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European Journal of Pediatrics|September 30, 2011
Liddle syndrome in a Serbian family and literature review of underlying mutationsRadovan Bogdanović, Vladimir Kuburović, Nataša Stajić, et al.
Development (Cambridge, England)|January 27, 2016
Tpbpa-Cre-mediated deletion of TFAP2C leads to deregulation of Cdkn1a, Akt1 and the ERK pathway, causing placental growth arrestNeha Sharma, Caroline Kubaczka, Stephanie Kaiser, et al.
Pediatric Surgery International|March 17, 2012
Familial occurrence of the VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Markus Draaken, et al.
Journal of Translational Medicine|May 13, 2021
Deconvolution of sarcoma methylomes reveals varying degrees of immune cell infiltrates with association to genomic aberrationsMalte Simon, Sadaf S Mughal, Peter Horak, et al.
International Journal of Molecular Medicine|September 11, 2012
Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T geneMarkus Draaken, Wiebke Prins, Claudia Zeidler, et al.
Frontiers in Immunology|March 3, 2020
Macrophages/Microglia Represent the Major Source of Indolamine 2,3-Dioxygenase Expression in Melanoma Metastases of the BrainDayana Herrera-Rios, Sadaf S Mughal, Sarah Teuber-Hanselmann, et al.
Acta Neuropathologica Communications|May 3, 2025
Identification and characterization of tertiary lymphoid structures in brain metastasesSadaf S Mughal, Yvonne Reiss, Jörg Felsberg, et al.
BMC Bioinformatics|May 30, 2019
TelomereHunter - in silico estimation of telomere content and composition from cancer genomesLars Feuerbach, Lina Sieverling, Katharina I Deeg, et al.
Oncoimmunology|April 14, 2017
PD-L1 (CD274) copy number gain, expression, and immune cell infiltration as candidate predictors for response to immune checkpoint inhibitors in soft-tissue sarcomaJan Budczies, Gunhild Mechtersheimer, Carsten Denkert, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|January 30, 2013
Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12Markus Draaken, Sadaf S Mughal, Tracie Pennimpede, et al.
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