Results 201 to 210 of about 209,468 (302)

The genome sequence of the Toadflax Brocade, <i>Calophasia lunula</i> (Hufnagel, 1766) (Lepidoptera: Noctuidae). [PDF]

open access: yesWellcome Open Res
Wright CJ   +8 more
europepmc   +1 more source

Genome‐wide association and interaction analysis for proliferative retinopathy in adults with type 2 diabetes born during famine: The DOLCE study in Ukraine

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose Proliferative diabetic retinopathy (PDR) is one of the leading causes of blindness in working‐age adults. We have previously shown that the risk of PDR is significantly elevated in individuals with intrauterine exposure to famine. However, the genetic mechanisms mediating this association remain unknown.
Olena Fedotkina   +7 more
wiley   +1 more source

The genome sequence of Water Lobelia, <i>Lobelia dortmanna</i> L., 1753 (Asterales: Campanulaceae). [PDF]

open access: yesWellcome Open Res
Christenhusz MJM   +11 more
europepmc   +1 more source

Haplotyp [PDF]

open access: yes, 2018
openaire   +1 more source

Macular telangiectasia type 2 genetic risk variants associated with clinical characteristics in the Slovenian cohort

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose Early diagnosis of macular telangiectasia type 2 (MacTel) remains challenging, and the contribution of genetic variation to its clinical heterogeneity is unclear. This study investigated associations between MacTel risk variants and clinical characteristics in a Slovenian cohort.
Ajda Kunčič   +4 more
wiley   +1 more source

Somatic epimutations cap genetic determinism in the human diploid chromatin epigenome. [PDF]

open access: yesCell
Vollger MR   +27 more
europepmc   +1 more source

A genetic and historical perspective on the origins of keratitis fugax hereditaria

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To investigate the genetic and genealogical background of keratitis fugax hereditaria (KFH), a periodic corneal disease caused by the heterozygous pathogenic variant c.61G>C in the NLRP3 gene. KFH is characterized by recurrent unilateral autoinflammatory attacks alternating between the eyes and permanent corneal opacities.
Annamari T. Immonen   +7 more
wiley   +1 more source

The genome sequence of empress tree, <i>Paulownia tomentosa</i> (Thunb.) Steud. (Lamiales: Paulowniaceae). [PDF]

open access: yesWellcome Open Res
Christenhusz MJM   +11 more
europepmc   +1 more source

Genetic Engineering of Tumor‐Infiltrating Lymphocytes (TIL) via a T‐Editor Platform to Enhance Anti‐Tumor Activity

open access: yesCancer Science, EarlyView.
A rapid and efficient CRISPR‐mediated gene editing platform for TIL engineering identified FAM84B as a novel potential target to enhance antitumor activity and pioneered the use of CBE to generate FAM84B loss‐of‐function TIL with enhanced antitumor activity.
Fenge Li   +13 more
wiley   +1 more source

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