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Irm Hermans-Borgmeyer

University of Hamburg

91

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7415

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Amelioration of the abnormal phenotype of a new L1 syndrome mouse mutation with L1 mimetics.

2021 The FASEB Journal
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Revisiting the proteolytic processing of cell adhesion molecule L1

2020 Journal of Neurochemistry
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Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritis

2020 Osteoarthritis and Cartilage
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Mice Carrying a Ubiquitous R235W Mutation of Wnt1 Display a Bone‐Specific Phenotype

2020 Journal of Bone and Mineral Research
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Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone-specific phenotype

2020 Bone reports
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Segregated expression of ENaC subunits in taste cells

2020 Chemical Senses
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Author response for "Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone‐specific phenotype"

2020
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Spastin depletion increases tubulin polyglutamylation and impairs kinesin-mediated neuronal transport, leading to working and associative memory deficits.

2020 PLOS Biology
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A novel mouse model of phospholipase A2 receptor 1-associated membranous nephropathy mimics podocyte injury in patients

2019 Kidney International
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The Microtubule Severing Protein Katanin Regulates Proliferation of Neuronal Progenitors in Embryonic and Adult Neurogenesis

2019 Scientific Reports
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