I. Aukrust
发表
Amy L. Williams,
T. Fennell,
S. Gabriel,
2014,
JAMA.
I. Aukrust,
J. Saraste,
A. Vedeler,
2017,
FEBS open bio.
P. Njølstad,
K. Hussain,
Z. Šumník,
2015,
The Journal of clinical endocrinology and metabolism.
G. Houge,
K. Teigen,
I. Aukrust,
2019,
Ophthalmic genetics.
W. Sjursen,
P. Knappskog,
M. Van Ghelue,
2022,
Familial Cancer.
T. Flatmark,
G. Travé,
R. Atkinson,
2006,
Journal of molecular biology.
R. Pfundt,
S. Mehta,
M. Roselló,
2017,
European Journal of Human Genetics.
T. Flatmark,
I. Aukrust,
A. Døskeland,
2005,
FEBS letters.
P. Njølstad,
I. Aukrust,
L. Bjørkhaug,
2020,
The Journal of clinical endocrinology and metabolism.
P. Njølstad,
I. Aukrust,
L. Bjørkhaug,
2018,
Scientific Reports.
P. Njølstad,
T. Flatmark,
N. Wierup,
2017,
Molecular and Cellular Endocrinology.
A. Molven,
P. Njølstad,
T. Arnesen,
2020,
Journal of inherited metabolic disease.
Michael H. Preuss,
A. Gloyn,
R. Loos,
2022,
Diabetologia.
A. Molven,
P. Njølstad,
O. Søvik,
2012,
Biochimica et biophysica acta.
P. Dawson,
A. Molven,
E. Tjora,
2022,
JPGN reports.
A. Ferbert,
B. Wirth,
B. H. Eriksen,
2017,
European Journal of Human Genetics.
E. Zeggini,
T. Hansen,
N. Grarup,
2022,
The Lancet regional health. Europe.
G. Houge,
P. Knappskog,
S. Berland,
2017,
Acta ophthalmologica.
R. Stevenson,
A. Barkovich,
H. Warren,
2020,
Journal of Medical Genetics.
D. Altshuler,
L. Groop,
J. Flannick,
2016,
Diabetes.
T. Flatmark,
E. Strand,
I. Aukrust,
2006,
Biochimica et biophysica acta.
M. McCarthy,
S. Ellard,
A. Mahajan,
2020,
American journal of human genetics.
M. McCarthy,
S. Ellard,
A. Gloyn,
2019,
medRxiv.
Adam Kiezun,
Sergio Islas-Andrade,
Pierre Fontanillas,
2016
.
I. Cristea,
O. Bruland,
E. Rødahl,
2021,
FEBS letters.
S. Gygi,
P. Njølstad,
O. Søvik,
2013,
The Journal of Biological Chemistry.
K. Yamakawa,
A. Takata,
N. Matsumoto,
2018,
European Journal of Human Genetics.
M. Reijnders,
W. Chung,
A. Munnich,
2020,
Genetics in Medicine.
S. Johansson,
B. Thompson,
P. James,
2021,
International journal of molecular sciences.
S. Levy,
A. Molven,
P. Njølstad,
2017,
Diabetologia.
O. Bruland,
P. Knappskog,
S. Berland,
2020,
Acta ophthalmologica.
T. Arnesen,
G. Houge,
L. M. Myklebust,
2018,
BMC medical genetics.
T. Flatmark,
G. Travé,
E. Strand,
2007,
Journal of molecular biology.
W. Sjursen,
P. Knappskog,
M. Van Ghelue,
2023,
Genes.
P. Njølstad,
O. Søvik,
T. Flatmark,
2011,
The FEBS journal.
Kristin A. Maloney,
K. Owen,
A. Gloyn,
2023,
medRxiv.
S. Johansson,
P. Knappskog,
W. Norton,
2021,
Frontiers in Molecular Neuroscience.
P. Njølstad,
O. Søvik,
T. Flatmark,
2014,
Molecular and Cellular Endocrinology.
GCK-MODY diabetes as a protein misfolding disease : The mutation R 275 C promotes protein misfolding
P. Njølstad,
O. Søvik,
T. Flatmark,
2013
.
K. Yamakawa,
A. Takata,
N. Matsumoto,
2018,
European Journal of Human Genetics.
P. Njølstad,
T. Arnesen,
P. Kursula,
2022,
The Journal of biological chemistry.
P. Njølstad,
T. Arnesen,
P. Kursula,
2021,
bioRxiv.
K. Heimdal,
S. Johansson,
O. Bruland,
2014,
Orphanet Journal of Rare Diseases.
K. Heimdal,
S. Johansson,
R. Kleppe,
2017,
Bioscience reports.
R. Pfundt,
S. Mehta,
M. Roselló,
2017,
European Journal of Human Genetics.
P. Knappskog,
M. Van Ghelue,
I. Aukrust,
2023,
BMC Cancer.
Kristin A. Maloney,
K. Owen,
A. Gloyn,
2023,
Communications medicine.
Kristin A. Maloney,
J. Pankow,
L. Redman,
2023,
Nature Medicine.
E. Søfteland,
Eivind Valen,
A. Molven,
2023,
Diabetologia.
D. Ville,
V. Katanaev,
A. Koval,
2023,
Cells.
Kristin A. Maloney,
J. Pankow,
A. Hattersley,
2023,
Communications medicine.