DEAD/H-box helicases in immunity, inflammation, cell differentiation, and cell death and disease
P Samir, TD Kanneganti - Cells, 2022 - mdpi.com
DEAD/H-box proteins are the largest family of RNA helicases in mammalian genomes, and
they are present in all kingdoms of life. Since their discovery in the late 1980s, DEAD/H-box …
they are present in all kingdoms of life. Since their discovery in the late 1980s, DEAD/H-box …
WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome
Werner Syndrome (WS) is an autosomal recessive disorder characterized by premature
aging due to mutations of the WRN gene. A classical sign in WS patients is short stature, but …
aging due to mutations of the WRN gene. A classical sign in WS patients is short stature, but …
Co-Occurrence of Germline Genomic Variants and Copy Number Variations in Hereditary Breast and Colorectal Cancer Patients
L Côrtes, TR Basso, RAR Villacis, JS Souza… - Genes, 2023 - mdpi.com
Hereditary Breast and Ovarian Cancer (HBOC) syndrome is an autosomal dominant disease
associated with a high risk of developing breast, ovarian, and other malignancies. Lynch …
associated with a high risk of developing breast, ovarian, and other malignancies. Lynch …
Werner helicase is required for proliferation and DNA damage repair in multiple myeloma
Background Multiple myeloma (MM), characterized by extensive genomic instability and
aberrant DNA damage repair, is a plasma cell malignancy due to the excessive proliferation …
aberrant DNA damage repair, is a plasma cell malignancy due to the excessive proliferation …
Interacción de la proteína del Síndrome de Werner (WRN) con los ARN mensajeros (ARNM) en la línea celular HELA
VC Valle-Riestra Felice - 2021 - repositorio.urp.edu.pe
El presente trabajo tuvo como finalidad evaluar la interacción in vivo, mediante ensayos de
pull-down, de la proteína de Werner (WRN), con los ARNm totales, ambos aislados de …
pull-down, de la proteína de Werner (WRN), con los ARNm totales, ambos aislados de …
Elucidation of the Molecular Mechanisms of Werner Syndrome with Stem Cell Models
Y Tian - 2021 - search.proquest.com
Werner Syndrome (WS) is an autosomal recessive disease which is characterized by
accelerated aging phenotypes, such as short stature, dyslipidemia, the loss of subcutaneous …
accelerated aging phenotypes, such as short stature, dyslipidemia, the loss of subcutaneous …
Evaluación de los niveles de los productos génicos (ARNm y proteínas) de genes implicados en el transporte de los ARNm tras el silenciamiento de la proteína WRN …
SRM Cruz Visalaya - 2020 - repositorio.urp.edu.pe
El propósito de la presente investigación fue evaluar la existencia de un vínculo funcional
entre WRN y componentes de la maquinaria de transporte de los ARNm, que pudiera …
entre WRN y componentes de la maquinaria de transporte de los ARNm, que pudiera …