Andreas Kispert


Ontology type: schema:Person     


Person Info

NAME

Andreas

SURNAME

Kispert

Publications in SciGraph latest 50 shown

  • 2017-12 Retinoic acid signaling maintains epithelial and mesenchymal progenitors in the developing mouse ureter in SCIENTIFIC REPORTS
  • 2016-06 Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics in NAUNYN-SCHMIEDEBERG'S ARCHIVES OF PHARMACOLOGY
  • 2016-04 GTPase domain driven dimerization of SEPT7 is dispensable for the critical role of septins in fibroblast cytokinesis in SCIENTIFIC REPORTS
  • 2016-03 Eph/ephrin signaling in the kidney and lower urinary tract in PEDIATRIC NEPHROLOGY
  • 2016-01 Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT) in HUMAN GENETICS
  • 2015-12 Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism in NATURE COMMUNICATIONS
  • 2012-12 The transcription factor Uncx4.1 acts in a short window of midbrain dopaminergic neuron differentiation in NEURAL DEVELOPMENT
  • 2012-04 Tbx2 and Tbx3 induce atrioventricular myocardial development and endocardial cushion formation in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2012-03 Comparative analysis of Neph gene expression in mouse and chicken development in HISTOCHEMISTRY AND CELL BIOLOGY
  • 2011-01 CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs in NATURE GENETICS
  • 2010-02 AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis in NATURE GENETICS
  • 2009-04-16 Tbx18 and the fate of epicardial progenitors in NATURE
  • 2009-01 Secreted Frizzled-related protein 2 is a procollagen C proteinase enhancer with a role in fibrosis associated with myocardial infarction in NATURE CELL BIOLOGY
  • 2007-12 Down the tube of obstructive nephropathies: The importance of tissue interactions during ureter development in KIDNEY INTERNATIONAL
  • 2005-03 Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin in NATURE GENETICS
  • 2004-08 Analysis of TBX18 expression in chick embryos in DEVELOPMENT GENES AND EVOLUTION
  • 2003-08 Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in NATURE GENETICS
  • 2003-08 Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination in NATURE GENETICS
  • 2002-02 Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry in NATURE GENETICS
  • 2001-11 Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure in NATURE GENETICS
  • 1999-11 A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance in NATURE
  • 1999-08 The mouse Rsk3 gene maps to the Leh66 elements carrying the t-complex responder Tcr in MAMMALIAN GENOME
  • 1999-02 Female development in mammals is regulated by Wnt-4 signalling in NATURE
  • 1997-11 A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column, kidney and nervous system in DEVELOPMENT GENES AND EVOLUTION
  • 1995-10 Promotion of gastrulation by maternal growth factor in cultured rabbit blastocysts in CELL AND TISSUE RESEARCH
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