Ines Müller
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Monoclonal and Polyclonal Antibodies Research, Advanced Proteomics Techniques and Applications, Glycosylation and Glycoproteins Research, Cell death mechanisms and regulation
Most-Cited Works
- → Lack of beta-arrestin signaling in the absence of active G proteins(2018)367 cited
- → Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation(2007)287 cited
- → Intracerebral accumulation of glutaric and 3‐hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl‐CoA dehydrogenase deficiency(2006)163 cited
- → Neurodegeneration and chronic renal failure in methylmalonic aciduria—A pathophysiological approach(2007)130 cited
- → The Genomic Sequence and Comparative Analysis of the Rat Major Histocompatibility Complex(2004)121 cited
- → Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum(2014)113 cited
- → The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation(2004)95 cited
- → Cancer Cells Employ Nuclear Caspase-8 to Overcome the p53-Dependent G2/M Checkpoint through Cleavage of USP28(2020)84 cited
- → CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X‐linked infantile spasm syndrome(2009)80 cited
- → The genome of Erwinia tasmaniensis strain Et1/99, a non‐pathogenic bacterium in the genus Erwinia(2008)79 cited