Results 281 to 290 of about 1,719,427 (359)

Long‐term demography and spatial genetic structure reveal mechanisms of Sassafras albidum population persistence through clonality

open access: yesAmerican Journal of Botany, EarlyView.
Abstract Premise Vegetative regeneration is a key mechanism of woody plant persistence in forest ecosystems, and the coupled roles of basal sprouting and clonal growth in shaping long‐term population dynamics have been understudied. Basal sprouting replaces stems at fixed ramet locations, whereas clonal growth via root suckering produces spatially ...
J. T. Michel   +3 more
wiley   +1 more source

Multiplex PCR-based rapid pathogen identification in acute cholecystitis using the FilmArray BCID2 panel. [PDF]

open access: yesFront Microbiol
Nakamura G   +10 more
europepmc   +1 more source

Post CAR‐T Measurable Residual Disease Monitoring in Mantle Cell Lymphoma Enables Early Detection of Disease Relapse

open access: yesAmerican Journal of Hematology, EarlyView.
ABSTRACT CD19‐directed chimeric antigen receptor (CAR) T‐cell therapy has transformed outcomes for patients with relapsed or refractory (r/r) mantle cell lymphoma (MCL), yet more than 40% relapse within one year. Early identification of patients at risk for progression could inform post CAR‐T surveillance and consolidation strategies.
Snegha Ananth   +12 more
wiley   +1 more source

Multicenter evaluation of fast multiplex PCR for detection of pathogens in lower respiratory tract infections. [PDF]

open access: yesFront Cell Infect Microbiol
Wang L   +14 more
europepmc   +1 more source

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle   +10 more
wiley   +1 more source

A Novel Splice Variant in ERGIC1 Causes Arthrogryposis Multiplex Congenita—Characterization Using Urine‐Derived Cells

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is defined as the presence of joint contractures affecting at least two body regions at birth. Three different ERGIC1 variants have been reported in individuals with AMC. Here, we report on a 16‐year‐old male with a homozygous ERGIC1 c.250+1G>A variant that was classified as a variant of uncertain ...
Lauren Kerr   +7 more
wiley   +1 more source

A Modified Method Incorporating Multiplex PCR Reveals Fusobacterium Prevalence in Southern Chinese Population and Its Correlations in Cancers. [PDF]

open access: yesMicrob Biotechnol
Shen T   +19 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy