UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 848

Sortiert nach

Neuronal KCNQ potassium channels: physiology and role in disease

Nature reviews. Neuroscience, 2000-10, Vol.1 (1), p.21-30

Jentsch, T J

2000

Volltextzugriff (PDF)

A Potassium Channel Mutation in Neonatal Human Epilepsy

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5349), p.403-406

1998

Volltextzugriff (PDF)

Chloride channel diseases resulting from impaired transepithelial transport or vesicular function

The Journal of clinical investigation, 2005-08, Vol.115 (8), p.2039-2046

2005

Volltextzugriff (PDF)

ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion

Bone (New York, N.Y.), 2014-01, Vol.58, p.92-102

2014

Volltextzugriff (PDF)

A constitutively open potassium channel formed by KCNQ1 and KCNE3

Nature (London), 2000-01, Vol.403 (6766), p.196-199

2000

Volltextzugriff (PDF)

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K + channels causes epilepsy

Nature (London), 1998-12, Vol.396 (6712), p.687-690

1998

Volltextzugriff (PDF)

Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis

Human molecular genetics, 2000-08, Vol.9 (13), p.2059-2063

2000

Volltextzugriff (PDF)

The CLC chloride channel family

Pflügers Archiv, 1999-05, Vol.437 (6), p.783-795

1999

Volltextzugriff (PDF)

Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses

Neuroscience, 2007-11, Vol.149 (3), p.673-684

2007

Volltextzugriff (PDF)

Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

Human molecular genetics, 1997-10, Vol.6 (11), p.1943-1949

1997

Volltextzugriff (PDF)

Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (21), p.12272-12277

2001

Volltextzugriff (PDF)

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

The Journal of physiology, 2000-02, Vol.522 (3), p.349-355

2000

Volltextzugriff (PDF)

Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease

The Journal of biological chemistry, 2000-08, Vol.275 (32), p.24527-24533

2000

Volltextzugriff (PDF)

Two physically distinct pores in the dimeric CIC-0 chloride channel

Nature (London), 1996-09, Vol.383 (6598), p.340-343

1996

Volltextzugriff (PDF)

A common molecular basis for three inherited kidney stone diseases

Nature (London), 1996-02, Vol.379 (6564), p.445-449

1996

Volltextzugriff (PDF)

Localization and induction by dehydration of ClC-K chloride channels in the rat kidney

American journal of physiology. Renal physiology, 1997-05, Vol.272 (5), p.678-F688

1997

Volltextzugriff (PDF)

Properties of voltage-gated chloride channels of the ClC gene family

The Journal of physiology, 1995-01, Vol.482 (P), p.19S-25

1995

Volltextzugriff (PDF)

Reply from L. P. Cid, T. J. Jentsch and F. V. Sepúlveda: intestinal electrolyte and fluid secretion – a model in trouble?

The Journal of physiology, 2018-06, Vol.596 (12), p.2465-2466

2018

Volltextzugriff (PDF)

ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence

Human molecular genetics, 1998-10, Vol.7 (11), p.1753-1760

1998

Volltextzugriff (PDF)

ClC-5 Cl - -channel disruption impairs endocytosis in a mouse model for Dent's disease

Nature (London), 2000-11, Vol.408 (6810), p.369-373

2000

Volltextzugriff (PDF)

The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Science (American Association for the Advancement of Science), 1992-08, Vol.257 (5071), p.797-800

1992

Volltextzugriff (PDF)

Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

Nature (London), 1991-11, Vol.354 (6351), p.301-304

1991

Volltextzugriff (PDF)

Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

Nature (London), 1990-12, Vol.348 (6301), p.510-514

1990

Volltextzugriff (PDF)

Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions

The Journal of general physiology, 1998-05, Vol.111 (5), p.653-665

1998

Volltextzugriff (PDF)

1 – 25 von 848

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(762)
Mit Volltextzugriff
(774)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(517)
Life Sciences & Biomedicine
(434)
Animals
(332)
Humans
(227)
Biological And Medical Sciences
(158)
Male
(148)
Neurosciences
(134)
Neurosciences & Neurology
(133)
Female
(120)
Mice
(119)
Biochemistry & Molecular Biology
(94)
Fundamental And Applied Biological Sciences. Psychology
(86)
Chloride Channels - Genetics
(84)
Medical Sciences
(83)
Mutation
(79)
Rats
(70)
Chloride Channels - Metabolism
(67)
Molecular Sequence Data
(65)
Cell Biology
(60)
Amino Acid Sequence
(59)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Neuronal KCNQ potassium channels: physiology and role in disease

A Potassium Channel Mutation in Neonatal Human Epilepsy

Chloride channel diseases resulting from impaired transepithelial transport or vesicular function

ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion

A constitutively open potassium channel formed by KCNQ1 and KCNE3

Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K + channels causes epilepsy

Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis

The CLC chloride channel family

Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses

Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel

Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors

Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease

Two physically distinct pores in the dimeric CIC-0 chloride channel

A common molecular basis for three inherited kidney stone diseases

Localization and induction by dehydration of ClC-K chloride channels in the rat kidney

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

Properties of voltage-gated chloride channels of the ClC gene family

Reply from L. P. Cid, T. J. Jentsch and F. V. Sepúlveda: intestinal electrolyte and fluid secretion – a model in trouble?

ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence

ClC-5 Cl - -channel disruption impairs endocytosis in a mouse model for Dent's disease

The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

Primary structure and functional expression of a developmentally regulated skeletal muscle chloride channel

Primary structure of Torpedo marmorata chloride channel isolated by expression cloning in Xenopus oocytes

Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions

Suchergebnisse filtern