50 results on '"Meguro‐Horike, Makiko"'
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2. The matricellular protein Fibulin-5 regulates β-cell proliferation in an autocrine/paracrine manner
3. Super-enhancer trapping by the nuclear pore via intrinsically disordered regions of proteins in squamous cell carcinoma cells
4. Overlapping role of c-Jun N-terminal kinase (JNK) 1 and 2 in imidazole ketone erastin-induced ferroptosis
5. Renal Pharmacokinetic Adaptation to Cholestasis Causes Increased Nephrotoxic Drug Accumulation by Mrp6 Downregulation in Mice
6. Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency
7. Functional analysis of two abnormal antithrombin proteins with different intracellular kinetics
8. Targeting cis-regulatory elements of FOXO family is a novel therapeutic strategy for induction of leukemia cell differentiation
9. A maternal high-fat diet induces fetal origins of NASH-HCC in mice
10. ROCK‐dependent phosphorylation of NUP62 regulates p63 nuclear transport and squamous cell carcinoma proliferation
11. UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons
12. Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes
13. Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles
14. Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate
15. Cancer stem-like properties and gefitinib resistance are dependent on purine synthetic metabolism mediated by the mitochondrial enzyme MTHFD2
16. Protein S deficiency caused by cryptic splicing due to the novel intron variant c.346+5G>C in PROS1
17. Parental deprivation in early childhood impacts gene expression on brain development as a lifelong effect
18. Potential therapeutic target secretogranin II might cooperate with hypoxia‐inducible factor 1α in sunitinib‐resistant renal cell carcinoma
19. Nuclear transport surveillance of p53 by nuclear pores in glioblastoma
20. Pancreatic solitary fibrous tumor causing ectopic adrenocorticotropic hormone syndrome
21. ASH2L, a COMPASS core subunit, is involved in the cell invasion and migration of triple-negative breast cancer cells through the epigenetic control of histone H3 lysine 4 methylation
22. Epigenetic alterations of 11beta-hydroxysteroid dehydrogenase 1 gene in the adipose tissue of patients with primary aldosteronism
23. Functional Analysis of Two Abnormal Antithrombin Proteins with Different Intracellular Kinetics
24. Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency
25. Topical estrogen application promotes cutaneous wound healing in db/db female mice with type 2 diabetes
26. MMCT-Mediated Chromosome Engineering Technique Applicable to Functional Analysis of lncRNA and Nuclear Dynamics
27. First report of inherited protein S deficiency caused by paternal PROS1 mosaicism
28. Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC
29. MUSASHI‐2 confers resistance to third‐generation EGFR‐tyrosine kinase inhibitor osimertinib in lung adenocarcinoma
30. Effect of potassium on DNA methylation of aldosterone synthase gene
31. Epigenetic Defects Related Reproductive Technologies: Large Offspring Syndrome (LOS)
32. 15q11.2–13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain
33. Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome
34. Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate
35. Aging-associated impairment in metabolic compensation by subcutaneous adipose tissue promotes diet-induced fatty liver disease in mice
36. Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophy
37. Cancer stem-like properties and gefitinib resistance are dependent on purine synthetic metabolism mediated by the mitochondrial enzyme MTHFD2
38. Epigenetic Regulation of Aldosterone Synthase Gene by Sodium and Angiotensin II
39. Bromodomain protein BRD4 inhibitor JQ1 regulates potential prognostic molecules in advanced renal cell carcinoma
40. Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation.
41. Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation
42. MMCT-Mediated Chromosome Engineering Technique Applicable to Functional Analysis of lncRNA and Nuclear Dynamics.
43. Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell–Silver syndrome
44. Aire controls the differentiation program of thymic epithelial cells in the medulla for the establishment of self-tolerance
45. Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution
46. Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution
47. Epigenetic alterations of 11beta-hydroxysteroid dehydrogenase 1 gene in the adipose tissue of patients with primary aldosteronism.
48. First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.
49. MMCT-mediated chromosome engineering technique applicable to functional analysis of lncRNA and nuclear dynamics.
50. Aire controls the differentiation program of thymic epithelial cells in the medulla for the establishment of self-tolerance.
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