S. Diener

发表

Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome.

T. Wieland, T. Meitinger, T. Strom, 2014, The New England journal of medicine.

Loss of cooperativity of secreted CD40L and increased dose–response to IL4 on CLL cell viability correlates with enhanced activation of NF‐kB and STAT6

H. Döhner, K. Rippe, N. Bhattacharya, 2015, International journal of cancer.

Morphologic analysis of human lymphokine‐activated killer (LAK) cells

R. Stahel, H. Hengartner, L. Jost, 1990, International journal of cancer.

SYK carries no activating point mutations in patients with chronic lymphocytic leukaemia (CLL)

H. Döhner, S. Stilgenbauer, T. Zenz, 2010, British journal of haematology.

University of Birmingham Constitutive activation of PKA catalytic subunit in Adrenal Cushing's Syndrome

F. Faucz, F. Beuschlein, M. Lohse, 2014 .

Development of A Cell-Based Assay to Identify Small Molecule Inhibitors of FGF23 Signaling.

T. Strom, Kenji Schorpp, K. Hadian, 2015, Assay and drug development technologies.

Molecular Genetics of Phosphate Homeostasis

S. Diener, 2015 .

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia

Gerhard K. H. Przemeck, H. Fuchs, T. Wieland, 2016, Mammalian Genome.

An ENU mutagenesis-derived mouse model with a dominant Jak1 mutation resembling phenotypes of systemic autoimmune disease.

H. Fuchs, D. Busch, H. Höfler, 2013, The American journal of pathology.

Frequency and clinical correlates of somatic Ying Yang 1 mutations in sporadic insulinomas.

T. Wieland, T. Meitinger, T. Strom, 2015, The Journal of clinical endocrinology and metabolism.

Nurse‐like cells show deregulated expression of genes involved in immunocompetence

H. Döhner, H. Busch, N. Bhattacharya, 2011, British journal of haematology.

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations

Gerhard K. H. Przemeck, H. Fuchs, D. Busch, 2016, G3: Genes, Genomes, Genetics.

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

T. Wieland, T. Meitinger, T. Strom, 2013, Nature Genetics.

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia

Gerhard K. H. Przemeck, H. Fuchs, T. Wieland, 2016, Mammalian Genome.

Non-malignant B cells and chronic lymphocytic leukemia cells induce a pro-survival phenotype in CD14+ cells from peripheral blood

H. Döhner, N. Bhattacharya, S. Stilgenbauer, 2011, Leukemia.

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations

Gerhard K. H. Przemeck, H. Fuchs, D. Busch, 2016, G3: Genes, Genomes, Genetics.