Showing results (231-240 of 7,413) with videos related to
Sort By:
Pageof 742
Nature Genetics|April 15, 2020
Genome sequence of Gossypium herbaceum and genome updates of Gossypium arboreum and Gossypium hirsutum provide insights into cotton A-genome evolutionGai Huang, Zhiguo Wu, Richard G Percy, et al.Nature Genetics|December 17, 1997
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domainsNature Genetics|December 17, 1997
Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disordersH Portsteffen, A Beyer, E Becker, et al.Nature Genetics|December 17, 1997
Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathwaysC Barlow, K D Brown, C X Deng, et al.Nature Genetics|December 17, 1997
Genetic interaction between PARP and DNA-PK in V(D)J recombination and tumorigenesisC Morrison, G C Smith, L Stingl, et al.Nature Genetics|May 18, 2021
CTCF mediates dosage- and sequence-context-dependent transcriptional insulation by forming local chromatin domainsHui Huang, Quan Zhu, Adam Jussila, et al.Nature Genetics|August 3, 2021
Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobinPhillip A Doerfler, Ruopeng Feng, Yichao Li, et al.Nature Genetics|June 24, 2020
Cohesin promotes stochastic domain intermingling to ensure proper regulation of boundary-proximal genesJennifer M Luppino, Daniel S Park, Son C Nguyen, et al.Nature Genetics|December 28, 2004
The Arabidopsis thaliana MEDEA Polycomb group protein controls expression of PHERES1 by parental imprintingClaudia Köhler, Damian R Page, Valeria Gagliardini, et al.Nature Genetics|December 28, 2004
Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivityPascal Descargues, Céline Deraison, Chrystelle Bonnart, et al.Pageof 742