International registry: genetic and phenotypic characteristics of a heterogenous group of disorders

por Zeidler, Cornelia, Pracht, Gusal, Germeshausen, Manuela, Welte, Karl
Publicado 2010

Tumor necrosis factor and lymphotoxin-alpha genetic polymorphisms and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia: a case-control study of patients t...

por Stanulla, Martin, Schrauder, André, Welte, Karl, Schrappe, Martin
Publicado 2001

P458: HIPSC DISEASE MODELING TO STUDY LEUKEMIA DEVELOPMENT IN HAX1 VS ELANE ASSOCIATED CONGENITAL NEUTROPENIA

por Dannenmann, Benjamin, Klimiankou, Maksim, Zeidler, Cornelia, Welte, Karl, Skokowa, Julia
Publicado 2023

A zebrafish model for HAX1-associated congenital neutropenia

por Doll, Larissa, Aghaallaei, Narges, Dick, Advaita M., Welte, Karl, Skokowa, Julia, Bajoghli, Baubak
Publicado 2020

Rolf Neth (October 6, 1926 to March 17, 2020)

por Hehlmann, Rüdiger, Gallo, Robert, Hoelzer, Dieter, Welte, Karl, Gale, Robert Peter, Zander, Axel
Publicado 2020

Publisher Correction: Rolf Neth (October 6, 1926–March 17, 2020)

por Hehlmann, Rüdiger, Gallo, Robert, Hoelzer, Dieter, Welte, Karl, Gale, Robert Peter, Zander, Axel
Publicado 2021

P750: A ZEBRAFISH MODEL FOR JAGN1-ASSOCIATED SEVERE CONGENITAL NEUTROPENIA

por Doll, Larissa, Aghaallaei, Narges, Lengerke, Claudia, Zeidler, Cornelia, Welte, Karl, Skokowa, Julia, Bajoghli, Baubak
Publicado 2023

Human Endothelial Cells Regulate Survival and Proliferation of Human Mast Cells

por Mierke, Claudia T., Ballmaier, Matthias, Werner, Uwe, Manns, Michael P., Welte, Karl, Bischoff, Stephan C.
Publicado 2000

Genetic polymorphisms of the lymphotoxin alpha gene are associated with increased risk for lethal infections during induction therapy for childhood acute leukemia: a case-control s...

por Kidas, Ekaterini, Möricke, Anja, Beier, Rita, Welte, Karl, Schrappe, Martin, Stanulla, Martin, Grigull, Lorenz
Publicado 2009

Correction: NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells

por Xu, Yun, Nasri, Masoud, Dannenmann, Benjamin, Mir, Perihan, Zahabi, Azadeh, Welte, Karl, Morishima, Tatsuya, Skokowa, Julia
Publicado 2023

NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells

por Xu, Yun, Nasri, Masoud, Dannenmann, Benjamin, Mir, Perihan, Zahabi, Azadeh, Welte, Karl, Morishima, Tatsuya, Skokowa, Julia
Publicado 2021

P780: G-CSF THERAPY IN EUROPEAN PATIENTS WITH SHWACHMAN-DIAMOND SYNDROME

por Mellor-Heineke, Sabine, Skokowa, Julia, Gerschmann, Natali, Deordieva, Ekatharina, Schsherbina, Anna, Tesakov, Ivan, Welte, Karl, Zeidler, Cornelia
Publicado 2023

Involvement of p53 in the cytotoxic activity of the NAMPT inhibitor FK866 in myeloid leukemic cells

por Thakur, Basant Kumar, Dittrich, Tino, Chandra, Prakash, Becker, Annette, Kuehnau, Wolfgang, Klusmann, Jan-Henning, Reinhardt, Dirk, Welte, Karl
Publicado 2013

Ultra-Sensitive CSF3R Deep Sequencing in Patients With Severe Congenital Neutropenia

por Klimiankou, Maksim, Uenalan, Murat, Kandabarau, Siarhei, Nustede, Rainer, Steiert, Ingeborg, Mellor-Heineke, Sabine, Zeidler, Cornelia, Skokowa, Julia, Welte, Karl
Publicado 2019

Cooperating, congenital neutropenia–associated Csf3r and Runx1 mutations activate pro-inflammatory signaling and inhibit myeloid differentiation of mouse HSPCs

por Ritter, Malte, Klimiankou, Maksim, Klimenkova, Olga, Schambach, Axel, Hoffmann, Dirk, Schmidt, Amy, Kanz, Lothar, Link, Daniel C., Welte, Karl, Skokowa, Julia
Publicado 2020

P751: UNRAVELING THE DIFFERENT PATHOMECHANISMS OF CONGENITAL AND CYCLIC NEUTROPENIAS: CYCLIC EXPRESSION OF HEMATOPOIETIC STEM-CELL-SPECIFIC TRANSCRIPTION FACTORS IN CYCLIC NEUTROPE...

por Alexander Zeidler, Karl, Borbaran-Bravo, Natalia, Ritter, Malte, Nasri, Masoud, Klimiankou, Maksim, Kandabarau, Sergey, König, Josef, Zeidler, Cornelia, Skokowa, Julia, Welte, Karl
Publicado 2023

Polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and susceptibility to pediatric acute lymphoblastic leukemia in a German study population

por Schnakenberg, Eckart, Mehles, Andrea, Cario, Gunnar, Rehe, Klaus, Seidemann, Kathrin, Schlegelberger, Brigitte, Elsner, Holger A, Welte, Karl H, Schrappe, Martin, Stanulla, Martin
Publicado 2005

G-CSF mobilised granulocyte transfusions in 32 paediatric patients with neutropenic sepsis

por Grigull, Lorenz, Pulver, Nicole, Goudeva, Lilia, Sykora, Karl-Walter, Linderkamp, Christin, Beilken, Andreas, Seidemann, Kathrin, Schmid, Hansjörg, Welte, Karl, Heuft, Hans-Gert
Publicado 2006

S178: A NEW HEREDITARY SYNDROME WITH SEVERE NEUTROPENIA AND NEUROLOGICAL INVOLVEMENT CAUSED BY THE AUTOSOMAL RECESSIVE COPZ1 MUTATION

por Borbaran Bravo, Natalia, Doll, Larissa, Deordieva, Ekaterina, Bräuning, Sandro, Dannenmann, Benjamin, Elgamacy, Mohammad, Zakharova, Viktoria, Lengerke, Claudia, Zeidler, Cornelia, Welte, Karl, Shcherbina, Anna, Skokowa, Julia, Klimiankou, Maksim
Publicado 2023

Design of novel granulopoietic proteins by topological rescaffolding

por Hernandez Alvarez, Birte, Skokowa, Julia, Coles, Murray, Mir, Perihan, Nasri, Masoud, Maksymenko, Kateryna, Weidmann, Laura, Rogers, Katherine W., Welte, Karl, Lupas, Andrei N., Müller, Patrick, ElGamacy, Mohammad
Publicado 2020