Results 131 to 140 of about 103,507 (289)

Advances in research on autophagy in the maintenance of insect–microbe symbiosis

open access: yesNew Plant Protection, EarlyView.
Autophagy plays a dual regulatory role in insect–microbe symbiotic relationships. Beneficial symbiotic bacteria in insects participate in nutrient exchange via the TOR pathway, whereas pathogenic microbes induce immune defense through the AMPK pathway. Autophagy‐related genes regulate development and pathogen clearance during this process.
Yanbin Wang   +5 more
wiley   +1 more source

No way back: decadal lack of functional recovery of a coralligenous community in a warming Mediterranean

open access: yesOikos, EarlyView.
Anthropogenic disturbances are degrading nature at a rate that exceeds its capacity to recover. While considerable research has focused on understanding ecosystem impacts, recovery processes remain comparatively overlooked, particularly in marine ecosystems, where long‐term data on how highly complex systems respond to disturbances are scarce.
Yanis Zentner   +6 more
wiley   +1 more source

The interacting effects of precipitation and microhabitat on non‐native seed predation are contingent on temporal dynamics

open access: yesOikos, EarlyView.
Understanding how different drivers of global change interact to shape ecological processes remains a major challenge in ecology. Climate change is reshuffling the interactions that structure communities, with major implications for biological invasions.
Mariana C. Chiuffo   +4 more
wiley   +1 more source

Chromosomal and genetic anomalies in fetuses with nuchal translucency between 3.0 and 3.4 mm: A systematic review and meta-analysis. [PDF]

open access: yesActa Obstet Gynecol Scand
Fetuses with a nuchal translucency between 3.0 and 3.4 mm showed a high rate of chromosomal anomalies and copy number variants, most of which could potentially be detected through cell‐free DNA. Abstract Introduction To report the prevalence of chromosomal anomalies in fetuses with a nuchal translucency (NT) between 3.0 and 3.4 mm and to assess the ...
Carta A   +10 more
europepmc   +2 more sources

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell   +6 more
wiley   +1 more source

CMA USA

open access: yes
CMA ...
openaire   +1 more source

Business Communication: CMA 111

open access: yes, 2011
Business Communication: CMA 111, examination June ...
Osunkunle, O, Chigovanyika, M
core  

Clinical Utility of Nuchal Translucency Measurement in First‐Trimester Ultrasound Screening in a Setting With First‐Tier NIPT for Aneuploidy Screening

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective To investigate the additional clinical value of nuchal translucency (NT) measurement at the first‐trimester anomaly scan (FTAS) in a setting with first‐tier non‐invasive prenatal testing (NIPT). Method This nationwide prospective cohort study, part of the IMITAS study on FTAS implementation, included all pregnancies with increased NT
Eline E. R. Lust   +15 more
wiley   +1 more source

Structural Variation Sequencing of 26 Amniotic Fluid Samples With Partial Gene Duplications and Postnatal Follow‐Up of the Fetuses

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objectives Partial gene duplications (PGDups) are a significant contributor to genetic disease. The precise genomic location and structure of PGDups are often unresolved using conventional methods, so prenatal diagnosis for PGDups is challenging, especially without ultrasound abnormalities.
Shengfang Qin   +10 more
wiley   +1 more source

Cytogenetic and Molecular Findings in Hydrops‐Related Mirror Syndrome

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective Mirror syndrome is a rare, life‐threatening condition in which maternal fluid overload mirrors fetal hydrops. Data on genetic findings in affected pregnancies are limited. We compared genetic diagnoses in hydrops cases with and without mirror syndrome.
Brian A. Burnett   +11 more
wiley   +1 more source

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