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253 results on '"Gharavi A"'

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1. Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence

2. Mapping the human genetic architecture of COVID-19

3. Detection of viral gene expression in risk‐stratified biopsies reveals no active HPV in cutaneous squamous cell carcinoma

4. De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis

5. Considerable increase in Poly(3-hydroxybutyrate) production via phbC gene overexpression in Ralstonia eutropha PTCC 1615

6. A survey of intact low-density polyethylene film biodegradation by terrestrial Actinobacterial species

7. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

8. Leukemia Inhibitory Factor Signaling Enhances Production of Galactose-Deficient IgA1 in IgA Nephropathy

9. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits

10. GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy

11. Simultaneous disruption of circulating miR‐21 and cytotoxic T lymphocytes (CTLs): Prospective diagnostic and prognostic markers foresophageal squamous cell carcinoma(ESCC)

12. Whole-genome sequencing of patients with rare diseases in a national health system

13. Medical Records-Based Genetic Studies of the Complement System

14. Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19

15. Assessment of vital organ histopathology and plasma oxidative conditions of rainbow trout Oncorhynchus mykiss reared in earthen saltwater pond

16. Ecological role of Acinetobacter calcoaceticus GSN3 in natural biofilm formation and its advantages in bioremediation

17. Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

18. A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes

19. Comprehensive study of antimicrobial susceptibility pattern and extended spectrum beta-lactamase (ESBL) prevalence in bacteria isolated from urine samples

20. Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

21. Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

23. Characterization of a multi-epitope peptide with selective MHC-binding capabilities encapsulated in PLGA nanoparticles as a novel vaccine candidate against Toxoplasma gondii infection

24. Effects of dietary phytol supplementation on growth performance, immunological parameters, antioxidant and stress responses to ammonia exposure in common carp, Cyprinus carpio (Linnaeus, 1758)

25. Inhibition of STAT3 Signaling Reduces IgA1 Autoantigen Production in IgA Nephropathy

26. A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling

27. Cases in Precision Medicine: APOL1 and Genetic Testing in the Evaluation of Chronic Kidney Disease and Potential Transplant

28. Evaluation of Three Different Laboratory Methods for Identifi-cation of Pneumocystis jirovecii Pneumonia (PCP) among HIV Positive Asymptomatic Prisoners

29. Toxocara Infection in Asthmatic Children: A Case-Control Study in Karaj District, Iran

30. The copy number variation landscape of congenital anomalies of the kidney and urinary tract

31. Genome‐wide association study in mice identifies loci affecting liver‐related phenotypes including Sel1l influencing serum bile acids

32. Somatic Mutations Modulate Autoantibodies against Galactose-Deficient IgA1 in IgA Nephropathy

33. Degenerate primers as biomarker for gene-targeted metagenomics of the catechol 1, 2-dioxygenase-encoding gene in microbial populations of petroleum-contaminated environments

34. Genetic studies of body mass index yield new insights for obesity biology

35. Trans-ethnic genome-wide association study of kidney function provides novel insight into effector genes and causal effects on kidney-specific disease aetiologies

36. Exome-Based Rare-Variant Analyses in CKD

37. Molecular Discrimination of the Candida parapsilosis Species Complex via SADH Gene Analysis and Evaluation of Proteinase Activity Among the Isolates

38. Highly efficient phenol degradation in a batch moving bed biofilm reactor: benefiting from biofilm-enhancing bacteria

39. Deep Phenotyping on Electronic Health Records Facilitates Genetic Diagnosis by Clinical Exomes

40. Determination of novel members in the Drosophila melanogaster anteriorposterior patterning system using natural variation

41. Genomics and Drug Transporters and Application in Drug Discovery, Delivery, and Development

42. Frequency of Anti-Toxoplasma IgM and IgG Antibodies in Leukemic Patients

43. Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

44. The mitochondrial uncoupler DNP triggers brain cell mTOR signaling network reprogramming and CREB pathway up-regulation

45. Biochemical and physiological responses of Brassica napus plants to humic acid under water stress

46. Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

47. Prevalence of Anti-Toxoplasma gondii Antibodies in Young Iranians: The CASPIAN III Study

48. The role of probiotic Lactobacillus acidophilus ATCC 4356 bacteriocin on effect of HBsu on planktonic cells and biofilm formation of Bacillus subtilis

49. GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

50. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

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