Mot1 redistributes TBP from TATA-containing to TATA-less promoters

GE Zentner, S Henikoff - Molecular and Cellular Biology, 2013 - Taylor & Francis
The Swi2/Snf2 family ATPase Mot1 displaces TATA-binding protein (TBP) from DNA in vitro,
but the global relationship between Mot1 and TBP in vivo is unclear. In particular, how Mot1 …

Genome wide association study in goat identified novel SNPs and genes for growth

M Moaeen-ud-Din, MS Khan, RD Muner, JM Reecy - 2023 - researchsquare.com
A higher body weight at a younger age is an economically important trait for profitable goat
farming. This study was focused on the identification of regions of the genome that harbor …

[HTML][HTML] Time-dependent toxic effects of N-ethyl-N-nitrosourea on the testes of male C57BL/6J mice: a histological and ultrastructural study

J Yin, K Sun, B Chen - International journal of clinical and …, 2015 - ncbi.nlm.nih.gov
Abstract N-ethyl-N-nitrosourea (ENU), a well known alkylating agent, is a powerful mutagen
in mouse spermatogonia that is frequently used to generate mutant mice for the study of …

TAFopathies Result from Derangements in Transcriptional Regulation of Metabolism

JM Leid - 2023 - search.proquest.com
Cardiogenesis and the maintenance of cardiac physiology necessitate dynamic and
carefully coordinated transcription programs. Studies in a many systems–both in vitro and in …

[PDF][PDF] Depletion of BTAF1 inhibits Epithelial-to-mesenchymal Transition via the TGF-β Signal pathway in the osteosarcoma

T Xia, Y Yang, Z Ying, Z Wang, H Zhang - 2022 - scholar.archive.org
Osteosarcoma (OS) is one of the most malignant tumors of bone with a poor outcome in
children and young adolescents and has a poor response to radiotherapy and …

Role of Cecr2 and Candidate Modifier Genes of Cecr2 in the Neural Tube Defect Exencephaly

RYM Leduc - 2015 - era.library.ualberta.ca
Neurulation, the early developmental process that forms the rudiment of the brain and spinal
cord, relies upon the intricate interplay of hundreds of genes in multiple genetic pathways …

Mapping Genes Causing Syndromic and Non-Syndromic Human Hereditary Skin Disorders

K Shah - 2018 - repository.pastic.gov.pk
Genetic defects in complex processes of embryonic development and postnatal
maintenance of the skin and its appendages result in clinically and genetically …

[引用][C] Investigation of genetic and developmental defects in the L11Jus8 mutant mouse

C Clowes - 2012 - University of Manchester