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Human Mutation
|
September 12, 2000
A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene
H H Seydewitz, T Gonska, M Mall, et al.
Fortschritte Der Medizin
|
March 29, 1979
[Legal abortion. A prospective study by the Sociomedical Department of the University Clinic for Obstetrics and Gynecology of Basel]
M Mall-Haefeli, T Pfund, U Rauchfleisch, et al.
Geburtshilfe Und Frauenheilkunde
|
January 1, 1991
[Clinical experience with Mercilon and Marvelon with special reference to ovarian function]
M Mall-Haefeli, I Werner-Zodrow, P R Huber
Archiv Fur Gynakologie
|
November 29, 1977
Morphologic alterations in the epithelium of the human oviduct induced by a low dosis gestagen
U M Spornitz, K S Ludwig, M Mall-Haefeli
Therapeutische Umschau. Revue Therapeutique
|
July 1, 1984
[Contraception with the intrauterine pessary: risk of pelvic inflammatory disease]
C Alder, J Bitzer, M Stöcklin, et al.
Schweizer Archiv Fur Neurologie, Neurochirurgie Und Psychiatrie = Archives Suisses De Neurologie, Neurochirurgie Et De Psychiatrie
|
January 1, 1983
[Comparative socioeconomic, anamnestic and psychological studies of patients with uterine myoma and uterine prolapse]
M Fellmann, R Battegay, U Rauchfleisch, et al.
The Journal of Clinical Investigation
|
July 3, 1998
The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways
M Mall, M Bleich, R Greger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1999
The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel
R Schreiber, A Hopf, M Mall, et al.
EMBO Reports
|
October 19, 2001
The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration
J König, R Schreiber, T Voelcker, et al.
The Journal of Biological Chemistry
|
May 13, 1999
Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations
A Hopf, R Schreiber, M Mall, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 87) with videos related to
Sort By:
Page
of 9
Human Mutation
|
September 12, 2000
A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene
H H Seydewitz, T Gonska, M Mall, et al.
Fortschritte Der Medizin
|
March 29, 1979
[Legal abortion. A prospective study by the Sociomedical Department of the University Clinic for Obstetrics and Gynecology of Basel]
M Mall-Haefeli, T Pfund, U Rauchfleisch, et al.
Geburtshilfe Und Frauenheilkunde
|
January 1, 1991
[Clinical experience with Mercilon and Marvelon with special reference to ovarian function]
M Mall-Haefeli, I Werner-Zodrow, P R Huber
Archiv Fur Gynakologie
|
November 29, 1977
Morphologic alterations in the epithelium of the human oviduct induced by a low dosis gestagen
U M Spornitz, K S Ludwig, M Mall-Haefeli
Therapeutische Umschau. Revue Therapeutique
|
July 1, 1984
[Contraception with the intrauterine pessary: risk of pelvic inflammatory disease]
C Alder, J Bitzer, M Stöcklin, et al.
Schweizer Archiv Fur Neurologie, Neurochirurgie Und Psychiatrie = Archives Suisses De Neurologie, Neurochirurgie Et De Psychiatrie
|
January 1, 1983
[Comparative socioeconomic, anamnestic and psychological studies of patients with uterine myoma and uterine prolapse]
M Fellmann, R Battegay, U Rauchfleisch, et al.
The Journal of Clinical Investigation
|
July 3, 1998
The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways
M Mall, M Bleich, R Greger, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1999
The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel
R Schreiber, A Hopf, M Mall, et al.
EMBO Reports
|
October 19, 2001
The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration
J König, R Schreiber, T Voelcker, et al.
The Journal of Biological Chemistry
|
May 13, 1999
Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations
A Hopf, R Schreiber, M Mall, et al.
Page
of 9