth Muscle Cells
196. Diagnosis Of A Patient With MCD Deficiency By Cytogenetic And Multiple Molecular Genetic Techniques
197. The Clinical Significance Of TP53 Deletion In Acute Leukemia Patients With Complex Chromosomal Abnormalities
198. Modeling And Simulation Of Associative Memory Dysfunction Of Hippocampal CA3 Region With Hopfield-like Network
199. Identification Of The De Novo Mutation At The α2-globin Gene And SEA Type Of α-thalassmia Deletion Causing Hemoglobin H Disease
200. Clinical Observation On Treatment Of Azoospermia Due To DAZ Gene Deletion With Yangjing Capsule
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