Results 161 to 170 of about 3,176,468 (279)

Rapid Discovery of Sequence‐Encoded Magnetically Reconfigurable Microrobots Using Monte Carlo Simulations

open access: yesAdvanced Intelligent Systems, EarlyView.
A Monte Carlo simulation framework is introduced to predict the folding behavior of sequence‐encoded magnetic microrobots, enabling systematic exploration of their design space. By mapping key metrics such as radius of gyration and symmetry, the framework identifies functional sequences and predicts actuation behaviors.
Collin C. Kemper   +5 more
wiley   +1 more source

The Letter from the Editor

open access: yesKONA Powder and Particle Journal, 2014
Mojtaba Ghadiri
doaj   +1 more source

Kata Pengantar

open access: yesAgrointek, 2021
Editorial Editorial Board
doaj   +1 more source

Journal of the Society of Motion Picture Engineers — Editorial Board [PDF]

open access: bronze, 1940
Sylvan Harris   +29 more
openalex   +1 more source

Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The gamma‐tubulin ring complex (γ‐TuRC) plays a role in coordinating centrosome and spindle pole body formation during cell division. TUBG1 encodes a critical component of the γ‐TuRC. Pathogenic TUBG1 variants can cause a range of alterations in cortical gyral patterning, microcephaly, and other neurological manifestations.
Roser Urreizti   +12 more
wiley   +1 more source

Perspectives on the Current and Future State of Artificial Intelligence in Medical Genetics

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Artificial intelligence (AI) is rapidly transforming numerous aspects of daily life, including clinical practice and biomedical research. In light of this rapid transformation, and in the context of medical genetics, we assembled a group of leaders in the field to respond to the question about how AI is affecting, and especially how AI will ...
Benjamin D. Solomon   +20 more
wiley   +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

Editorial

open access: yesTürk Oftalmoloji Dergisi, 2017
Özlem Yıldırım
doaj   +2 more sources

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