Article: A functional null mutation of SCN1B in a patient with Dravet syndrome.
Full Text (publisher's website) ; Article Metadata ; Article Data (extracted) Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL J. Neurosci., 2009
Inferred neuron-electrophysiology data values
Metadata values
| Experimental condition | Value |
|---|---|
| RecTemp | 30.0 |
| AnimalAge | 17.0 - 19.0 |
| Strain | C57BL |
| PrepType | in vitro |
| ElectrodeType | Patch-clamp |
| Species | Mice |
| ExternalSolution | 5.0 |
| external_1_Mg | 2.5 |
| external_1_Ca | 1.3 |
| external_1_Na | 146.0 |
| external_1_Cl | 129.1 |
| external_1_K | 2.5 |
| InternalSolution | 5.0 |
| internal_1_pH | 7.3 |
| internal_1_Mg | 2.0 |
| internal_1_Ca | 1.0 |
| internal_1_Na | 5.0 |
| internal_1_Cl | 7.0 |
| JxnPotential | Unreported |
| internal_0_pH | 7.26 |
| internal_0_Mg | 2.0 |
| internal_0_Na | 17.0 |
| internal_0_K | 135.0 |
| internal_0_GTP | 3.0 |
| internal_0_ATP | 4.0 |
| internal_0_HEPES | 10.0 |
| internal_0_Cl | 24.0 |
| external_0_Mg | 2.5 |
| external_0_Na | 146.0 |
| external_0_K | 2.5 |
| external_0_Cl | 129.1 |
| external_0_Ca | 1.3 |
| external_0_glucose | 11.0 |
Data table listing
| Data Table | Article Title | Authors | Journal | Year | Table needs expert? | Ephys table mentions | Curated by | Times validated |
|---|---|---|---|---|---|---|---|---|
| 1929 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 6 | Shreejoy Tripathy, Ryan Sefidpour, Dawson Born, | 2 |
| 1925 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 2 | 0 | |
| 1926 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 2 | 0 | |
| 1927 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 2 | 0 | |
| 1928 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 0 | None | |
| 1930 | A functional null mutation of SCN1B in a patient with Dravet syndrome. | Patino GA; Claes LR; Lopez-Santiago LF; Slat EA; Dondeti RS; Chen C; O'Malley HA; Gray CB; Miyazaki H; Nukina N; Oyama F; De Jonghe P; Isom LL | J. Neurosci. | 2009 | False | 0 | None |