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/vufind/Search/Results?lookfor=%22Welte%2C+Karl%22&type=Person&sort=year
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PubPharm (328)
1
CRISPR/Cas9n-mediated ELANE promoter editing for gene therapy of severe congenital neutropenia
enthalten in:
Molecular therapy : the journal of the American Society of Gene Therapy
| 2024
von
Nasri, M.
|
Ritter, M.
|
Mir, P.
| +11
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2
Tuning of granulopoietic signaling by
de novo
designed agonists
enthalten in:
bioRxiv.org
| 2023
von
Ullrich, T.
|
Pollmann, C.
|
Ritter, M.
| +16
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3
Correction : NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
enthalten in:
Stem cell research & therapy
| 2023
von
Xu, Y.
|
Nasri, M.
|
Dannenmann, B.
| +5
ErratumFor: Stem Cell Res Ther. 2021 Feb 5;12(1):112. - PMID 33546767
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4
Correction: NAMPT/SIRT2-mediated inhibition of the p53-p21 signaling pathway is indispensable for maintenance and hematopoietic differentiation of human iPS cells
enthalten in:
Stem cell research & therapy
| 2023
von
Xu, Y.
|
Nasri, M.
|
Dannenmann, B.
| +5
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5
Differential transcriptional control of hematopoiesis in congenital and cyclic neutropenia patients harboring ELANE mutations
enthalten in:
Haematologica
| 2023
von
Zeidler, A.
|
Borbaran-Bravo, N.
|
Dannenmann, B.
| +9
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6
iPSC modeling of stage-specific leukemogenesis reveals BAALC as a key oncogene in severe congenital neutropenia
enthalten in:
Cell stem cell
| 2023
von
Dannenmann, B.
|
Klimiankou, M.
|
Oswald, B.
| +21
ErratumFor: Cell Stem Cell. 2021 May 6;28(5):906-922.e6. - PMID 33894142
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7
HAX1-related congenital neutropenia : Long-term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry (SCNIR)
enthalten in:
British journal of haematology
| 2023
von
Pogozhykh, D.
|
Yilmaz Karapinar, D.
|
Klimiankou, M.
| +11
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8
The European Guidelines on Diagnosis and Management of Neutropenia in Adults and Children : A Consensus Between the European Hematology Association and the EuNet-INNOCHRON COST Action
enthalten in:
HemaSphere
| 2023
von
Fioredda, F.
|
Skokowa, J.
|
Tamary, H.
| +14
ErratumIn: Hemasphere. 2023 Apr 27;7(5):e897. - PMID 37125258
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9
HAX1‐related congenital neutropenia : Long‐term observation in paediatric and adult patients enrolled in the European branch of the Severe Chronic Neutropenia International Registry ( SCNIR)
enthalten in:
British Journal of Haematology
| 2023
von
Pogozhykh, D.
|
Yilmaz Karapinar, D.
|
Klimiankou, M.
| +11
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10
Corrigendum to 'Human iPSC-based model of severe congenital neutropenia reveals elevated UPR and DNA damage in CD34+ cells preceding leukemic transformation' <[Experimental Hematology, Volume 71, 2019;71:51-60]>
enthalten in:
Experimental hematology
| 2022
von
Dannenmann, B.
|
Zahabi, A.
|
Mir, P.
| +11
ErratumFor: Exp Hematol. 2019 Mar;71:51-60. - PMID 30615903
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33
Granulocyte Colony-Stimulating Factor
32
143011-72-7
19
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15
Adaptor Proteins, Signal Transducing
15
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14
HAX1 protein, human
13
RNA, Messenger
12
Multicenter Study
11
CSF3R protein, human
11
EC 3.4.21.37
11
Leukocyte Elastase
11
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10
Receptors, Granulocyte Colony-Stimulating Factor
9
Childhood
9
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9
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9
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9
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