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Keyword [Knock-in mouse model]
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1. Absence Of PTHrP Nuclear Localization And Carboxyl Terminus Leads To The Abnormalities Of Brain Development
2. Epidermolytic Palmoplantar Keratoderma:Genotype-Phenotype Correlation, Prenatal Genetics Diagnosis And Knock-in Mouse Model
3. Phenotypic Analysis Of Dhtkd1Tyr486* Knock-in Mouse Model And Pathogenic Mechanism Of Hereditary Protein C Deficiency
4. Phenotypic Analysis Of A Gene Mutation Knock-in Mouse Model Of Epidermolvtic Palmoplanta Keratoderma And Investigation On Mutant-specific ShRNA Therapy
5. S113R Mutation In Slc33a1 Leads To Hereditary Spastic Paraplegia And Augmented BMP Signaling In A Mouse Model
6. A Preliminary Research On The Effect Of Hereditary Spastic Paraplegia Causatave Gene SLC3A1 Missense Mutation On Mitochondria
7. A Preliminary Study Of The Pathological Phenotype And Pathogenic Mechanism Of The DSG2 F536C Knock-In Mouse Model
8. Establishment And Phenotype Analysis Of Skp2G72S/G72S Knock-in Mouse Model
9. Study On The Molecular Mechanism Of Metabolic Disorders Induced By Pathogenic Mutations In LPL Using A Knock-in Mouse Model
10. Study On The Molecular Pathogenesis And Targeted Therapy In Acute Myeloid Leukemia
11. Using CRISPR/Cas9 Technology To Establish An In Situ Knock-in Mouse Model Of Huntington’s Disease (HD)
12. Study On Dhtkd1Tyr486* Knock-in Mouse Model And Gene Diagnosis Of A Cone-Rod Dystrophy Family
13. The Mechanism Study Of Masseter Loss Phenotype In Mouse Model Of Fgf8 Specific Activation In Mandible-masseter Tendon
14. The Construction And Phenotypic Study Of A Novel Humanized ATXN3 Knock-in Mouse Model Using CRISPR/Cas9
15. Study On Auditory Function Of Ifnlr1 Variant Knock-In Mouse Model And Identification Of New Pathogenic Variant Of FOXC1 Gene
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