443 results on '"Lin, Shu-Wha"'
Search Results
102. Genetic Profiling in Childhood T-Cell Acute Lymphoblastic Leukemia By Targeted Sequencing
103. Functional and structural deficits of the dentate gyrus network coincide with emerging spontaneous seizures in an Scn1a mutant Dravet Syndrome model during development
104. Development of a pretreatment strategy to enhance the efficiency of hepatocyte transplantation in mice
105. A Report for Applying CRISPR/Cas9 Genome Editing Technologies on Mouse Zygotes from Taiwan Transgenic Mouse Model Core Facility (TMMC)
106. High Salt Induces Developmental Defect during Pregnancy
107. Sun1 deficiency leads to cerebellar ataxia in mice
108. The role of serine protease in the respiratory development (834.12)
109. The roles of thromboxane A 2 in high salt‐induced defect during pregnancy (832.4)
110. A Nucleolus-Predominant piggyBac Transposase, NP-mPB, Mediates Elevated Transposition Efficiency in Mammalian Cells
111. SEPT12-Microtubule Complexes Are Required for Sperm Head and Tail Formation
112. Phosphorylation Regulates NCC Stability and Transporter Activity In Vivo
113. Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated SLC26A4 Gene in Humans and Mice
114. Developing methods to enhancing cell engraftment in a genetically engineered mouse model
115. Incorporation of the factor IX Padua mutation into FIX-Triple improves clotting activity in vitro and in vivo
116. A Knock-In Npm1 Mutation in Mice Results in Myeloproliferation and Implies a Perturbation in Hematopoietic Microenvironment
117. R26R-GR: A Cre-Activable Dual Fluorescent Protein Reporter Mouse
118. Monocytic Thrombomodulin Triggers LPS- and Gram-Negative Bacteria-Induced Inflammatory Response
119. Investigation of the Dravet syndrome using a mouse model
120. Absence of biallelic TCRγ deletion predicts induction failure and poorer outcomes in childhood T-cell acute lymphoblastic leukemia
121. A “canonical” Npm1 mutation Knock-in Mouse Model Revealed Subtle but Definitive Myeloid Expansion with Poor HSC Niche Interaction
122. Impaired phosphorylation of Na + -K + -2Cl − cotransporter by oxidative stress-responsive kinase-1 deficiency manifests hypotension and Bartter-like syndrome
123. Establishment of a Knock-In Mouse Model with the SLC26A4 c.919-2A>G Mutation and Characterization of Its Pathology
124. Gene targeting and expression analysis of mouse Tem1/endosialin using a lacZ reporter
125. Severe metabolic acidosis causes early lethality in NBC1 W516X knock-in mice as a model of human isolated proximal renal tubular acidosis
126. Characterisation of factor IX with a glycine-to-valine missense mutation at residue 190 in a patient with severe haemophilia B
127. SEPT12 deficiency causes sperm nucleus damage and developmental arrest of preimplantation embryos
128. Reduced Paired Box 5 (PAX5) Expression Is Common In Childhood Pro-B Acute Lymphoblastic Leukemic Cells, However, Can Not Be Attributed to PAX5 Genetic Hemizygous Deletion Only
129. Multiplex Reverse Transcription-Polymerase Chain Reaction as Diagnostic Molecular Screening of 4 Common Fusion Chimeric Genes in Taiwanese Children With Acute Lymphoblastic Leukemia
130. Genetic Modification of Donor Hepatocytes Improves Therapeutic Efficacy for Hemophilia B in Mice
131. Roles of Thromboxane A2 On High Salt Induced-Fetal Defect.
132. The Expression Level of Septin12 Is Critical for Spermiogenesis
133. Pharmacogenomic variations in treatment protocols for childhood acute lymphoblastic leukemia
134. Down-Regulation of MicroRNA-143 and -145 in Childhood B-Lineage Acute Lymphoblastic Leukemia at Initial Diagnosis and in Relapse but up-Regulated When in Remission
135. The Importance of Pharmacogenomic Variations in the Treatment of Children with Acute Lymphoblastic Leukemia
136. MicroRNA Expression in Childhood Acute Lymphoblastic Leukemia (ALL)
137. Engineered Factor IX with Augmented Clotting Activities in a Hemophilia B Mouse Model.
138. L2dtl Is Essential for Cell Survival and Nuclear Division in Early Mouse Embryonic Development
139. Identification of Residues Asn89, Ile90, and Val107 of the Factor IXa Second Epidermal Growth Factor Domain That Are Essential for the Assembly of the Factor X-activating Complex on Activated Platelets
140. A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X–deficient family
141. SOCS1 methylation in patients with newly diagnosed acute myeloid leukemia
142. Identification of Functionally Important Residues of the Epidermal Growth Factor-2 Domain of Factor IX by Alanine-scanning Mutagenesis
143. The Distinct Roles That Gln-192 and Glu-217 of Factor IX Play in Selectivity for Macromolecular Substrates and Inhibitors
144. Domain Specific Monoclonal Anti-factor VIII Antibodies Generated by Inclusion Body-renatured Factor VIII Peptides
145. Mice Deficient in Hepsin, a Serine Protease, Exhibit Normal Embryogenesis and Unchanged Hepatocyte Regeneration Ability
146. Hemophilia B with Mutations at Glycine-48 of Factor IX Exhibited Delayed Activation by the Factor VIIa-tissue Factor Complex
147. A Nucleolus-Predominant piggyBac Transposase, NP-mPB, Mediates Elevated Transposition Efficiency in Mammalian Cells.
148. Functional Analysis of the Amino Terminus of Epstein-Barr Virus Deoxyribonuclease
149. Genetic alterations at the splice junction of p53 gene in human hepatocellular carcinoma
150. Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated SLC26A4 Gene in Humans and Mice.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.