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1. Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis

4. NAD+ depletion enhances reovirus-induced oncolysis in multiple myeloma

8. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

10. Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis

11. Neglected SARS-CoV-2 variants and potential concerns for molecular diagnostics: a framework for nucleic acid amplification test target site quality assurance

16. The DataHarmonizer: a tool for faster data harmonization, validation, aggregation and analysis of pathogen genomics contextual information

20. The Dataharmonizer: a Tool for Faster Data Harmonization, Validation, Aggregation, and Analysis of Pathogen Genomics Contextual Information

21. Soporte familiar y habilidades cognitivas en tiempos de pandemia de los estudiantes del distrito de Parcona, 2021

24. DMG26

29. List of Contributors

31. Association of Rare CYP39A1 Variants with Exfoliation Syndrome Involving the Anterior Chamber of the Eye

32. Phenotypic Overlap Between Familial Exudative Vitreoretinopathy and Microcephaly, Lymphedema, and Chorioretinal Dysplasia Caused by KIF11 Mutations

34. Complete response of a colonic high-grade neuroendocrine carcinoma to platinum-based therapy: Insights from comprehensive genomic profiling.

35. Diagnosis of adult glioma: A comparison of a custom NGS AmpliSeq panel to WHO 2016 glioma classification practice guidelines.

40. Low‐depth sequencing for copy number abnormalities in multiple myeloma supersedes fluorescent in situ hybridization in scope and resolution

41. GENETIC DETERMINANTS OF WEIGHT CHANGE DURING ANTIDEPRESSANT TREATMENT WITH SELECTIVE SEROTONIN RE-UPTAKE INHIBITORS: GENOME-WIDE STUDY AND META-ANALYSIS

42. Doses of Nearby Nature Simultaneously Associated with Multiple Health Benefits

43. KSHV lytic mRNA is efficiently translated in the absence of eIF4F

47. Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia

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