39 results on '"Molano, Jesús"'
Search Results
2. Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis
3. Regulation of connexin hemichannel activity by membrane potential and the extracellular calcium in health and disease
4. Screening for mutations in Spanish families with myotonia. Functional analysis of novel mutations in CLCN1 gene
5. Distribution of Chitin in the Yeast Cell Wall: An Ultrastructural and Chemical Study
6. Molecular diagnosis of limb-girdle muscular dystrophy type 2A by next-generation sequencing
7. Recomendaciones para la elaboración de informes genéticos de diagnóstico en el ámbito asistencial
8. Genetic basis of end-stage hypertrophic cardiomyopathy
9. A novel PLP1 deletion causing classic Pelizaeus-Merzbacher disease
10. The G397A (E133K) change in the AGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population
11. Recomendaciones para la elaboración de informes genéticos de diagnóstico en el ámbito asistencial
12. El final de una época
13. Directional coupling of oligodendrocyte connexin‐47 and astrocyte connexin‐43 gap junctions
14. Functional Domain Analysis of the Yeast ABC Transporter Ycf1p by Site-directed Mutagenesis
15. Diagnóstico prenatal y diagnóstico preconcepcional. Perspectivas del análisis genético
16. CF2603/4delT, a new frameshift mutation in exon 13 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene
17. Molecular diagnosis of limb-girdle muscular dystrophy type 2A by next-generation sequencing
18. Recommendations of good practices for the genetic diagnosis of myotonic dystrophy
19. Recomendaciones de buenas prácticas para el diagnóstico genético de la distrofia miotónica
20. Sobre el fraude científico
21. Screening of Specific Gene Mutations Associated with Cystic Fibrosis
22. Yo soy yo y mi microbiota (parafraseando a Ortega y Gasset)
23. Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes
24. High-Risk Hypertrophic Cardiomyopathy Associated With a Novel Mutation in Cardiac Myosin-Binding Protein C
25. Miocardiopatía hipertrófica de alto riesgo asociada con una nueva mutación en la proteína C fijadora de miosina
26. The G397A (E133K) change in theAGGF1 (VG5Q) gene is a single nucleotide polymorphism in the Spanish population
27. A novel insertion in theFGFR2gene in a patient with Crouzon phenotype and sacrococcygeal tail
28. Miocardiopatía hipertrófica: Baja frecuencia de mutaciones en el gen de la cadena pesada de la betamiosina cardiaca
29. Domain Interactions in the Yeast ATP Binding Cassette Transporter Ycf1p: Intragenic Suppressor Analysis of Mutations in the Nucleotide Binding Domains
30. Distrofia miotónica: inestabilidad del ADN en gemelas monocigóticas
31. Screening for cystic fibrosis mutations in Spanish patients
32. Interplay between DMD Point Mutations and Splicing Signals in Dystrophinopathy Phenotypes.
33. ¿Existen determinantes genéticos para un envejecimiento sano?
34. Antibodies to vimentin intermediate filaments in sera from patients with systemic lupus erythematosus.
35. A novel insertion in the FGFR2 gene in a patient with Crouzon phenotype and sacrococcygeal tailPresented at the 11th Annual Meeting of the Spanish Society of Clinical Genetics and Dysmorphology, Murcia, Spain, March 2002.
36. A rapid and sensitive assay for chitinase using tritiated chitin
37. Purification and properties of a d-fructose 1,6-bisphosphatase from Saccharomyces cerevisiae
38. Electroretinogram in Duchenne/Becker Muscular Dystrophy
39. [Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.