Ulrich Pannicke: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Mechanism and regulation of human non-homologous DNA end-joining

Lieber, Michael R., Ma, Yunmei, Pannicke, Ulrich, Schwarz, Klaus

Journal:

Nature Reviews Molecular Cell Biology

Year:

2003

Language:

english

File:

PDF, 391 KB

english, 2003

2

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

Åyszkiewicz, Marcin, ZiÄtara, Natalia, Frey, Laura, Pannicke, Ulrich, Stern, Marcel, Liu, Yanshan, Fan, Yanxin, PuchaÅka, Jacek, Hollizeck, Sebastian, Somekh, Ido, Rohlfs, Meino, Yilmaz, TuÄba, Ã

Journal:

Nature Communications

Year:

2020

Language:

english

File:

PDF, 3.81 MB

english, 2020

3

Retroviral WASP gene transfer into human hematopoietic stem cells reconstitutes the actin cytoskeleton in myeloid progeny cells differentiated in vitro

Ricardo A. Dewey, Inés Avedillo Díez, Matthias Ballmaier, Alexandra Filipovich, Johann Greil, Tayfun Güngör, Christoph Happel, Alexey Maschan, Fatih Noyan, Ulrich Pannicke, Klaus Schwarz, Scott Snappe

Journal:

Experimental Hematology

Year:

2006

Language:

english

File:

PDF, 430 KB

english, 2006

4

Targeted Therapy with Eculizumab for Inherited CD59 Deficiency

Höchsmann, Britta, Dohna-Schwake, Christian, Kyrieleis, Henriette A., Pannicke, Ulrich, Schrezenmeier, Hubert

Journal:

New England Journal of Medicine

Year:

2014

Language:

english

File:

PDF, 394 KB

english, 2014

5

Regulated Expression of Nuclear Receptor RORγt Confers Distinct Functional Fates to NK Cell Receptor-Expressing RORγt+ Innate Lymphocytes

Cedric Vonarbourg, Arthur Mortha, Viet L. Bui, Pedro P. Hernandez, Elina A. Kiss, Thomas Hoyler, Melanie Flach, Bertram Bengsch, Robert Thimme, Christoph Hölscher, Manfred Hönig, Ulrich Pannicke, Klau

Journal:

Year:

2010

Language:

english

File:

PDF, 2.15 MB

english, 2010

6

Late thymic deficiency after HLA-haploidentical hematopoietic stem cell transplantation for severe combined immunodeficiency

Ege, Markus J., Schuetz, Catharina, Jacobsen, Eva-Maria, Müller-Langer, Susanna M., Furlan, Ingrid, Sirin, Mehtap, Pannicke, Ulrich, Schwarz, Klaus, Debatin, Klaus-Michael, Hönig, Manfred, Schulz, Ans

Journal:

Journal of Allergy and Clinical Immunology

Year:

2018

Language:

english

File:

PDF, 1.07 MB

english, 2018

7

Functional and biochemical dissection of the structure-specific nuclease ARTEMIS

Pannicke, Ulrich, Ma, Yunmei, Hopfner, Karl-Peter, Niewolik, Doris, Lieber, Michael R, Schwarz, Klaus

Journal:

The EMBO Journal

Year:

2004

Language:

english

File:

PDF, 309 KB

english, 2004

8

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Volk, Timo, Pannicke, Ulrich, Reisli, Ismail, Bulashevska, Alla, Ritter, Julia, Björkman, Andrea, Schäffer, Alejandro A., Fliegauf, Manfred, Sayar, Esra H., Salzer, Ulrich, Fisch, Paul, Pfeifer, Dietm

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 833 KB

english, 2015

9

Recent advances in understanding the pathogenesis and management of reticular dysgenesis

Hoenig, Manfred, Pannicke, Ulrich, Gaspar, Hubert B., Schwarz, Klaus

Journal:

British Journal of Haematology

Year:

2017

Language:

english

File:

