Font Size: a A A
Keyword [Next-generation Sequencing]
Result: 61 - 80 | Page: 4 of 10
61. Characterization Of MiRNA-483-5p And Targeted Gene ERK1 In Theregulation Of Proliferation-apoptosis Balance Of Granulosa Cells And Development Of PCOS
62. Results Analysis Of Targeted Next Generation Sequencing In Patients With Unknown Intellectual/Developmental Disabilities
63. Design And Realization On The Analysis Pipeline For Mendelian Disorders Based On Next-genenration Sequencing Data
64. The Study Of Mutations In A Family Of Hereditary Spastic Paraplegia Based On The Next Generation Sequencing
65. Identification Of The Causative Genes For A Chinese Family With Autosomal Dominant Hereditary Hearing Loss And A Sporadic Case Of Usher Syndrome
66. Next-generation Sequencing And Molecular Analysis Of 3 Unexplained Intellectual Disability Patients
67. Molecular Genetic Diagnosis On Clinical Diagnostic Assessments That Demonstrate Correlations In Patients With Autosomal Recessive Inherited Retinal Dystrophies
68. A New Method To Detect α-thalassemia Deletions Using Nextgeneration Sequencing
69. Predicting The Curative Effect Of Neoadjuvant Chemotherapy With Multiple Pathways Genes In Breast Cancer
70. Variation Detection Based On Next-generation Sequencing Of Type Chinese 1 Strains Of Toxoplasma Gondii With Different Virulence From China
71. Identification Of Driver Genes And Pathways In Cancer With Omics Data Based On High-throughput Sequencing
72. A Murine Asthma Model Of DOCK8 Knockout Mice:More Susceptible To Airway Allergy And The Mechanism Of Allergic Inflammation And Clinical And Immunological Analysis Of A Patient With SCID Due To CD3ε Deficiency
73. Genetic Stability Of Sabin Strain As Virus Seed For Production Of Inactivated Poliomyelitis Vaccine And Deep Sequencing Method Of Sabin Strain Virus
74. Accurate Detection For Hemoglobin Variants Of Thalassemia Based On Next Generation Sequencing Target Capture Technology
75. The Mining And Validation Of MiRNA Biomakers In Diffuse Large B Cell Lymphoma
76. Genetic Diagnosis Of Congenital Cateracts Using Target Enrichment Technology And Function Characterization Of Disease-causative Mutation(EPHA2 P.G668D)
77. The Application Of 189-Target Capture Chip In Hereditary Retinal Diseases
78. The Features Of T Cell Clones And Regulation Of Vascular Endothelial Function By Let-7e In Atherosclerotic Lesions
79. Establishment And Clinical Application Of Preimplantation Genetic Diagnosis Technique Platform For ?eta-thalassemia In Guangxi Area
80. Genetic Diagnosis And Clinical Characterization Of Familial Renal Glucosuria
  <<First  <Prev  Next>  Last>>  Jump to