Publications by authors named "Georg Bohn"

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High resolution IgH repertoire analysis reveals fetal liver as the likely origin of life-long, innate B lymphopoiesis in humans.
Anindita Roy, Vojtech Bystry, Georg Bohn, Katerina Goudevenou, Tomas Reigl

Clin Immunol· October 2017

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Nuclear proteasomes carry a constitutive posttranslational modification which derails SDS-PAGE (but not CTAB-PAGE).
David S Pitcher, Kate de Mattos-Shipley, Ziming Wang, Konstantinos Tzortzis, Katerina Goudevenou, Georg Bohn

Biochim Biophys Acta· December 2014

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A complex immunodeficiency is based on U1 snRNP-mediated poly(A) site suppression.
Jörg Langemeier, Eva-Maria Schrom, Alona Rabner, Maximilian Radtke, Daniela Zychlinski, Georg Bohn, Jens Bohne

EMBO J· October 2012

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Perturbation of fetal liver hematopoietic stem and progenitor cell development by trisomy 21.
Anindita Roy, Gillian Cowan, Adam J Mead, Sarah Filippi, Georg Bohn

Proc Natl Acad Sci U S A· October 2012

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Lethal graft-versus-host disease in congenital neutropenia caused by p14 deficiency after allogeneic bone marrow transplantation from an HLA-identical sibling.
Georg Bohn, Matthias Hardtke-Wolenski, Cornelia Zeidler, Britta Maecker, Martin Sauer

Pediatr Blood Cancer· September 2008

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Severe congenital neutropenia: new genes explain an old disease.
Georg Bohn, Karl Welte, Christoph Klein

Curr Opin Rheumatol· November 2007

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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
Christoph Klein, Magda Grudzien, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Georg Bohn

Nat Genet· January 2007

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A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14.
Georg Bohn, Anna Allroth, Gudrun Brandes, Jens Thiel, Erik Glocker

Nat Med· January 2007

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p14-MP1-MEK1 signaling regulates endosomal traffic and cellular proliferation during tissue homeostasis.
David Teis, Nicole Taub, Robert Kurzbauer, Diana Hilber, Mariana E de Araujo, Georg Bohn

J Cell Biol· December 2006

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Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2.
Johannes Jung, Georg Bohn, Anna Allroth, Kaan Boztug, Gudrun Brandes

Blood· July 2006

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Clinically silent infection in a premature infant.
Georg Bohn, Odell Wilson, Flor M Munoz

Semin Pediatr Infect Dis· April 2004

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