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Results: 1-25/32
Authors:
Betz, RC
Schoser, BGH
Kasper, D
Ricker, K
Ramirez, A
Stein, V
Torbergsen, T
Lee, YA
Nothen, MM
Wienker, TF
Malin, JP
Propping, P
Reis, A
Mortier, W
Jentsch, TJ
Vorgerd, M
Kubisch, C
Citation: Rc. Betz et al., Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle inrippling muscle disease, NAT GENET, 28(3), 2001, pp. 218-219
Authors:
Hubner, CA
Stein, V
Hermans-Borgmeyer, I
Meyer, T
Ballanyi, K
Jentsch, TJ
Citation: Ca. Hubner et al., Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibition, NEURON, 30(2), 2001, pp. 515-524
Authors:
Stobrawa, SM
Breiderhoff, T
Takamori, S
Engel, D
Schweizer, M
Zdebik, AA
Bosl, MR
Ruether, K
Jahn, H
Draguhn, A
Jahn, R
Jentsch, TJ
Citation: Sm. Stobrawa et al., Disruption of CIC-3, a chloride channel expressed on synaptic vesicles, leads to a loss of the hippocampus, NEURON, 29(1), 2001, pp. 185-196
Authors:
Vandewalle, A
Cluzeaud, F
Peng, KC
Bens, M
Luchow, A
Gunther, W
Jentsch, TJ
Citation: A. Vandewalle et al., Tissue distribution and subcellular localization of the ClC-5 chloride channel in rat intestinal cells, AM J P-CELL, 280(2), 2001, pp. C373-C381
Authors:
Bosl, MR
Stein, V
Hubner, C
Zdebik, AA
Jordt, SE
Mukhopadhyay, AK
Davidoff, MS
Holstein, AF
Jentsch, TJ
Citation: Mr. Bosl et al., Male germ cells and photoreceptors, both dependent on close cell-cell interactions, degenerate upon ClC-2Cl(-) channel disruption, EMBO J, 20(6), 2001, pp. 1289-1299
Authors:
Kornak, U
Kasper, D
Bosl, MR
Kaiser, E
Schweizer, M
Schulz, A
Friedrich, W
Delling, G
Jentsch, TJ
Citation: U. Kornak et al., Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man, CELL, 104(2), 2001, pp. 205-215
Authors:
Estevez, R
Bottger, T
Stein, V
Birkenhager, R
Otto, E
Hildebrandt, F
Jentsch, TJ
Citation: R. Estevez et al., Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion, NATURE, 414(6863), 2001, pp. 558-561
Authors:
Dedek, K
Kunath, B
Kananura, C
Reuner, U
Jentsch, TJ
Steinlein, OK
Citation: K. Dedek et al., Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel, P NAS US, 98(21), 2001, pp. 12272-12277
Authors:
Weinreich, F
Jentsch, TJ
Citation: F. Weinreich et Tj. Jentsch, Pores formed by single subunits in mixed dimers of different CLC chloride channels, J BIOL CHEM, 276(4), 2001, pp. 2347-2353
Authors:
Schwake, M
Friedrich, T
Jentsch, TJ
Citation: M. Schwake et al., An internalization signal in ClC-5, an endosomal Cl- channel mutated in Dent's disease, J BIOL CHEM, 276(15), 2001, pp. 12049-12054
Authors:
Jentsch, TJ
Citation: Tj. Jentsch, Neuronal KCNQ potassium channels: Physiology and role in disease, NAT REV NEU, 1(1), 2000, pp. 21-30
Authors:
Yamamoto, K
Cox, JPDT
Friedrich, T
Christie, PT
Bald, M
Houtman, PN
Lapsley, MJ
Patzer, L
Tsimaratos, M
Van't Hoff, WG
Yamaoka, K
Jentsch, TJ
Thakker, RV
Citation: K. Yamamoto et al., Characterization of renal chloride channel (CLCN5) mutations in Dent's disease, J AM S NEPH, 11(8), 2000, pp. 1460-1468
Authors:
Waldegger, S
Jentsch, TJ
Citation: S. Waldegger et Tj. Jentsch, From tonus to tonicity: Physiology of CLC chloride channels, J AM S NEPH, 11(7), 2000, pp. 1331-1339
Authors:
Kornak, U
Schulz, A
Friedrich, W
Uhlhaas, S
Kremens, B
Voit, T
Hasan, C
Bode, U
Jentsch, TJ
Kubisch, C
Citation: U. Kornak et al., Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis, HUM MOL GEN, 9(13), 2000, pp. 2059-2063
Authors:
Weinreich, F
Jentsch, TJ
Citation: F. Weinreich et Tj. Jentsch, Neurological diseases caused by ion-channel mutations, CUR OP NEUR, 10(3), 2000, pp. 409-415
Authors:
Piwon, N
Gunther, W
Schwake, M
Bosl, MR
Jentsch, TJ
Citation: N. Piwon et al., CIC-5Cl(-)-channel disruption impairs endocytosis in a mouse model for Dent's disease, NATURE, 408(6810), 2000, pp. 369-373
Authors:
Jentsch, TJ
Citation: Tj. Jentsch, Ion channels and disease, NATURE, 406(6793), 2000, pp. 236-237
Authors:
Schroeder, BC
Waldegger, S
Fehr, S
Bleich, M
Warth, R
Greger, R
Jentsch, TJ
Citation: Bc. Schroeder et al., A constitutively open potassium channel formed by KCNQ1 and KCNE3, NATURE, 403(6766), 2000, pp. 196-199
Authors:
Kharkovets, T
Hardelin, JP
Safieddine, S
Schweizer, M
El-Amraoui, A
Petit, C
Jentsch, TJ
Citation: T. Kharkovets et al., KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway, P NAS US, 97(8), 2000, pp. 4333-4338
Authors:
Selyanko, AA
Hadley, JK
Wood, IC
Abogadie, FC
Jentsch, TJ
Brown, DA
Citation: Aa. Selyanko et al., Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M-1 muscarinic acetylcholine receptors, J PHYSL LON, 522(3), 2000, pp. 349-355
Authors:
Waldegger, S
Jentsch, TJ
Citation: S. Waldegger et Tj. Jentsch, Functional and structural analysis of ClC-K chloride channels involved in renal disease, J BIOL CHEM, 275(32), 2000, pp. 24527-24533
Authors:
Schroeder, BC
Hechenberger, M
Weinreich, F
Kubisch, C
Jentsch, TJ
Citation: Bc. Schroeder et al., KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents, J BIOL CHEM, 275(31), 2000, pp. 24089-24095
Authors:
Schwake, M
Pusch, M
Kharkovets, T
Jentsch, TJ
Citation: M. Schwake et al., Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K+channels involved in epilepsy, J BIOL CHEM, 275(18), 2000, pp. 13343-13348
Authors:
Jentsch, TJ
Schroeder, BC
Kubisch, C
Friedrich, T
Stein, V
Citation: Tj. Jentsch et al., Pathophysiology of KCNQ channels: Neonatal epilepsy and progressive deafness, EPILEPSIA, 41(8), 2000, pp. 1068-1069
Authors:
Kubisch, C
Schroeder, BC
Friedrich, T
Lutjohann, B
El-Amraoui, A
Marlin, S
Petit, C
Jentsch, TJ
Citation: C. Kubisch et al., KCNQ4, a novel potassium channel expressed in sensory outer hair cells, ismutated in dominant deafness, CELL, 96(3), 1999, pp. 437-446