13 results on '"Hernan Imma"'
Search Results
2. Effect of the catechol‐O‐methyltransferase Val158Met polymorphism on theory of mind in obesity
3. Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene
4. The interaction effect between BDNF val66met polymorphism and obesity on executive functions and frontal structure
5. High-resolution melting analysis of the common c.1905+1G>A mutation causing dihydropyrimidine dehydrogenase deficiency and lethal 5-fluorouracil toxicity
6. Dopamine Genes (DRD2/ANKK1-TaqA1 and DRD4-7R) and Executive Function: Their Interaction with Obesity
7. Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing
8. Clinical pharmacogenomic testing of KRAS, BRAF and EGFRmutations by high resolution melting analysis and ultra-deep pyrosequencing
9. Cellular Expression and siRNA-Mediated Interference of Rhodopsincis-Acting Splicing Mutants Associated with Autosomal Dominant Retinitis Pigmentosa
10. Transcriptional expression ofcis-acting andtrans-acting splicing mutations cause autosomal dominant retinitis pigmentosa
11. Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population
12. Novelc-KIT germline mutation in a family with gastrointestinal stromal tumors and cutaneous hyperpigmentation
13. Mutations in the Pre-mRNA Splicing-Factor GenesPRPF3,PRPF8, andPRPF31in Spanish Families with Autosomal Dominant Retinitis Pigmentosa
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