PDF, 375 KB

english, 2017

10

The mechanism of vertebrate nonhomologous DNA end joining and its role in V(D)J recombination

Michael R Lieber, Yunmei Ma, Ulrich Pannicke, Klaus Schwarz

Journal:

Year:

2004

Language:

english

File:

PDF, 358 KB

english, 2004

11

Macrophages of patients with X-linked thrombocytopenia display an attenuated Wiskott-Aldrich syndrome phenotype

Linder, Stefan, Wintergerst, Uwe, Bender-Gotze, Christine, Schwarz, Klaus, Pannicke, Ulrich, Aepfelbacher, Martin

Journal:

Immunology & Cell Biology

Year:

2003

Language:

english

File:

PDF, 814 KB

english, 2003

12

Dihydrofolate Reductase Deficiency Due to a Homozygous DHFR Mutation Causes Megaloblastic Anemia and Cerebral Folate Deficiency Leading to Severe Neurologic Disease

Holger Cario, Desirée E.C. Smith, Henk Blom, Nenad Blau, Harald Bode, Karlheinz Holzmann, Ulrich Pannicke, Karl-Peter Hopfner, Eva-Maria Rump, Zuleya Ayric, Elisabeth Kohne, Klaus-Michael Debatin, Yvo

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 382 KB

english, 2011

13

Chronic Inflammatory Bowel Disease as Key Manifestation of Atypical ARTEMIS Deficiency

Jan Rohr, Ulrich Pannicke, Michaela Döring, Annette Schmitt-Graeff, Elisabeth Wiech, Andreas Busch, Carsten Speckmann, Ingo Müller, Peter Lang, Rupert Handgretinger, Paul Fisch, Klaus Schwarz, Stephan

Journal:

Journal of Clinical Immunology

Year:

2010

Language:

english

File:

PDF, 325 KB

english, 2010

14

Two siblings with lethal pneumococcal meningitis in a family with a mutation in Interleukin-1 receptor–associated kinase 4

Anselm Enders, Ulrich Pannicke, Reinhard Berner, Phillip Henneke, Klaus Radlinger, Klaus Schwarz, Stephan Ehl

Journal:

The Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 86 KB

english, 2004

15

Disulfide Bridge Disruption in the α2 Domain of the HLA Class I Molecule Leads to Low Expression of the Corresponding Antigen

Kaimo Hirv, Ulrich Pannicke, Joannis Mytilineos, Klaus Schwarz

Journal:

Human Immunology

Year:

2006

Language:

english

File:

PDF, 250 KB

english, 2006

16

Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in THPO

Seo, Aaron, Ben-Harosh, Miri, Sirin, Mehtap, Stein, Jerry, Dgany, Orly, Kaplelushnik, Joseph, Hoenig, Manfred, Pannicke, Ulrich, Lorenz, Myriam, Schwarz, Klaus, Stockklausner, Clemens, Walsh, Tom, Gul

Journal:

Year:

2017

Language:

english

File:

PDF, 883 KB

english, 2017

17

Human severe combined immune deficiency and DNA repair

Klaus Schwarz, Yunmei Ma, Ulrich Pannicke, Michael R. Lieber

Journal:

Year:

2003

Language:

english

File:

PDF, 212 KB

english, 2003

18

Deficiency of Innate and Acquired Immunity Caused by an IKBKB Mutation

Pannicke, Ulrich, Baumann, Bernd, Fuchs, Sebastian, Henneke, Philipp, Rensing-Ehl, Anne, Rizzi, Marta, Janda, Ales, Hese, Katrin, Schlesier, Michael, Holzmann, Karlheinz, Borte, Stephan, Laux, Constan

Journal:

New England Journal of Medicine

Year:

2013

Language:

english

File:

PDF, 808 KB

english, 2013

19

Reticular dysgenesis: international survey on clinical presentation, transplantation and outcome

Hoenig, Manfred, Lagresle-Peyrou, Chantal, Pannicke, Ulrich, Notarangelo, Luigi D., Porta, Fulvio, Gennery, Andrew R., Slatter, Mary, Cowan, Morton J., Stepensky, Polina, Al-Mousa, Hamoud, Al-Zahrani,

