F. Brand

发表

Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)

M. Klintschar, A. Kispert, D. Haffner, 2015, Human Genetics.

Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2

R. Geffers, Z. Gucev, V. Tasic, 2022, Human Genetics.

Rare heterozygous GDF6 variants in patients with renal anomalies

R. Geffers, Z. Gucev, V. Tasic, 2020, European Journal of Human Genetics.

Structural requirements of alloxan and ninhydrin for glucokinase inhibition and of glucose for protection against inhibition

S. Lenzen, U. Panten, F. Brand, 1988, British journal of pharmacology.

Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations

A. Kispert, D. Haffner, L. Pape, 2017, Human Molecular Genetics.

Rare ADAR and RNASEH2B variants and a type I interferon signature in glioma and prostate carcinoma risk and tumorigenesis

Martin A. M. Reijns, G. Reifenberger, M. Weller, 2017, Acta Neuropathologica.

FOCAD loss impacts microtubule assembly, G2/M progression and patient survival in astrocytic gliomas

G. Reifenberger, M. Weller, M. Westphal, 2019, Acta Neuropathologica.

Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)

M. Klintschar, A. Kispert, D. Haffner, 2015, Human Genetics.

Adenosine A(2A) receptor dynamics studied with the novel fluorescent agonist Alexa488-APEC.

B. Fredholm, G. Schulte, K. Jacobson, 2008, European journal of pharmacology.

Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients

F. Feuerhake, P. Andersen, S. Petri, 2021, Genes.

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin

J. Krauss, A. Samii, C. Hartmann, 2021, Acta Neuropathologica.

Regulation and function of ERK3/MK5-mediated signaling

F. Brand, 2012 .

A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics

S. Petri, A. Das, B. Auber, 2022, Journal of Neurology.

The Extracellular Signal-Regulated Kinase 3 (Mitogen-Activated Protein Kinase 6 [MAPK6])–MAPK-Activated Protein Kinase 5 Signaling Complex Regulates Septin Function and Dendrite Morphology

M. Gaestel, S. Meloche, S. Schumacher, 2012, Molecular and Cellular Biology.

Function and Dendrite Morphology 5 Signaling Complex Regulates Septin MAPK-Activated Protein Kinase − [ MAPK 6 ] ) ( Mitogen-Activated Protein Kinase 6 The Extracellular Signal-Regulated Kinase 3

M. Gaestel, S. Meloche, S. Schumacher, 2012 .

Brand „ Agonist-induced Signaling and Endocytosis of the Adenosine A 2 A Receptor “

G. Schulte, F. Brand, 2007 .