Results 221 to 230 of about 401,272 (328)

Studies on the Respiratory Chain-linked Reduced Nicotinamide Adenine Dinucleotide Dehydrogenase

, 1964
Terenzio Cremona, Edna B. Kearney
openalex   +1 more source

Autofluorescence Imaging and Virtual Histological Staining of Human Prostate Sections for Cancer Diagnosis

Advanced Intelligent Systems, EarlyView.
Autofluorescence imaging with virtual histological staining streamlines postoperative histopathology. Using a deep ultraviolet light‐emitting diode (LED)‐based imaging system and a weakly supervised deep learning model, virtual hematoxylin and eosin (H&E)‐stained images are generated from the autofluorescence of prostate tissue. Pathologist evaluations
Mingxuan Si, Weixing Dai, Ivy H. M. Wong, Yan Zhang, Tony K. F. Ma, Ping Wing Ng, Kwok Hung Li, Sylvia M. S. Wong, John H. K. Ngan, Terence T. W. Wong   +9 more
wiley   +1 more source

A novel molecular switch in plant growth: how adenosine kinase activity modulates plant development and growth pathways. [PDF]

J Exp Bot
Watson KM.
europepmc   +1 more source

Properties of Nicotinamide Adenine Dinucleotide Phosphate-Dependent Formate Dehydrogenase from Clostridium thermoaceticum [PDF]

, 1966
Lan-Fun Li, Lars G. Ljungdahl, Harland G. Wood   +2 more
openalex   +1 more source

On the Recovery of Adenine

Journal of Biological Chemistry, 1911
Walter Jones, George DeF. Barnett
openaire   +2 more sources

Phenotypical and Genotypical Expansion of Autosomal‐Dominant KDM1A‐Related Neurodevelopmental Disorder Spectrum: A Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT KDM1A‐related neurodevelopmental disorder (CPRF, OMIM #616728) is characterized by cleft palate, global developmental delay, and distinct facial gestalt, but phenotypic knowledge of this ultra‐rare autosomal dominant disorder is limited. Here, we report on a 13‐year‐old boy with a novel heterozygous, likely pathogenic germline missense variant
Sebastian Burkart, Melanie Spanjaard, Lilian Kaufmann, Katrin Hinderhofer, Christian P. Schaaf, Markus Ries, Maja Hempel   +6 more
wiley   +1 more source

Introducing the "other" type of DNA methylation. [PDF]

Sci Adv
Bochtler M.
europepmc   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Unveiling Adenine H‑bonded Hexads: Hierarchical Self-Assembly for Helical Columnar Functional Materials. [PDF]

JACS Au
Martínez-Bueno A, Valencia-Vásconez GM, Termine R, Golemme A, Ortega J, Folcia CL, Granadino-Roldán JM, Navarro A, Giménez R, Sierra T.   +9 more
europepmc   +1 more source

Uptake of Adenine Nucleotides by Respiring Mitochondria during Active Accumulation of Ca++ and Phosphate

, 1965
Ernesto Carafoli, Carlo S. Rossi, Albert L. Lehninger   +2 more
openalex   +1 more source