about
Patients with rare diseases: from therapeutic orphans to pioneers of personalized treatments.Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.Front-line imatinib treatment in children and adolescents with chronic myeloid leukemia: results from a phase III trialProteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent AcquisitionHuman FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cellsComprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemiaLeukemia-induced dysfunctional TIM-3+CD4+ bone marrow T cells increase risk of relapse in pediatric B-precursor ALL patientsAuthor Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells
P50
Q48228930-1B8BB2D0-810C-4A21-89E4-C47C765DB575Q52372466-955DB5F3-1DE9-4918-A501-CD6071484BE8Q56967295-4BA8B368-19C1-4731-8F0E-74CECF7C7EF2Q64041481-00FFC03D-D476-4254-8CD7-37F7B3066BFDQ89882216-66A07BB2-B360-4EA9-ABD2-B34C50734769Q90010381-C2C08F65-4172-4212-BDCE-D7161F69CBEDQ90589512-C5A0C826-783A-4DE4-B57D-05E63EAD7630Q92092783-08FEC1A9-15FD-41BE-95BB-68B98C730830
P50
description
researcher
@en
wetenschapper
@nl
name
Christoph Klein
@en
Christoph Klein
@nl
type
label
Christoph Klein
@en
Christoph Klein
@nl
prefLabel
Christoph Klein
@en
Christoph Klein
@nl
P31
P496
0000-0003-0956-0445