198 results on '"Fardaei, Majid"'
Search Results
2. High dietary inflammatory index (DII) scores increase odds of overweight in adults with rs9939609 polymorphism of FTO gene
3. The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients
4. Clinical and genetic-epigenetic aspects of recurrent hydatidiform mole: A review of literature
5. The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults
6. Studies on the molecular mechanism underlying myotonic dystrophy
7. An immunocompetent patient with a nonsense mutation in NHEJ1 gene
8. The effect of methyl donor supplementation on body composition, homocysteine, lipid profile and appetite regulatory hormones in overweight and obese adults: a randomized placebo-controlled trial
9. Inferior Spear-like Lens Opacity as a Sign of Keratoconus
10. Segmental Duplications as a Complement Strategy to Short Tandem Repeats in the Prenatal Diagnosis of Down Syndrome
11. Featured Cover
12. Expression of α2, α5 and α6 subunits of integrin in de-differentiated NIH3T3 cells by cell-free extract of embryonic stem cells
13. Novel pathogenic variants inNLRP7,NLRP5 ,andPADI6in patients with recurrent hydatidiform moles and reproductive failure
14. Auricular or body acupuncture: which one is more effective in reducing abdominal fat mass in Iranian men with obesity: a randomized clinical trial
15. The novel mutation in the COL7A1 gene in the patient with dystrophic forms of epidermolysis bullosa
16. Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa.
17. Effects of auricular acupressure combined with low-calorie diet on the leptin hormone in obese and overweight Iranian individuals
18. Recurrent pregnancy loss in the female with a heterozygous mutation in KHDC3L gene
19. The FOXG1-related syndrome with two novel mutations in the FOXG1 gene
20. CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 gene
21. Randomized Controlled Trial Effect of Short-Term MIND Diet Intervention on Hunger Hormones, Anthropometric Parameters, and Brain Structures in Middle-Aged Obese Women
22. Two novel mutations in the MECP2 gene in patients with Rett syndrome
23. Genetic analysis of Usher syndrome associated genes in Iranian pedigrees: The prominent role of MYO7A gene
24. Commentary: Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing
25. Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults
26. Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells
27. In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts
28. Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure.
29. Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient
30. Development of biliary and renal stone and sludge after taking Ceftriaxone is associated with a defect in UDP‐Glucuronosyltransferase (ie Gilbert’s syndrome)
31. Novel mutation in the MED23 gene for intellectual disability: A case report and literature review
32. Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran
33. The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions
34. Report of three cases with hereditary spastic paraplegia and investigation of the mutations
35. Identification of mutations in HEXA and HEXB in Sandhoff and Tay-Sachs diseases: a new large deletion caused by Alu elements in HEXA
36. Neurodegeneration with brain iron accumulation 2A: Report of four independent cases
37. Author's reply
38. TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis
39. Identification of a novel deletion withinALDH3A2 gene in an Iranian Familywith Sjögren-Larsson Syndrome
40. Mutation analysis of the CTNS gene in Iranian patients with infantile nephropathic cystinosis: identification of two novel mutations
41. Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene
42. Erratum: The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions
43. A New Mutation in WT1 Gene Associated with Wilms Tumor with Reduced Penetrance in an Iranian Family
44. Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports
45. A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
46. Prevalence of 2 UGT1A1 Gene Variations Related to Gilbert’s Syndrome in South of Iran: An Epidemiological, Clinical, and Genetic Study
47. Investigation of Common Variations of ABCB4, ATP8B1 and ABCB11 Genes in Patients with Progressive Familial Intrahepatic Cholestasis
48. Does the c.-273T>C variant in the upstream region of the HBB gene cause a thalassemia phenotype?
49. Association of FTOrs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults
50. A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure.
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