Results 271 to 280 of about 3,454,386 (367)

Phase-separated super-enhancers confer an innate radioresistance on genomic DNA. [PDF]

J Radiat Res
Matsumoto K, Ikliptikawati DK, Makiyama K, Mochizuki K, Tobita M, Kobayashi I, Voon DC, Lim K, Ogawa K, Kashiwakura I, Suzuki HI, Yoshino H, Wong RW, Hazawa M.   +13 more
europepmc   +1 more source

Protein, cDNA, and genomic DNA sequences of the towel gourd trypsin inhibitor. A squash family inhibitor.

, 1993
Hui‐Lin Ma, Hongyan Qi, Chi Chen
openalex   +1 more source

A fast word search algorithm for the representation of sequence similarity in genomic DNA [PDF]

, 1994
C. Lefèvre, J.-E. Ikeda
openalex   +1 more source

Endogenous DNA Damage as a Source of Genomic Instability in Cancer

Cell, 2017
Anthony Tubbs, A. Nussenzweig
semanticscholar   +1 more source

FGF14 GAA Intronic Expansion in Unsolved Adult‐Onset Ataxia in the Care4Rare Canada Consortium

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Spinocerebellar ataxias (SCA) represent a clinically and genetically heterogeneous group of progressive neurodegenerative diseases with prominent cerebellar atrophy. Recently, a novel pathogenic repeat expansion in intron 1 of FGF14 was identified, causing adult‐onset SCA (SCA27B). We aimed to determine the proportion
Alexanne Cuillerier, Giulia F. Del Gobbo, Layla Mackay, Erika Wall, Madeline Couse, Laura M. McDonell, Mireille Cloutier, Matt C. Danzi, Jodi Warman‐Chardon, Pierre R. Bourque, Oksana Suchowersky, Alan Mears, Luke Seldenthuis, Wendy Mears, Laura Larrigan, Alexandre White‐Brown, Gerald Pfeffer, Dennis E. Bulman, David Dyment, Care4Rare Canada Consortium, Kym M. Boycott   +20 more
wiley   +1 more source

Alpha-synuclein modulates the repair of genomic DNA double-strand breaks in a DNA-PK_cs-regulated manner. [PDF]

Neurobiol Dis
Rose EP, Osterberg VR, Gorbunova V, Unni VK.   +3 more
europepmc   +1 more source

Detection of Genomic DNA with a High Sensitivity in Tissue Sections Using a Two Step Cycling In Situ PCR Procedure.

, 1994
Mihoko Morita, Hiroshi Hachisuka, Yoichiro Sasai   +2 more
openalex   +2 more sources

Genomic DNA collection.

, 2015
A. Beth, J. C. Soo, K. Anna, V. Rita, C. Brandon, A. HollandLisa, A. Kei, L. Susan, A. Joel, K. Christopher, Yalavarthy Samarasa, B. Rita, Lukomski Slawomir   +12 more
semanticscholar   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

Method for isolation of high molecular weight genomic DNA from Botryococcus biomass. [PDF]

PLoS One
Cornejo-Corona I, Boland DJ, Devarenne TP.   +2 more
europepmc   +1 more source