NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Por um escritor misterioso
Last updated 22 outubro 2024
bioRxiv - the preprint server for biology, operated by Cold Spring Harbor Laboratory, a research and educational institution
Regulation of neuronal gene expression by AUTS2. a, IGV browser views
Essential role of MESP1-RING1A complex in cardiac differentiation - ScienceDirect
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain - ScienceDirect
Polycomb‐mediated gene regulation in human brain development and neurodevelopmental disorders - Bölicke - 2022 - Developmental Neurobiology - Wiley Online Library
Polycomb‐mediated gene regulation in human brain development and neurodevelopmental disorders - Bölicke - 2022 - Developmental Neurobiology - Wiley Online Library
Cerebral Organoids Containing an AUTS2 Missense Variant Model Microcephaly
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Context-specific Polycomb mechanisms in development
Frontiers AUTS2 Syndrome: Molecular Mechanisms and Model Systems
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Frontiers AUTS2 Syndrome: Molecular Mechanisms and Model Systems
An AUTS2-Polycomb complex activates gene expression in the CNS. - Abstract - Europe PMC
An AUTS2-Polycomb complex activates gene expression in the CNS. - Abstract - Europe PMC
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain - ScienceDirect
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain - ScienceDirect
Recomendado para você
-
Rubinstein-Taybi syndrome: Dental manifestations and management22 outubro 2024
-
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials22 outubro 2024
-
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect22 outubro 2024
-
Cureus, Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 722 outubro 2024
-
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes22 outubro 2024
-
Expanding the phenotype associated to KMT2A variants: overlapping22 outubro 2024
-
A novel CREBBP mutation and its phenotype in a case of Rubinstein22 outubro 2024
-
Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly22 outubro 2024
-
PDF) Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly22 outubro 2024
-
SciELO - Brasil - Prosthetic rehabilitation of a child with22 outubro 2024
você pode gostar
-
Etiqueta Escolar Léo o Caminhão Brinquedos - Imagem Legal22 outubro 2024
-
Cachepot Rosto com Óculos em Cerâmica Pêssego 11,8x9,8 cm - D'Rossi22 outubro 2024
-
hack//G.U. Trilogy22 outubro 2024
-
🎹 TODOS OS VÍDEOS de KiiYii em Português!, Desenhos Animados Dublados para Crianças, Músicas Infantis22 outubro 2024
-
ZAGREB, CROATIA - JULY 13, 2019: Croatian league Supercup, GNK Dinamo vs. HNK Rijeka. Dinamo players holding trophy and celebrating victory Stock Photo - Alamy22 outubro 2024
-
Download Auto Clicker - Automatic tap for Android - Free - 2.1.422 outubro 2024
-
Halo 2, Bungie Wiki22 outubro 2024
-
Minecraft will require a Microsoft account to play in 2021 - The Verge22 outubro 2024
-
Every Art Style Zelda Games Have Ever Had - IGN22 outubro 2024
-
Legend Of Zelda, The - A Link To The Past ROM - SNES Download22 outubro 2024