Journal:

Year:

2017

Language:

english

File:

PDF, 530 KB

english, 2017

20

Transplantation from a symptomatic carrier sister restores host defenses but does not prevent colitis in NEMO deficiency

Klemann, Christian, Pannicke, Ulrich, Morris-Rosendahl, Deborah J., Vlantis, Katerina, Rizzi, Marta, Uhlig, Holm, Vraetz, Thomas, Speckmann, Carsten, Strahm, Brigitte, Pasparakis, Manolis, Schwarz, Kl

Journal:

Clinical Immunology

Year:

2016

Language:

english

File:

PDF, 522 KB

english, 2016

21

Hairpin Opening and Overhang Processing by an Artemis/DNA-Dependent Protein Kinase Complex in Nonhomologous End Joining and V(D)J Recombination

Yunmei Ma, Ulrich Pannicke, Klaus Schwarz, Michael R. Lieber

Journal:

Year:

2002

Language:

english

File:

PDF, 411 KB

english, 2002

22

An Immunodeficiency Disease with RAG Mutations and Granulomas

Schuetz, Catharina, Huck, Kirsten, Gudowius, Sonja, Megahed, Mosaad, Feyen, Oliver, Hubner, Bernd, Schneider, Dominik T., Manfras, Burkhard, Pannicke, Ulrich, Willemze, Rein, Knüchel, Ruth, Göbel, Ulr

Journal:

Boston Medical and Surgical Journal

Year:

2008

Language:

english

File:

PDF, 442 KB

english, 2008

23

Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2

Pannicke, Ulrich, Hönig, Manfred, Hess, Isabell, Friesen, Claudia, Holzmann, Karlheinz, Rump, Eva-Maria, Barth, Thomas F, Rojewski, Markus T, Schulz, Ansgar, Boehm, Thomas

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 537 KB

english, 2008

24

Evaluation of RAG1 mutations in an adult with combined immunodeficiency and progressive multifocal leukoencephalopathy

Schröder, Claudia, Baerlecken, Niklas Thomas, Pannicke, Ulrich, Dörk, Thilo, Witte, Torsten, Jacobs, Roland, Stoll, Matthias, Schwarz, Klaus, Grimbacher, Bodo, Schmidt, Reinhold E., Atschekzei, Farana

Journal:

Clinical Immunology

Year:

2017

Language:

english

File:

PDF, 1.05 MB

english, 2017

25

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

Åyszkiewicz, Marcin, ZiÄtara, Natalia, Frey, Laura, Pannicke, Ulrich, Stern, Marcel, Liu, Yanshan, Fan, Yanxin, PuchaÅka, Jacek, Hollizeck, Sebastian, Somekh, Ido, Rohlfs, Meino, Yilmaz, TuÄba, Ã

Journal:

Nature Communications

Year:

2020

File:

PDF, 437 KB

2020

26

The most frequent DCLRE1C (ARTEMIS) mutations are based on homologous recombination events

Ulrich Pannicke, Manfred Hönig, Ilka Schulze, Jan Rohr, Gitta A. Heinz, Sylvia Braun, Ingrid Janz, Eva-Maria Rump, Markus G. Seidel, Susanne Matthes-Martin, Jan Soerensen, Johann Greil, Daniel K. Stac

Journal:

Year:

2010

Language:

english

File:

PDF, 293 KB

english, 2010

27

Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be tested

Schuetz, Catharina, Pannicke, Ulrich, Jacobsen, Eva-Maria, Burggraf, Siegfried, Albert, Michael H., Hönig, Manfred, Niehues, Tim, Feyen, Oliver, Ehl, Stephan, Debatin, Klaus-Michael, Friedrich, Wilhel

Journal:

Journal of Allergy and Clinical Immunology

Year:

2014

Language:

english

File:

PDF, 402 KB

english, 2014

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски