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Nucleic Acids Research
|
February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies
F Degoul, I Nelson, S Amselem, et al.
Biochemical and Biophysical Research Communications
|
June 29, 1990
Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR
B Obermaier-Kusser, J Müller-Höcker, I Nelson, et al.
Diabetes
|
November 1, 1991
Prevention by protein kinase C inhibitors of glucose-induced insulin-receptor tyrosine kinase resistance in rat fat cells
H K Müller, M Kellerer, B Ermel, et al.
The Journal of Biological Chemistry
|
June 5, 1989
A defective intramolecular autoactivation cascade may cause the reduced kinase activity of the skeletal muscle insulin receptor from patients with non-insulin-dependent diabetes mellitus
B Obermaier-Kusser, M F White, D E Pongratz, et al.
Biochemistry
|
May 19, 1992
Distinct alpha-subunit structures of human insulin receptor A and B variants determine differences in tyrosine kinase activities
M Kellerer, R Lammers, B Ermel, et al.
The Biochemical Journal
|
August 1, 1989
Further evidence for a two-step model of glucose-transport regulation. Inositol phosphate-oligosaccharides regulate glucose-carrier activity
B Obermaier-Kusser, C Mühlbacher, J Mushack, et al.
The Biochemical Journal
|
May 15, 1991
Insulin activates GTP binding to a 40 kDa protein in fat cells
M Kellerer, B Obermaier-Kusser, A Pröfrock, et al.
FEBS Letters
|
July 29, 1991
Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))]
B Obermaier-Kusser, I Paetzke-Brunner, C Enter, et al.
Diabetologia
|
May 1, 1992
Subcellular distribution of GLUT 4 in the skeletal muscle of lean type 2 (non-insulin-dependent) diabetic patients in the basal state
B Vogt, C Mühlbacher, J Carrascosa, et al.
Human Genetics
|
December 1, 1991
A specific point mutation in the mitochondrial genome of Caucasians with MELAS
C Enter, J Müller-Höcker, S Zierz, et al.
Page
of 7
Search research articles
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Showing results (41-50 of 67) with videos related to
Sort By:
Page
of 7
Nucleic Acids Research
|
February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies
F Degoul, I Nelson, S Amselem, et al.
Biochemical and Biophysical Research Communications
|
June 29, 1990
Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR
B Obermaier-Kusser, J Müller-Höcker, I Nelson, et al.
Diabetes
|
November 1, 1991
Prevention by protein kinase C inhibitors of glucose-induced insulin-receptor tyrosine kinase resistance in rat fat cells
H K Müller, M Kellerer, B Ermel, et al.
The Journal of Biological Chemistry
|
June 5, 1989
A defective intramolecular autoactivation cascade may cause the reduced kinase activity of the skeletal muscle insulin receptor from patients with non-insulin-dependent diabetes mellitus
B Obermaier-Kusser, M F White, D E Pongratz, et al.
Biochemistry
|
May 19, 1992
Distinct alpha-subunit structures of human insulin receptor A and B variants determine differences in tyrosine kinase activities
M Kellerer, R Lammers, B Ermel, et al.
The Biochemical Journal
|
August 1, 1989
Further evidence for a two-step model of glucose-transport regulation. Inositol phosphate-oligosaccharides regulate glucose-carrier activity
B Obermaier-Kusser, C Mühlbacher, J Mushack, et al.
The Biochemical Journal
|
May 15, 1991
Insulin activates GTP binding to a 40 kDa protein in fat cells
M Kellerer, B Obermaier-Kusser, A Pröfrock, et al.
FEBS Letters
|
July 29, 1991
Respiratory chain activity in tissues from patients (MELAS) with a point mutation of the mitochondrial genome [tRNA(Leu(UUR))]
B Obermaier-Kusser, I Paetzke-Brunner, C Enter, et al.
Diabetologia
|
May 1, 1992
Subcellular distribution of GLUT 4 in the skeletal muscle of lean type 2 (non-insulin-dependent) diabetic patients in the basal state
B Vogt, C Mühlbacher, J Carrascosa, et al.
Human Genetics
|
December 1, 1991
A specific point mutation in the mitochondrial genome of Caucasians with MELAS
C Enter, J Müller-Höcker, S Zierz, et al.
Page
of 7