163 results on '"Dai, Limeng"'
Search Results
2. Downregulation of miR-26b attenuates early brain injury induced by subarachnoid hemorrhage via mediating the KLF4/STAT3/HMGB1 axis
3. Imbalanced optimal feedback motor control system in spinocerebellar ataxia type 3.
4. Focusing Intracranial Aneurysm Lesion Segmentation by Graph Mask2Former with Local Refinement in DSA Images
5. LMNA-related muscular dystrophy involving myoblast proliferation and apoptosis through the FOXO1/GADD45A pathway
6. Deubiquitinating enzyme USP30 negatively regulates mitophagy and accelerates myocardial cell senescence through antagonism of Parkin
7. microRNA-130b May Induce Cerebral Vasospasm after Subarachnoid Hemorrhage via Modulating Kruppel-like Factor 4
8. Gray matter atrophy patterns within the cerebellum-neostriatum-cortical network in SCA3
9. A case report of NPHP1 deletion in Chinese twins with nephronophthisis
10. Supt16 Haploinsufficiency Impairs PI3K/AKT/mTOR/Autophagy Pathway in Human Pluripotent Stem Cells Derived Neural Stem Cells
11. A novel case of global developmental delay syndrome with microdeletion at 10p14–p15.3 and microduplication at 18p11.31–p11.32
12. Reduction of cerebral lactate level in 3-month-old APP/PS1 mouse: The relationship with Aβ production
13. Disruption of Intracellular Calcium Homeostasis Leads to ERLIN2-Linked Hereditary Spastic Paraplegia in Patient-Derived Stem Cell Models
14. Supt16 haploinsufficiency causes neurodevelopment disorder by disrupting MAPK pathway in neural stem cells
15. Overexpression of long non-coding RNA SOX2OT promotes esophageal squamous cell carcinoma growth
16. A Novel Splicing Mutation c.335-1 G gt; A in the Cardiac Transcription Factor NKX2-5 Leads to Familial Atrial Septal Defect Through miR-19 and PYK2
17. Early reduction of cerebral lactate in Alzheimer’s disease mouse model: The relationship with Aβ production
18. Network Reconfiguration Among Cerebellar Visual, and Motor Regions Affects Movement Function in Spinocerebellar Ataxia Type 3
19. Supt16 haploinsufficiency causes neurodevelopment disorder by disrupting MAPK pathway in neural stem cells.
20. Monocarboxylate Transporter 1 May Benefit Cerebral Ischemia via Facilitating Lactate Transport From Glial Cells to Neurons
21. X Chromosome Inactivation Pattern and Pregnancy Outcome of Female Carriers of Pathogenic Heterozygous X-Linked Deletions
22. Novel and Recurrent Mutations of STK11 Gene in Six Chinese Cases with Peutz–Jeghers Syndrome
23. Mutation p.Leu128Pro in the 1A domain of K16 causes pachyonychia congenita with focal palmoplantar keratoderma in a Chinese family
24. Confirmation of genetic homogeneity of syndactyly type IV and triphalangeal thumb–polysyndactyly syndrome in a Chinese family and review of the literature
25. A Tiered Genetic Screening Strategy for the Molecular Diagnosis of Intellectual Disability in Chinese Patients
26. Inhibition of Lactate-GPR81-PI3K/Akt Pathway May Exacerbate Aβ Aggregation in 3-Month-Old APP/PS1 Mice
27. Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics
28. Association between polymorphism in the promoter region of Interleukin 6 (-174 G/C) and risk of Alzheimer’s disease: a meta-analysis
29. Expression and Prognostic Role of PLOD1 in Malignant Glioma
30. Low Maternal Dietary Intake of Choline Regulates Toll‐Like Receptor 4 Expression Via Histone H3K27me3 in Fetal Mouse Neural Progenitor Cells
31. Expression and Prognostic Role of PLOD1 in Malignant Glioma
32. Potential biomarkers for inherited thrombocytopenia 2 identified by plasma proteomics.
33. Generation of the human induced pluripotent stem cell line (SHAMUi001-A) carrying the heterozygous c.-128G>T mutation in the 5′-UTR of the ANKRD26 gene
34. Nonsyndromic retinitis pigmentosa caused by two novel variants in the HGSNAT gene in a Chinese family
35. A Rare Big Chinese Family With Thrombocytopenia 2: A Case Report and Literature Review
36. E2F1 promotes cancer cell sensitivity to cisplatin by regulating the cellular DNA damage response through miR-26b in esophageal squamous cell carcinoma
37. PPARA genetic variants increase the risk for cardiac pumping function reductions following acute high‐altitude exposure: A self‐controlled study
38. Choline Supplementation Ameliorates Behavioral Deficits and Alzheimer's Disease‐Like Pathology in Transgenic APP/PS1 Mice
39. Homozygosity mapping and whole exome sequencing reveal a novel ERCC8 mutation in a Chinese consanguineous family with unique cerebellar ataxia
40. Genetic analysis in a cohort of patients with hereditary optic neuropathies in Southwest of China
41. Development of an Efficient Screening System for HDAC Inhibitor Based on TCF Response Element
42. A functional polymorphism rs2257440 in the gene DcR3 regulates its expression via MTF-1 in esophageal squamous cell carcinoma
43. Nonsmall cell lung cancer with rare exon 7 p.A289V mutation in the EGFR gene responds to Icotinib treatment
44. Low Maternal Dietary Intake of Choline Regulates Toll‐Like Receptor 4 Expression Via Histone H3K27me3 in Fetal Mouse Neural Progenitor Cells.
45. Trichostatin A induces p53‑dependent endoplasmic reticulum stress in human colon cancer cells
46. First report of a novel LMNA mutation in a Chinese family with limb-girdle muscular dystrophy
47. Trichostatin A induces p53-dependent endoplasmic reticulum stress in human colon cancer cells.
48. Development of an Efficient Screening System for HDAC Inhibitor Based on TCF Response Element
49. miR-203 Is a Direct Transcriptional Target of E2F1 and Causes G1 Arrest in Esophageal Cancer Cells
50. GW25-e5357 Influence of angiotensin-converting enzyme gene insertion/deletion polymorphism on occurrence and recurrence of atrial fibrillation: A systematic review and Meta-analysis
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