Wichtige Publikationen der letzten Jahre

Humangenetik

Direktor:
Prof. Dr. med. André Reis

Ausgewählte Publikationen

  • Lukassen S, Bosch E, Ekici AB, Winterpacht A (2018). Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing.
    Sci Rep. 8:6521. MEDLINE
  • Chung HR, Xu C, Fuchs A, Mund A, Lange M, Staege H, Schubert T, Bian C, Dunkel I, Eberharter A, Regnard C, Klinker H, Meierhofer D, Cozzuto L, Winterpacht A, DiCroce L, Min J, Will H, Kinkley S (2016). PHF13 is a molecular reader and transcriptional co-regulator of H3K4me2/3.
    Elife pii: e10607. MEDLINE
  • Eberhardt M, Nakajima J, Klinger AB, Neacsu C, Hühne K, O'Reilly AO, Kist AM, Lampe AK, Fischer K, Gibson J, Nau C, Winterpacht A, Lampert A. Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation (2014).
    J Biol Chem 289:1971-1980. MEDLINE
  • Grosch M, Grüner B, Spranger S, Stütz AM, Rausch T, Korbel JO, Seelow D,Nürnberg P, Sticht H, Lausch E, Zabel B, Winterpacht A, Tagariello A. Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotype (2013).
    Matrix Biol 32:387-392. MEDLINE
  • Jeschke J, Van Neste L, Glockner SC, Dhir M, Calmon MF, Deregowski V, Van Criekinge W, Vlassenbroeck I, Koch A, Chan TA, Cope L, Hooker CM, Schuebel KE, Gabrielson E, Winterpacht A, Baylin SB, Herman JG, Ahuja N (2012). Biomarkers for detection and prognosis of breast cancer identified by a functional hypermethylome screen.
    Epigenetics 7:701-709. MEDLINE
  • Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Ruffer A, Dittrich S, Schneider H, Winterpacht A, Sticht H, Dotsch J, Toka O (2012). Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta.
    Curr Mol Med 12:199-205. MEDLINE
  • Bordlein A, Scherthan H, Nelkenbrecher C, Molter T, Bosl MR, Dippold C, Birke K, Kinkley S, Staege H, Will H, Winterpacht A (2011). SPOC1 (PHF13) is required for spermatogonial stem cell differentiation and sustained spermatogenesis.
    J Cell Sci 124:3137-3148. MEDLINE
  • Neacsu CD, Grosch M, Tejada M, Winterpacht A, Paulsson M, Wagener R, Tagariello A (2011). Ucmaa (Grp-2) is required for zebrafish skeletal development. Evidence for a functional role of its glutamate gamma-carboxylation.
    Matrix Biol 30:369-378. MEDLINE
  • Endele S, Nelkenbrecher C, Bordlein A, Schlickum S, Winterpacht A (2011). C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development.
    Neurogenetics 12:155-163. MEDLINE
  • Kinkley S, Staege H, Mohrmann G, Rohaly G, Schaub T, Kremmer E, Winterpacht A, Will H (2009). SPOC1: a novel PHD-containing protein modulating chromatin structure and mitotic chromosome condensation.
    J Cell Sci 122:2946-2956. MEDLINE
 
 
 
 
 
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