Results 111 to 120 of about 404,078 (317)

Directed evolution of enzymes at the crossroads of tradition and innovation

open access: yesFEBS Open Bio, EarlyView.
An iterative cycle of data‐driven enzyme optimization comprising four stages: genetic diversification of a template enzyme, expression of protein variants, high‐throughput evaluation, and machine‐learning‐guided redesign of the next variant library.
Maria Tomkova   +2 more
wiley   +1 more source

Vanadia Promoted Co-AI20 3 Fischer-Tropsch Catalysts

open access: yes, 2004
Bibliography: leaves 117-124.The primary aim of this work was to study systematically V20 5 promotion on yAI203 supported cobalt-based Fischer-Tropsch catalysts.
Zwane, Seneliso T
core  

Guiding AlphaFold to predict how Munc13‐1 opens Syntaxin‐1

open access: yesFEBS Open Bio, EarlyView.
The syntaxin‐1 Habc‐domain (orange), linker (pink) and SNARE motif (yellow) form a closed conformation that binds to Munc18‐1 (violet) and is opened by the Munc13‐1 MUN domain (cyan) to form the SNARE complex that triggers neurotransmitter release.
Madhurima Chattopadhyay   +2 more
wiley   +1 more source

Aging Is a Key Driver for Adult Acute Myeloid Leukemia

open access: yesAging and Cancer, EarlyView.
Acute myeloid leukemia (AML) is a classical age‐related hematologic malignancy, and a key driver of AML is aging, which profoundly regulates intrinsic factors such as genomic instability, epigenetic reprogramming, and metabolic dysregulation, and alters bone marrow microenvironment.
Rong Yin, Haojian Zhang
wiley   +1 more source

Ir-Based Bimetallic Catalysts for Hydrogen Production through Glycerol Aqueous-Phase Reforming

open access: yes, 2018
Iridium, Iridium-Nickel and Iridium-Copper catalysts were prepared by incipient wetness impregnation and evaluated in the aqueous-phase reforming of glycerol using La2O3 or CeO2 as supports. The catalysts were characterized by N-2 physisorption, XRD, H-2-
Wenjie Shen   +11 more
core   +1 more source

Mutant NPM1 in Acute Myeloid Leukemia Initiation and Maintenance

open access: yesAging and Cancer, EarlyView.
NPM1 mutations drive acute myeloid leukemia by acting as neomorphic transcriptional regulators that cooperate with Menin–MLL and XPO1 to sustain HOX/MEIS1 expression and block differentiation. Targeting these mutant‐specific transcriptional dependencies provides a rational therapeutic strategy for NPM1‐mutated AML.
Yanan Jiang   +3 more
wiley   +1 more source

The Effect Of Catalyst Support On The Decomposition Of Methane To Hydrogen And Carbon. [PDF]

open access: yes, 2004
Decomposition of methane into carbon and hydrogen over Cu/Ni supported catalysts was investigated. The catalytic activities and the lifetimes of the catalysts were studied. Cu/Ni supported on Ti02 showed high activity and long lifetime for the reaction.
Sharif Zein, Sharif Hussein   +1 more
core  

Cinematic Catalysts

open access: yes, 2013
There is no question that at this point in time we view the world through the cinematic lens. The way we move and perceive space, time and the landscape is most certainly through this lens. How can this method be harnessed to become a methodology that is gen-erative rather than just representational?
openaire   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Prominent Movement Disorders in RNU2‐2‐Related Spliceosomopathy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Pediatric movement disorders often overlap with neurodevelopmental diseases, suggesting shared molecular mechanisms. Variants in small nuclear RNA (snRNA) genes encoding spliceosome components have recently been associated with neurodevelopmental disorders, termed “RNUopathies.” We analyzed genome sequencing data from 14 patients with ...
Magdalena Krygier   +6 more
wiley   +1 more source

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