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Gudrun Rappold

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Articles 63
Citations 2582
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Recent Articles
1.
Berens S, Dong Y, Fritz N, Walstab J, DAmato M, Zheng T, et al.
World J Gastroenterol . 2022 Jul; 28(21):2334-2349. PMID: 35800179
Background: Single-nucleotide polymorphisms (SNPs) of the serotonin type 3 receptor subunit () genes have been associated with psychosomatic symptoms, but it is not clear whether these associations exist in irritable...
2.
Cossais F, Schaeffer E, Heinzel S, Zimmermann J, Niesler B, Roth R, et al.
J Parkinsons Dis . 2020 Dec; 11(1):171-176. PMID: 33337386
Still little is known about the nature of the gastrointestinal pathological alterations occurring in Parkinson's disease (PD). Here, we used multiplexed mRNA profiling to measure the expression of a panel...
3.
Frohlich H, Kollmeyer M, Linz V, Stuhlinger M, Groneberg D, Reigl A, et al.
Proc Natl Acad Sci U S A . 2019 Oct; 116(44):22237-22245. PMID: 31611379
Gastrointestinal dysfunctions in individuals with autism spectrum disorder are poorly understood, although they are common among this group of patients. haploinsufficiency is characterized by autistic behavior, language impairment, and intellectual...
4.
Eltokhi A, Rappold G, Sprengel R
Front Mol Neurosci . 2018 Aug; 11:240. PMID: 30072871
The SHANK scaffolding proteins are important organizers for signaling proteins in the postsynapse of excitatory neurons. The functional significance of SHANK proteins becomes apparent by the wide spectrum of neurodevelopmental...
5.
Martinez C, Rodino-Janeiro B, Lobo B, Stanifer M, Klaus B, Granzow M, et al.
Gut . 2017 Jan; 66(9):1537-1538. PMID: 28082316
Objective: Micro-RNAs (miRNAs) play a crucial role in controlling intestinal epithelial barrier function partly by modulating the expression of tight junction (TJ) proteins. We have previously shown differential messenger RNA...
6.
Celli J, Rappold G, Niesler B
Hum Mutat . 2016 Oct; 38(2):137-147. PMID: 27763704
Serotonin type 3 (5-HT ) receptors are ligand-gated ion channels formed by five subunits (5-HT3A-E), which are encoded by the HTR3A, HTR3B, HTR3C, HTR3D, and HTR3E genes. Functional receptors are...
7.
Ek W, Reznichenko A, Ripke S, Niesler B, Zucchelli M, Rivera N, et al.
Gut . 2014 Sep; 64(11):1774-82. PMID: 25248455
Objective: IBS shows genetic predisposition, but adequately powered gene-hunting efforts have been scarce so far. We sought to identify true IBS genetic risk factors by means of genome-wide association (GWA)...
8.
Schroeder C, Ekici A, Moog U, Grasshoff U, Mau-Holzmann U, Sturm M, et al.
Eur J Hum Genet . 2014 May; 22(10):1233-5. PMID: 24801762
Uniparental disomy (UPD) describes the inheritance of a pair of chromosomes from only one parent. It may occur as isodisomy, heterodisomy or a combination of both and may involve only...
9.
Hammer C, Degenhardt F, Priebe L, Stutz A, Heilmann S, Waszak S, et al.
Bipolar Disord . 2014 Apr; 16(7):764-8. PMID: 24754353
Objectives: Copy number variants (CNVs) have been shown to affect susceptibility for neuropsychiatric disorders. To date, studies implicating the serotonergic system in complex conditions have just focused on single nucleotide...
10.
Blum W, Ross J, Zimmermann A, Quigley C, Child C, Kalifa G, et al.
J Clin Endocrinol Metab . 2013 May; 98(8):E1383-92. PMID: 23720786
Context: Growth impairment in short stature homeobox-containing gene (SHOX) deficiency and Turner syndrome share a similar etiology. Because of the established effect of GH treatment on height in patients with...