Results 211 to 220 of about 1,357,403 (269)

51st annual meeting of ICBDSR: data that counts - transforming lives through birth defects surveillance. [PDF]

J Community Genet
Malherbe H, Kalk E, Botto LD, Mellado C, Thomas MA, Rissmann A.   +5 more
europepmc   +1 more source

Polarization‐resolved femtosecond Vis/IR spectroscopy tailored for resolving weak signals in biological samples using minimal sample volume

FEBS Open Bio, EarlyView.
Unique biological samples, such as site‐specific mutant proteins, are available only in limited quantities. Here, we present a polarization‐resolved transient infrared spectroscopy setup with referencing to improve signal‐to‐noise tailored towards tracing small signals. We provide an overview of characterizing the excitation conditions for polarization‐
Clark Zahn, Karsten Heyne
wiley   +1 more source

Editor's Note: Protective effects of antidepressant citalopram against abnormal APP processing and amyloid beta-induced mitochondrial dynamics, biogenesis, mitophagy and synaptic toxicities in Alzheimer's disease. [PDF]

Hum Mol Genet
europepmc   +1 more source

Efficient Plasmid-Based Rescue of T7 RNA Polymerase-Driven Calicivirus Reverse Genetics Systems in Mammalian Cells Using Vaccinia Virus RNA-Capping Enzymes. [PDF]

Viruses
Buchanan FJT, Loi M, Chim C, Zhou S, Penrice-Randal R, Neves LX, Erdmann M, Emmott E.   +7 more
europepmc   +1 more source

Publisher Correction: Multi-ancestry genome-wide association analyses of refractive error augment genetic discovery and polygenic prediction. [PDF]

Nat Genet
Cheng FF, Liu X, Mi H, Wang L, Ma R, Guo Y, Sidorenko J, Jiang C, Islam T, Meguro A, Hikino K, Ishikawa Y, Tang S, Li T, Chen R, Wang L, Mägi R, Metspalu A, Estonian Biobank Research Team, 23andMe Research Team, Takeuchi M, Mizuki N, Choquet H, Jin ZB, Chen G, Zhou K, Terao C, Zeng J, Yang J.   +28 more
europepmc   +1 more source

Hereditary gastric cancer checks its balance at the ATM: Broadening risk beyond CDH1. [PDF]

Eur J Hum Genet
Lott PC, Carvajal-Carmona LG.
europepmc   +1 more source

Publisher Correction: Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder. [PDF]

Nat Genet
Greene D, Mendez R, Lees J, Barbosa M, Bruselles A, Chiriatti L, Ferraro F, Mancini C, Schot R, Sleutels F, Bertini E, Bonner DE, Bouman A, Brooks AS, Cassini THA, Ezell KM, Gomez-Ospina N, Kleefstra T, O'Donoghue M, Rives L, Shashi V, Spillmann RC, Wafik M, Undiagnosed Diseases Network, Freson K, Barakat TS, Tartaglia M, Bernstein JA, Mumford AD, Wheeler MT, Turro E.   +30 more
europepmc   +1 more source

Clinically Translatable Mutation-Based Biomarkers in Ascending Aortic Aneurysm: A Bibliometric Study. [PDF]

Hum Mutat
Yang F, Yang T, Xie X, Yang Q, Wang F.
europepmc   +1 more source

Retraction of: Genome Report: Long read, high-coverage reference genomes of the Nymphalid butterflies Catonephele acontius and Catonephele numilia (Nymphalidae: Biblidinae). [PDF]

G3 (Bethesda)
europepmc   +1 more source

Retraction: Breast cancer cell-derived exosome-delivered microRNA-155 targets UBQLN1 in adipocytes and facilitates cancer cachexia-related fat loss. [PDF]

Hum Mol Genet
europepmc   +1 more source