Results 211 to 220 of about 221,346 (354)

Immune composition of the mononuclear cell fraction of human umbilical cord blood. [PDF]

open access: yesFront Immunol
Kikuta K   +7 more
europepmc   +1 more source

Post‐Transplant Cyclophosphamide for Graft‐Versus‐Host Disease Prophylaxis in Pediatric Stem Cell Transplantation

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Graft‐Versus‐Host disease (GVHD) is a leading contributor to morbidity and mortality following stem cell transplantation (SCT). Current GVHD prevention methods utilize a combination of immunosuppressive drugs to prevent injury to host tissues.
Aaron E. Fan   +6 more
wiley   +1 more source

Phenotype disruption of umbilical cord derived MSC by cyclic mechanical stretch and hyperoxia mediated by p21. [PDF]

open access: yesSci Rep
Goetz MJ   +7 more
europepmc   +1 more source

Ethnical Differences of Umbilical Cord Blood Lipoproteins

open access: bronze, 1979
Toshitaka TAMAI   +6 more
openalex   +2 more sources

Abatacept Prevents Severe Acute Graft‐Versus‐Host Disease Without Increasing Graft Failure Risk in Pediatric Bone Marrow Failure Syndromes

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Pediatric patients with inherited or acquired bone marrow failure syndromes (BMFS) often require an allogeneic hematopoietic stem cell transplant (HSCT) to cure the hematological manifestations. Amongst these, those without a matched sibling donor (MSD), are at increased risk for graft failure and are known to tolerate graft‐versus ...
Zahra Hudda   +7 more
wiley   +1 more source

Detection of neuroglobin in umbilical cord blood signals progress in perinatal medicine. [PDF]

open access: yesSci Rep
Filonzi L   +11 more
europepmc   +1 more source

Concentrations of Lipids and Apolipoprotein B in Plasma and Lipoprotein Density Classes from Japanese Umbilical Cord Blood

open access: bronze, 1979
Toshitaka TAMAI   +6 more
openalex   +2 more sources

Genetic Diagnosis and Clinical Features of Fetuses With Congenital Diaphragmatic Hernia

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective Congenital diaphragmatic hernia (CDH) is a rare abnormality with highly heterogeneous genetic causes. This study investigated chromosomal and monogenic abnormalities in fetal CDH patients and evaluated the efficacy of chromosomal microarray analysis (CMA) and whole‐exome sequencing (WES) for genetic diagnosis.
Yan Lü   +18 more
wiley   +1 more source

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