Suchergebnisse - "KUNKEL LOUIS M"

PubPharm (312)

61

Fam65b is important for formation of the HDAC6-dysferlin protein complex during myogenic cell differentiation

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2014

von Balasubramanian, A. | Kawahara, G. | Gupta, V. | +4

62

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G)

enthalten in: Human molecular genetics | 2014

von Vieira, N. | Naslavsky, M. | Licinio, L. | +16

63

MicroRNA-486-dependent modulation of DOCK3/PTEN/AKT signaling pathways improves muscular dystrophy-associated symptoms

enthalten in: The Journal of clinical investigation | 2014

von Alexander, M. | Casar, J. | Motohashi, N. | +13

64

Human skeletal muscle xenograft as a new preclinical model for muscle disorders

enthalten in: Human molecular genetics | 2014

von Zhang, Y. | King, O. | Rahimov, F. | +8

65

Dystrophin is a tumor suppressor in human cancers with myogenic programs

enthalten in: Nature genetics | 2014

von Wang, Y. | Marino-Enriquez, A. | Bennett, R. | +17

66

Dystrophin is a tumor suppressor in human cancers with myogenic programs

enthalten in: Nature genetics | 2014

von Wang, Y. | Marino-Enriquez, A. | Bennett, R. | +17

CommentIn: Cell Cycle. 2015;14(17):2713-4. - PMID 26101897

67

Human skeletal muscle xenograft as a new preclinical model for muscle disorders

enthalten in: Human molecular genetics | 2014

von Zhang, Y. | King, O. | Rahimov, F. | +8

68

Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling

enthalten in: Human molecular genetics | 2014

von Kawahara, G. | Gasperini, M. | Myers, J. | +7

ErratumIn: Hum Mol Genet. 2015 Aug 1;24(15):4480-1. - PMID 26034133

69

Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling

enthalten in: Human molecular genetics | 2014

von Kawahara, G. | Gasperini, M. | Myers, J. | +7

70

Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis

enthalten in: Molecular autism | 2014

von Kong, S. | Sahin, M. | Collins, C. | +7