Birgit Mentrup - Publications

Novel molecular cues for dental defects in hypophosphatasia.

Journal: Experimental cell research

Published: December 19, 2019

Modulation of Transient Receptor Potential Channels 3 and 6 Regulates Osteoclast Function with Impact on Trabecular Bone Loss.

Journal: Calcified tissue international

Published: November 19, 2019

A Fosmid Pool-Based Next Generation Sequencing Approach to Haplotype-Resolve Whole Genomes.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: February 01, 2017

Low-energy trauma-induced intercondylar femoral fracture.

Journal: Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases

Published: December 07, 2016

Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells.

Journal: Scientific reports

Published: October 28, 2016

A homozygous intronic branch-point deletion in the ALPL gene causes infantile hypophosphatasia.

Journal: Bone

Published: August 03, 2016

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

Journal: Mammalian genome : official journal of the International Mammalian Genome Society

Published: October 01, 2015

Recombinant Enzyme Replacement Therapy in Hypophosphatasia.

Journal: Sub-cellular biochemistry

Published: July 30, 2015

Overexpression of tissue-nonspecific alkaline phosphatase increases the expression of neurogenic differentiation markers in the human SH-SY5Y neuroblastoma cell line.

Journal: Bone

Published: January 22, 2015

Probenecid as a sensitizer of bisphosphonate-mediated effects in breast cancer cells.

Journal: Molecular cancer

Published: January 29, 2014

Unexpected high intrafamilial phenotypic variability observed in hypophosphatasia.

Journal: European journal of human genetics : EJHG

Published: October 01, 2013

Compound heterozygosity of two functional null mutations in the ALPL gene associated with deleterious neurological outcome in an infant with hypophosphatasia.

Journal: Bone

Published: October 16, 2012