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1. Implementation of diabetes care and educational program via telemedicine in patients with COVID‐19 in home isolation in Thailand: A real‐worldexperience

2. Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome

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3. Independent associations of urine neutrophil gelatinase–associated lipocalin and serum uric acid with interstitial fibrosis and tubular atrophy in primary glomerulonephritis

4. Effects of Therapy on Urine Neutrophil Gelatinase-Associated Lipocalin in Nondiabetic Glomerular Diseases with Proteinuria

5. Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation.

6. Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand

14. Mitochondrial DNA sequence analysis in congenital myotonic dystrophy

15. Cellular responses of histatin-derived peptides immobilized titanium surface using a tresyl chloride-activated method.

16. Development of silicon nitride ceramic for CAD/CAM restoration.

17. Trephination-based, guided surgical implant placement: A clinical study.

18. Thyroid function is associated with body mass index and fasting plasma glucose in Thai euthyroid population.

19. Comparison of excursive occlusal force parameters in post-orthodontic and non-orthodontic subjects using T-Scan® III.

24. A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I

25. A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome

26. Physicochemical Properties and Biological Response of Titanium Surface Modified by Anodic Spark Deposition for Dental Implants.

27. Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai population.

29. Mitochondrial DNA Haplogroup Distribution in Pedigrees of Southeast Asian G11778A Leber Hereditary Optic Neuropathy.

31. Novel Silicon Based Anodic Spark Deposition Treatment for Dental Implant

33. Mitochondrial DNA polymorphism in substantia nigra

34. Proportion of 11778 Mutant Mitochondrial DNA and Clinical Expression in a Thai Population With Leber Hereditary Optic Neuropathy

35. Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber's hereditary optic neuropathy: A case report.

36. Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome.

37. The prehistoric peopling of Southeast Asia.

38. Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.

39. Exome sequencing in Thai patients with familial obesity.

40. A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.

41. Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation.

42. Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.

43. Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations.

44. Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand.

45. Polyglutamined expanded androgen receptor interacts with chaperonin CCT.

46. Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye.

47. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.

48. Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis.

49. Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation.

50. Oculopharyngodistal myopathy in a Thai family.