Publications by authors named "Anja Brehm"

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Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype.
Bertrand Isidor, Frédéric Ebstein, Anna Hurst, Marie Vincent, Ingrid Bader, Anja Brehm

Genet Med· January 2022

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Glyco-engineered HEK 293-F cell lines for the production of therapeutic glycoproteins with human N-glycosylation and improved pharmacokinetics.
Rico Uhler, Ruth Popa-Wagner, Mario Kröning, Anja Brehm, Paul Rennert

Glycobiology· August 2021

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Molecular coevolution of coagulation factor VIII and von Willebrand factor.
Philip M Zakas, Christopher W Coyle, Anja Brehm, Marion Bayer, Barbara Solecka-Witulska

Blood Adv· February 2021

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Novel proteasome assembly chaperone mutations in PSMG2/PAC2 cause the autoinflammatory interferonopathy CANDLE/PRAAS4.
Adriana A de Jesus, Anja Brehm, Rachel VanTries, Pascal Pillet, Anne-Sophie Parentelli

J Allergy Clin Immunol· May 2019

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TCF11/Nrf1-Mediated Induction of Proteasome Expression Prevents Cytotoxicity by Rotenone.
Franziska Sotzny, Eileen Schormann, Ina Kühlewindt, Annett Koch, Anja Brehm

Antioxid Redox Signal· December 2016

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Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
Anja Brehm, Yin Liu, Afzal Sheikh, Bernadette Marrero, Ebun Omoyinmi

J Clin Invest· February 2016

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Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production.
Anja Brehm, Yin Liu, Afzal Sheikh, Bernadette Marrero, Ebun Omoyinmi

J Clin Invest· November 2015

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Dysfunction in protein clearance by the proteasome: impact on autoinflammatory diseases.
Anja Brehm, Elke Krüger

Semin Immunopathol· July 2015

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Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.
Eva Klopocki, Silke Lohan, Francesco Brancati, Randi Koll, Anja Brehm

Am J Hum Genet· January 2011

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Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN.
Petra Seemann, Anja Brehm, Jana König, Carsten Reissner, Sigmar Stricker

PLoS Genet· November 2009

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Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2.
Katarina Dathe, Klaus W Kjaer, Anja Brehm, Peter Meinecke, Peter Nürnberg

Am J Hum Genet· April 2009

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