Results 131 to 140 of about 80,799 (293)

Adapting Image‐Based Models for 1D Data via Spider Plot Transformation and Transfer Learning

open access: yesAdvanced Intelligent Systems, EarlyView.
A novel method enables the use of pretrained image‐based neural networks for complex 1D data, including Raman and mid‐infrared spectra, electrocardiograms, and mass spectrometry. 2D spider plots with false‐color fill enable transfer lerning, therefore enhancing data augmentation and model explainability across diverse spectral and time series datasets.
Azadeh Mokari   +2 more
wiley   +1 more source

E‐CAD: Electroactive Polymer‐Based Cardiac Assist Device with Low Power Consumption

open access: yesAdvanced Intelligent Systems, EarlyView.
Conventional cardiac assist devices often require high power, involve direct blood contact, and risk driveline infections. This work presents a soft electroactive polymer‐based system that compresses the heart externally while consuming <0.3 W. With no blood contact, a 0.3 mm driveline, and a compact design, E‐CAD demonstrates enhanced output and ...
Jiyeop Kim   +4 more
wiley   +1 more source

Is resynchronization between left and right ventricles responsible for improving hemodynamic function of heart failure patients with LBBB? [PDF]

open access: bronze, 2000
Yang Yu   +6 more
openalex   +1 more source

Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B‐Related Disorders: Case Series and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione   +12 more
wiley   +1 more source

Inotropic effect of some membranotropic agents on isolated right ventricle of rat heart [PDF]

open access: bronze, 2000
Maja Pavlović   +5 more
openalex   +1 more source

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong   +16 more
wiley   +1 more source

Chromosome 3q22.2‐q26.2 Interstitial Deletion in a Patient With Wisconsin Syndrome, Blepharophimosis‐Ptosis‐Epicanthus Inversus Syndrome, Dandy‐Walker Malformation, Pierre Robin Sequence, and Recurrent Infections

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun   +2 more
wiley   +1 more source

Distribution of the Muscarinic K+ Channel Proteins Kir3.1 and Kir3.4 in the Ventricle, Atrium, and Sinoatrial Node of Heart [PDF]

open access: bronze, 2001
Halina Dobrzynski   +8 more
openalex   +1 more source

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