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Keyword [Knock-in mouse model]
Result: 1 - 15 | Page: 1 of 1
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 Dhtkd1
Tyr486*
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 Skp2
G72S/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 Dhtkd1
Tyr486*
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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