Kathrin Huehne

Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy

Jan Senderek, Carsten Bergmann, Claudia Stendel et al. · The American Journal of Human Genetics · 2003 · 210 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mendelian Disorder +9

Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models

Alejandro Leal, Kathrin Huehne, Finn Bauer et al. · Neurogenetics · 2009 · 80 citations · Full text

Engineering, Pmp22 Rna Levels, Genetics +20

Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations

Knut Brockmann, Steffi Dreha‐Kulaczewski, Peter Dechent et al. · Journal of Neurology · 2008 · 72 citations · Full text

Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia

Jin‐Sung Choi, Xiaoyang Cheng, Edmund Foster et al. · Brain · 2010 · 68 citations

Characterization of a New Bacteriocin Operon in Sakacin P-Producing<i>Lactobacillus sakei</i>, Showing Strong Translational Coupling between the Bacteriocin and Immunity Genes

Geir Mathiesen, Kathrin Huehne, Lothar Kroeckel et al. · Applied and Environmental Microbiology · 2005 · 67 citations · Full text