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256 results on '"Grinberg, D"'

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1. La variante missense rs2908004 de WNT16 actúa como eQTL de FAM3C en osteoblastos primarios humanos

3. Búsqueda de variantes del gen LRP4 en mujeres con alta masa ósea y en pacientes con malformación de Chiari tipo I

4. Estudios funcionales de variantes de DKK1 presentes en la población general

5. Estudio genético de la fractura femoral atípica mediante la secuenciación del exoma en tres hermanas afectas y tres pacientes no relacionadas

6. Identificación de variantes genéticas asociadas con la densidad mineral ósea (DMO) en el gen FLJ42280

7. Estudio del patrón de expresión de microRNAs en el hueso osteoporótico

8. Decidable characterizations of dynamical properties for additive cellular automata over a finite abelian group with applications to data encryption

9. An efficiently computable characterization of stability and instability for linear cellular automata

10. SNPs en el 3’UTR de gen RANK determinan la fractura osteoporótica sitio-dependiente

11. Dynamical behavior of additive cellular automata over finite abelian groups

12. Chaos and ergodicity are decidable for linear cellular automata over (Z/mZ)n

13. From linear to additive cellular automata

14. Transcatheter edge-to-edge mitral valve repair following surgical annuloplasty with ring implantation. Results from the multicenter “Clip-in-Ring” registry

16. Spontaneous idiopathic aneurysm of the inferior vena cava

17. Additive Cellular Automata Over Finite Abelian Groups: Topological and Measure Theoretic Properties

28. Genetic study of atypical femoral fractures using exome sequencing in three affected sisters and three unrelated patients

29. Functional studies of DKK1 variants present in the general population

32. Functional Characterization of a GGPPS Variant Identified in Atypical Femoral Fracture Patients and Delineation of the Role of GGPPS in Bone-Relevant Cell Types

33. Identificación de variantes genéticas asociadas con la densidad mineral ósea (DMO) en el gen FLJ42280

35. The spectrum of niemann-pick type C disease in greece

37. The association between common vitamin D receptor gene variations and osteoporosis

38. Identificación de variantes genéticas asociadas con la densidad mineral ósea (DMO) en el gen FLJ42280

39. Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: Clinical and molecular findings in 11 patients

40. MiRNA profiling of whole trabecular bone: identification of osteoporosis-related changes in MiRNAs in human hip bones

41. Estudio del patrón de expresión de microRNAs en el hueso osteoporótico

42. Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes

43. Niemann-Pick type C disease: A novel NPC1 mutation segregating in a Greek island

44. Cholesterol Regulates Syntaxin 6 Trafficking at trans-Golgi Network Endosomal Boundaries

45. Genetic analysis of high bone mass cases from the BARCOS cohort of Spanish postmenopausal women

46. SNPs en el 3'UTR de gen RANK determinan la fractura osteoporótica sitio-dependiente

47. Estudio clínico y molecular en una familia con osteocondromatosis múltiple.

49. Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: Clinical, genetic, and functional studies

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