SCOPUS 정보 검색 플랫폼

Epilepsia

Volumn 41, Issue 8, 2000, Pages 1070-1071

Molecular identity of the M-channel

(1) McKinnon, D a

a Stony Brook University (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DISEASE ASSOCIATION; ELECTROSTIMULATION; EPILEPSY; GENE EXPRESSION; GENE MUTATION; HUMAN; NERVE CELL EXCITABILITY; POTASSIUM CONDUCTANCE; PRIORITY JOURNAL;

EID: 0033883407 PISSN: 00139580 EISSN: None Source Type: Journal
DOI: 10.1111/j.1528-1157.2000.tb00303.x Document Type: Article

Times cited : (1)

References (10)

1
- 0008502578
- Currents
- Narahashi T, ed. Ion channels. New York: Plenum
- (1988) , pp. 55-94
- Brown, D.A.¹

2
- 0029068866
- Potassium channel expression in prevertebral and paravertebral sympathetic neurones: Control of firing properties
- (1998) J Physiol , vol.485 , pp. 319-335
- Wang, H.S.¹ McKinnon, D.²

3
- 0002635898
- Multiple channels and calcium dynamics
- Koch C, Segev I, eds. Methods in neuronal modeling. Cambridge, MA: Bradford
- (1989) , pp. 97-133
- Yamada, W.M.¹ Koch, C.² Adams, P.R.³

4
- 0018886033
- + current in a vertebrate neurone
- (1998) Nature , vol.283 , pp. 673-676
- Brown, D.A.¹ Adams, P.R.²

5
- 0019720867
- M-currents in voltage-clamped mammalian sympathetic neurones
- (1981) Neurosci Lett , vol.24 , pp. 289-294
- Constanti, A.¹ Brown, D.A.²

6
- 0032483972
- KCNQ2 and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel
- (1998) Science , vol.282 , pp. 1890-1893
- Wang, H.S.¹ Pan, Z.² Shi, W.³

7
- 0032536030
- A potassium channel mutation in neonatal epilepsy
- (1998) Science , vol.279 , pp. 403-406
- Biervert, C.¹ Schroeder, B.C.² Kubisch, C.³

8
- 0031974209
- A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
- (1998) Nat Genet , vol.18 , pp. 53-55
- Charlier, C.¹ Singh, N.A.² Ryan, S.G.³

9
- 17344372328
- A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
- (1998) Nat Genet , vol.18 , pp. 25-29
- Singh, N.A.¹ Charlier, C.² Stauffer, D.³

10
- 0028986844
- Benign familial neonatal convulsions: Confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q
- (1995) Hum Genet , vol.95 , pp. 411-415
- Steinlein, O.¹ Schuster, V.² Fischer, C.³ Haussler, M.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.