510 results on '"Takada, Shuji"'
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2. Turnover of mammal sex chromosomes in the Sry -deficient Amami spiny rat is due to male-specific upregulation of Sox9
3. A novel mucopolysaccharidosis type II mouse model with an iduronate-2-sulfatase-P88L mutation
4. Conservation and divergence of canonical and non-canonical imprinting in murids
5. Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome
6. Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II
7. STAT6 gain-of-function variant exacerbates multiple allergic symptoms
8. LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion
9. Sexual fate of murine external genitalia development : Conserved transcriptional competency for male-biased genes in both sexes
10. GATA4 binding to the Sox9 enhancer mXYSRa/Enh13 is critical for testis differentiation in mouse.
11. Tmsb10 triggers fetal Leydig differentiation by suppressing the RAS/ERK pathway
12. Corrigendum to “Enhanced osteoblastic differentiation of parietal bone in a novel murine model of mucopolysaccharidosis type II” [Molecular Genetics and Metabolism Reports Vol. 37, December 2023, 101021]
13. ZNF445: a homozygous truncating variant in a patient with Temple syndrome and multilocus imprinting disturbance
14. LMNAQ353R Mutation Causes Dilated Cardiomyopathy Through Impaired Vitamin D Signaling
15. Estimation of Higher-Order State Variables by Polynomial Approximation Considering Quantization Step Size of Encoder and the Implementation on FPGA
16. Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice
17. Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2)
18. RNA-Based Therapeutic Technology
19. SAT264 Effects Of Coenzymes In Gene Therapy For Congenital Adrenal Hyperplasia With AAV Vectors Into Model Mice
20. Fetal Therapy Model of Myelomeningocele with Three-Dimensional Skin Using Amniotic Fluid Cell-Derived Induced Pluripotent Stem Cells
21. CRISPR/Cas9-mediated simultaneous knockout of Dmrt1 and Dmrt3 does not recapitulate the 46,XY gonadal dysgenesis observed in 9p24.3 deletion patients
22. In vivo maturation of human embryonic stem cell-derived teratoma over time
23. Conditional deletion of CD98hc inhibits osteoclast development
24. Efficient production and transmission of CRISPR/Cas9-mediated mutant alleles at the IG-DMR via generation of mosaic mice using a modified 2CC method
25. Usp26 mutation in mice leads to defective spermatogenesis depending on genetic background
26. Comparative analysis demonstrates cell type-specific conservation of SOX9 targets between mouse and chicken
27. Publisher Correction: Calaxin is required for cilia-driven determination of vertebrate laterality
28. Calaxin is required for cilia-driven determination of vertebrate laterality
29. Temple syndrome in a patient with variably methylated CpGs at the primary MEG3/DLK1:IG-DMR and severely hypomethylated CpGs at the secondary MEG3:TSS-DMR
30. Modeling of Retina and Optic Nerve Ischemia–Reperfusion Injury through Hypoxia–Reoxygenation in Human Induced Pluripotent Stem Cell-Derived Retinal Ganglion Cells.
31. Chromosomal microdeletion leading to pituitary gigantism through hormone-gene overexpression
32. TEAD1 trapping by the Q353R–Lamin A/C causes dilated cardiomyopathy
33. Supplementary Figures S1-S2 from Multiplex Reverse Transcription-PCR Screening for EML4-ALK Fusion Transcripts
34. Supplementary Data from KIF5B-ALK, a Novel Fusion Oncokinase Identified by an Immunohistochemistry-based Diagnostic System for ALK-positive Lung Cancer
35. Supplementary Figure 2 from Identification of Novel Isoforms of the EML4-ALK Transforming Gene in Non–Small Cell Lung Cancer
36. Supplementary Figure 1 from Identification of Novel Isoforms of the EML4-ALK Transforming Gene in Non–Small Cell Lung Cancer
37. Genome editing for the reproduction and remedy of human diseases in mice
38. Dissecting the roles of miR-140 and its host gene
39. Integrator complex subunit 15 controls mRNA splicing and is critical for eye development
40. DNA methylation signature inNSD2loss-of-function variants appeared similar to that in Wolf-Hirschhorn syndrome
41. 網羅的ゲノム解析を端緒に新規の分子病態の解明に至った重症アトピー性皮膚炎、喘息、食物アレルギー、好酸球性胃腸炎等を呈する疾患と標的治療薬開発の可能性
42. Establishment and visual analysis of CBA/J-Pde6bY347Y/Y347X and C3H/HeJ-Pde6bY347Y/Y347X mice
43. Lysosomal Acid Lipase Deficiency: Genetics, Screening, and Preclinical Study
44. The Mohawk homeobox transcription factor regulates the differentiation of tendons and volar plates
45. Mapping of a responsible region for sex reversal upstream of Sox9 by production of mice with serial deletion in a genomic locus
46. Peptidyl arginine deiminase 2 (Padi2) is expressed in Sertoli cells in a specific manner and regulated by SOX9 during testicular development
47. POU1F1/Pou1f1 c.143-83A > G Variant Disrupts the Branch Site in Pre-mRNA and Leads to Dwarfism
48. LBODP008 Gene Therapy For Congenital Adrenal Hyperplasia With AAV Vectors Into Fibroblasts, IPS Cells And Model Mice
49. Lipid Nanoparticles: A Novel Gene Delivery Technique for Clinical Application
50. L-Sox5 and Sox6 Proteins Enhance Chondrogenic miR-140 MicroRNA Expression by Strengthening Dimeric Sox9 Activity
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