apl. Prof. Dr. Elisabeth Sock



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Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

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To

Abstract

Journal

Analysis of the human SOX10 mutation Q377X in mice and its implications for genotype-phenotype correlation in SOX10-related human disease. (2018) Truch K, Arter J, Turnescu T, Weider M, Hartwig A, Tamm ER, Sock E, Wegner M Journal article Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT). (2018) Neirijnck Y, Reginensi A, Renkema KY, Massa F, Kozlov VM, Dhib H, Bongers EMHF, et al. Journal article, Original article The role of zinc finger transcription factor Zfp276 during glial development (2017) Küspert M, Sock E, Wegner M Conference contribution Sp2 is the only glutamine-rich Specificity protein with minor impact on development and differentiation in myelinating glia. (2017) Wegener A, Küspert M, Sock E, Philipsen S, Suske G, Wegner M Journal article, Original article The Dual-specificity phosphatase Dusp15 is regulated by Sox10 and Myrf in Myelinating Oligodendrocytes (2016) Muth K, Piefke S, Weider M, Sock E, Hermans-Borgmeyer I, Wegner M, Küspert M Journal article Sox5 controls dorsal progenitor and interneuron specification in the spinal cord (2015) Quiroga AC, Stolt C, Diez Del Corral R, Dimitrov S, Perez-Alcala S, Sock E, Barbas JA, et al. Journal article Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development (2015) Kim GJ, Sock E, Buchberger A, Just W, Denzer F, Hoepffner W, German J, et al. Journal article Orchestration of Neuronal Differentiation and Progenitor Pool Expansion in the Developing Cortex by SoxC Genes (2015) Chen C, Lee GA, Pourmorady A, Sock E, Donoghue MJ Journal article Cardiac outflow tract development relies on the complex function of Sox4 and Sox11 in multiple cell types (2014) Paul M, Harvey RP, Wegner M, Sock E Journal article Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia (2014) Perez-Branguli F, Mishra HK, Prots I, Havlicek S, Kohl Z, Saul D, Rummel C, et al. Journal article
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