98 related articles for article (PubMed ID: 2197156)
1. Muscular dysgenesis: a model system for studying skeletal muscle development.
Powell JA
FASEB J; 1990 Jul; 4(10):2798-808. PubMed ID: 2197156
[TBL] [Abstract][Full Text] [Related]
2. Muscular dysgenesis in mice: a model system for studying excitation-contraction coupling.
Adams BA; Beam KG
FASEB J; 1990 Jul; 4(10):2809-16. PubMed ID: 2165014
[TBL] [Abstract][Full Text] [Related]
3. Restoration of dysgenic muscle contraction and calcium channel function by co-culture with normal spinal cord neurons.
Rieger F; Bournaud R; Shimahara T; Garcia L; Pinçon-Raymond M; Romey G; Lazdunski M
Nature; 1987 Dec 10-16; 330(6148):563-6. PubMed ID: 2446145
[TBL] [Abstract][Full Text] [Related]
4. Early effects in vitro of the muscular dysgenesis mutation on nervous tissue in the mouse.
Wieczorek DF
Muscle Nerve; 1984; 7(3):179-93. PubMed ID: 6708964
[TBL] [Abstract][Full Text] [Related]
5. Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis.
Knudson CM; Chaudhari N; Sharp AH; Powell JA; Beam KG; Campbell KP
J Biol Chem; 1989 Jan; 264(3):1345-8. PubMed ID: 2536362
[TBL] [Abstract][Full Text] [Related]
6. Rescue of excitation-contraction coupling in dysgenic muscle by addition of fibroblasts in vitro.
Courbin P; Koenig J; Ressouches A; Beam KG; Powell JA
Neuron; 1989 Apr; 2(4):1341-50. PubMed ID: 2560638
[TBL] [Abstract][Full Text] [Related]
7. Restoration of normal function in genetically defective myotubes by spontaneous fusion with fibroblasts.
Chaudhari N; Delay R; Beam KG
Nature; 1989 Oct; 341(6241):445-7. PubMed ID: 2507925
[TBL] [Abstract][Full Text] [Related]
8. Myotube driven myogenic recruitment of cells during in vitro myogenesis.
Breton M; Li ZL; Paulin D; Harris JA; Rieger F; Pinçon-Raymond M; Garcia L
Dev Dyn; 1995 Feb; 202(2):126-36. PubMed ID: 7734731
[TBL] [Abstract][Full Text] [Related]
9. A single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mdg) mice.
Chaudhari N
J Biol Chem; 1992 Dec; 267(36):25636-9. PubMed ID: 1281468
[TBL] [Abstract][Full Text] [Related]
10. Restoration of normal ultrastructure after expression of the alpha 1 subunit of the L-type Ca2+ channel in dysgenic myotubes.
Seigneurin-Venin S; Song M; Pinçon-Raymond M; Rieger F; Garcia L
FEBS Lett; 1994 Apr; 342(2):129-34. PubMed ID: 8143864
[TBL] [Abstract][Full Text] [Related]
11. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs.
Adams BA; Tanabe T; Mikami A; Numa S; Beam KG
Nature; 1990 Aug; 346(6284):569-72. PubMed ID: 2165571
[TBL] [Abstract][Full Text] [Related]
12. Appearance of the slow Ca conductance in myotubes from mutant mice with "muscular dysgenesis".
Bournaud R; Shimahara T; Garcia L; Rieger F
Pflugers Arch; 1989 Aug; 414(4):410-5. PubMed ID: 2477792
[TBL] [Abstract][Full Text] [Related]
13. Formation of triads without the dihydropyridine receptor alpha subunits in cell lines from dysgenic skeletal muscle.
Powell JA; Petherbridge L; Flucher BE
J Cell Biol; 1996 Jul; 134(2):375-87. PubMed ID: 8707823
[TBL] [Abstract][Full Text] [Related]
14. Ca2+ entry through acetylcholine receptor channel in dysgenic myotubes.
Melliti K; Bournaud R; Shimahara T
Arch Physiol Biochem; 1996; 104(1):57-61. PubMed ID: 8724881
[TBL] [Abstract][Full Text] [Related]
15. Restoration of dysgenic murine (mdg) myotube contraction after addition of Schwann cells from normal mice in vitro.
Courbin P; Do Thi A; Ressouches A; Dussartre C; Powell JA; Koenig J
Biol Cell; 1989; 67(3):355-8. PubMed ID: 2620167
[TBL] [Abstract][Full Text] [Related]
16. [Effect of the mutation muscular dysgenesis on the mitochondrial metabolism of fibroblasts in vitro].
Aymard C; Malgat M; Mazat JP; Koenig J
C R Acad Sci III; 1993; 316(5):529-32. PubMed ID: 8221238
[TBL] [Abstract][Full Text] [Related]
17. Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA.
Tanabe T; Beam KG; Powell JA; Numa S
Nature; 1988 Nov; 336(6195):134-9. PubMed ID: 2903448
[TBL] [Abstract][Full Text] [Related]
18. The muscular dysgenesis mutation in mice leads to arrest of the genetic program for muscle differentiation.
Chaudhari N; Beam KG
Dev Biol; 1989 Jun; 133(2):456-67. PubMed ID: 2731637
[TBL] [Abstract][Full Text] [Related]
19. Contractions of dysgenic skeletal muscle triggered by a potentiated, endogenous calcium current.
Adams BA; Beam KG
J Gen Physiol; 1991 Apr; 97(4):687-96. PubMed ID: 1711572
[TBL] [Abstract][Full Text] [Related]
20. Receptor-triggered polyphosphoinositide turnover produces less cytosolic free calcium in cultured dysgenic myotubes than in normal myotubes.
Tassin AM; Häggblad J; Heilbronn E
Muscle Nerve; 1990 Feb; 13(2):142-5. PubMed ID: 2314417
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
