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UnknownBimekizumab Complete Clearance of Both Skin and Nail Psoriasis: Comparative Efficacy in Phase III/IIIb Studies.
Not available
S-EPMC12615549 | biostudies-literature
UnknownMixed chimerism and acceptance of kidney transplants after immunosuppressive drug withdrawal.
Not available
S-EPMC8051148 | biostudies-literature
UnknownDe novo mutations in KIF1A cause progressive encephalopathy and brain atrophy.
Not available
S-EPMC4479523 | biostudies-literature
UnknownLong-Term Safety of Guselkumab in Patients with Psoriatic Disease: An Integrated Analysis of Eleven Phase II/III Clinical Studies in Psoriasis and Psoriatic Arthritis.
Not available
S-EPMC10764399 | biostudies-literature
UnknownCommon viruses associated with lower pediatric multiple sclerosis risk.
Not available
S-EPMC3109881 | biostudies-literature
TranscriptomicsGene Expression Test for Operational Renal Allograft Tolerance
Genomic Analysis of more than 400 patients from multi-center transplant programs and clinical trials provides a non-invasive QPCR based gene expression test for operational renal allograft tolerance 3 group comparison of blood from TOL, CAN and Non-transplant healthy controls (HD) allografts. Biolog...
ORGANISM(S): Homo sapiens 
2015-01-08 | E-GEOD-45218 | biostudies-arrayexpress
TranscriptomicsInducing and Predicting Immune Tolerance After Kidney Transplantation
Background Immune tolerance and persistent mixed chimerism can be achieved reproducibly after combined organ and hematopoietic cell transplantation in mice conditioned with total lymphoid irradiation plus anti-thymocyte globulin. We studied the safety and reproducibility of this approach in a cohort...
ORGANISM(S): Homo sapiens 
2012-12-15 | E-GEOD-17068 | biostudies-arrayexpress
UnknownTruncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature.
Not available
S-EPMC8206150 | biostudies-literature
UnknownGenetic effects on gene expression across human tissues.
Not available
S-EPMC5776756 | biostudies-literature
UnknownHeterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disability.
Not available
S-EPMC11739880 | biostudies-literature
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