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Journal of Neurology|November 18, 2000
PMP22 Thr118Met is not a clinically relevant CMT1 markerP Young, F Stögbauer, B Eller, et al.
Scientific Reports|February 24, 2016
Monocyte-induced recovery of inflammation-associated hepatocellular dysfunction in a biochip-based human liver modelMarko Gröger, Knut Rennert, Benjamin Giszas, et al.
Scientific Reports|May 15, 2018
Corrigendum: Monocyte-induced recovery of inflammation-associated hepatocellular dysfunction in a biochip-based human liver modelMarko Gröger, Knut Rennert, Benjamin Giszas, et al.
Scientific Reports|November 27, 2025
Brain power comparison between microgravity and head-down tilt bed rest: an electroencephalography approachMaría Sevilla-García, Adrián Quivira-Lopesino, Pablo Cuesta, et al.
Human Molecular Genetics|July 21, 2009
Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceGo Suzuki, Kathryn M Harper, Takeshi Hiramoto, et al.
International Journal of Molecular Medicine|January 16, 2014
The (pro)renin receptor mediates constitutive PLZF-independent pro-proliferative effects which are inhibited by bafilomycin but not genisteinSebastian Kirsch, Eva Schrezenmeier, Sabrina Klare, et al.
American Journal of Human Genetics|February 12, 2011
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathyDaniel M Jordan, Adam Kiezun, Samantha M Baxter, et al.
Schmerz (Berlin, Germany)|June 30, 2017
[What does pain intensity mean from the patient perspective? : A qualitative study on the patient perspective of pain intensity as an outcome parameter in treatment evaluation and on the interpretability of pain intensity measurements]K Neustadt, S Deckert, C Kopkow, et al.
Arquivos De Neuro-Psiquiatria|October 25, 2008
Neurological complications of hematopoietic stem cell transplantation (HSCT): a retrospective study in a HSCT center in BrazilHélio A G Teive, Vaneuza Funke, Marco A Bitencourt, et al.
Human Molecular Genetics|November 16, 2001
Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defectsB Funke, J A Epstein, L K Kochilas, et al.
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