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Pain|October 9, 2024
Na V 1.8/Na V 1.9 double deletion mildly affects acute pain responses in miceMarta Alves-Simões, Laura Teege, Cecilia Tomni, et al.
The Journal of Clinical Investigation|January 9, 2019
DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humansGergely Karsai, Florian Kraft, Natja Haag, et al.
Scientific Reports|March 26, 2021
The difficulty to model Huntington's disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cellsKim Le Cann, Alec Foerster, Corinna Rösseler, et al.
The Journal of Biological Chemistry|June 10, 2009
Rdh12 activity and effects on retinoid processing in the murine retinaJared D Chrispell, Kecia L Feathers, Maureen A Kane, et al.
Nature|June 5, 2015
Regulation of endoplasmic reticulum turnover by selective autophagyAliaksandr Khaminets, Theresa Heinrich, Muriel Mari, et al.
International Journal of Molecular Sciences|August 3, 2019
Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver FibrosisTheresa Hildegard Wirtz, Petra Fischer, Christina Backhaus, et al.
Nature Genetics|October 20, 2009
Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathyIngo Kurth, Torsten Pamminger, J Christopher Hennings, et al.
Ebiomedicine|December 4, 2018
Pain relief in a neuropathy patient by lacosamide: Proof of principle of clinical translation from patient-specific iPS cell-derived nociceptorsBarbara Namer, Diana Schmidt, Esther Eberhardt, et al.
European Journal of Human Genetics : EJHG|August 20, 2021
Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disabilityNatja Haag, Ene-Choo Tan, Matthias Begemann, et al.
American Journal of Human Genetics|October 7, 2008
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndromeHyung-Goo Kim, Ingo Kurth, Fei Lan, et al.
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