Results 111 to 120 of about 2,147 (210)

Die Stasi-Vergangenheit und ihre Bewältigung in der EKD

, 2013
Die Arbeit befasst sich mit der Stasi-Vergangenheit in der Evangelischen Kirche unter Pfarrern und bietet einen geschichtlichen Hintergrund über das MfS und die Friedliche Revolution, weiterhin liefert eine Fallstudie über einen aktuellen Fall aus dem ...
Farkas, Gyöngyi
core  

Episignature leads to diagnosis and reclassification of DYRK1A variant in a child with syndromic neurodevelopmental disorder: a case report. [PDF]

Front Genet
Al-Younis I, Basque L, Crapoulet N, Dyack S, Del Caño-Ochoa F, Ramón-Maiques S, MacKay SB, Rzasa J, Sadikovic B, McConkey H, Ben Amor M.   +10 more
europepmc   +1 more source

Gender differences in biochemical characteristics and health-related quality of life among hemodialysis patients. [PDF]

BMC Nephrol
Khedr L, Halim A, Emara A, Talaat B, Ali M.   +4 more
europepmc   +1 more source

Accuracy of epilepsy screening tools in community and primary care settings across countries in Sub-Saharan Africa: systematic review and meta-analysis protocol. [PDF]

BMJ Open
Darkwa EK, Cross JH, Adjei P, Newton CR, Sen A, Akpalu A, Sander JW, Danso-Appiah A.   +7 more
europepmc   +1 more source

TLR9 signaling requires ligand-induced phosphorylation of two specific tyrosine residues by EGFR and Syk. [PDF]

mBio
Veleeparambil M, Wang C, Kessler PM, Sengupta P, Das S, Chakravarti R, Willard B, Sen GC, Chattopadhyay S.   +8 more
europepmc   +1 more source

The growth hormone/IGF-1 axis is a risk factor for long-term kidney allograft failure. [PDF]

JCI Insight
Cusick M, Nair V, Fermin D, Hartman J, Beamish JA, Sun Z, Zhang Z, Otto E, Menon R, Nadimidla S, Demchuk N, Shaffer K, Heeger P, Zhang W, Menon MC, Kretzler M, Wiggins RC, Naik AS.   +17 more
europepmc   +1 more source

Ein kirchenhistorischer Zwischenruf

, 2012
Kaufmann, Thomas, Kirchenamt der EKD
core  

Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype. [PDF]

Nat Commun
Parenti I, Hesters A, Gil-Salvador M, Duffy L, Kanber D, Beygo J, Kerkhof J, Steenpaß L, Leitão E, Woestefeld J, Boone PM, Kao EM, Alabdi L, Aldhalaan HM, Alkuraya FS, Alshammari MJ, Antonarakis SE, Basel D, Cassinari K, de Polli Cellin L, Clause AR, de Lima Jorge AA, de Castro Leal A, Collins SC, Durand B, Eckhold J, Hashem MO, Jayakar P, Khan AO, Kato K, Kubica R, Lyon GJ, Marchi E, McCarrier J, Kimmig LK, Mizuno S, Nicolas G, Nishio Y, Ogi T, Pié J, Prell J, Puisac B, Ramos FJ, Ranza E, Redin C, Rush E, Saitoh S, Shamseldin HE, Starling S, Astiazaran-Symonds E, Eltahir SH, Kuechler A, Sadikovic B, Yalcin B, Wendt KS, Kaiser FJ.   +55 more
europepmc   +1 more source

EKD will Johannes-a-Lascio-Bibliothek retten

, 2009
Jürgen Plieninger
core  

SCN1A pathogenic variants do not have a distinctive blood-derived DNA methylation signature. [PDF]

Epilepsia
LaFlamme CW, Karimi K, Rastin C, Almanza Fuerte EP, Allan T, Russ-Hall SJ, Schneider AL, Stobo D, Lesca G, Symonds JD, Brunklaus A, Sadleir LG, Scheffer IE, Sadikovic B, Mefford HC.   +14 more
europepmc   +1 more source