Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain

Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish

(2020) Nayeli G. Reyes-Nava et al.   Biology Open

Cortical and Commissural Defects Upon HCF-1 Loss in Nkx2.1 -Derived Embryonic Neurons and Glia

(2019) Shilpi Minocha et al.   Developmental Neurobiology

sox2 and sox3 cooperate to regulate otic/epibranchial placode induction in zebrafish

(2018) Yunzi Gou et al.   DEVELOPMENTAL BIOLOGY

A novel ASXL1–OGT axis plays roles in H3K4 methylation and tumor suppression in myeloid malignancies

(2018) Daichi Inoue et al.   LEUKEMIA

Loss of ASXL1 in the bone marrow niche dysregulates hematopoietic stem and progenitor cell fates

(2018) Peng Zhang et al.   Cell Discovery

Asxl1 ablation in mouse embryonic stem cells impairs neural differentiation without affecting self-renewal

(2018) SoJung An et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Role of ASXL1 mutation in impaired hematopoiesis and cellular senescence

(2018) Masahiro Uni et al.   Oncotarget

Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence

(2018) Edith Bonnin et al.   PLoS Genetics

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

(2017) Anita M. Quintana et al.   HUMAN MOLECULAR GENETICS

X-Linked Cobalamin Disorder ( HCFC1 ) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic Acid

(2017) Emmanuel Scalais et al.   PEDIATRIC NEUROLOGY

Guidelines for morpholino use in zebrafish

(2017) Didier Y. R. Stainier et al.   PLoS Genetics

Asxl1 deficiency in embryonic fibroblasts leads to cellular senescence via impairment of the AKT-E2F pathway and Ezh2 inactivation

(2017) Hye Sook Youn et al.   Scientific Reports

Epiblast-specific loss of HCF-1 leads to failure in anterior-posterior axis specification

(2016) Shilpi Minocha et al.   DEVELOPMENTAL BIOLOGY

Compensatory embryonic response to allele-specific inactivation of the murine X-linked gene Hcfc1

(2016) Shilpi Minocha et al.   DEVELOPMENTAL BIOLOGY

Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations inZNF143, Which Codes for a Transcriptional Activator

(2016) Mihaela Pupavac et al.   HUMAN MUTATION

A CRISPR/Cas9 Vector System for Tissue-Specific Gene Disruption in Zebrafish

(2015) Julien Ablain et al.   DEVELOPMENTAL CELL

HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain

(2015) L. A. Jolly et al.   HUMAN MOLECULAR GENETICS

Genomic Determinants of THAP11/ZNF143/HCFC1 Complex Recruitment to Chromatin

(2015) Aurimas Vinckevicius et al.   MOLECULAR AND CELLULAR BIOLOGY

Structures and properties of PAX linked regulatory networks architecting and pacing the emergence of neuronal diversity

(2015) Gloria G. Curto et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Mouse models of human PIK3CA-related brain overgrowth have acutely treatable epilepsy

(2015) Achira Roy et al.   eLife

Statistical Analysis of Zebrafish Locomotor Response

(2015) Yiwen Liu et al.   PLoS One

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

(2014) Dalila Pinto et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Trimmomatic: a flexible trimmer for Illumina sequence data

(2014) Anthony M. Bolger et al.   BIOINFORMATICS

Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation

(2014) Elizabeth M. Paronett et al.   CEREBRAL CORTEX

Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression

(2014) Anita M. Quintana et al.   DEVELOPMENTAL BIOLOGY

Sqstm1 knock-down causes a locomotor phenotype ameliorated by rapamycin in a zebrafish model of ALS/FTLD

(2014) Serena Lattante et al.   HUMAN MOLECULAR GENETICS

CHD8regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors

(2014) Aarathi Sugathan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Zebrafish as an emerging model for studying complex brain disorders

(2014) Allan V. Kalueff et al.   TRENDS IN PHARMACOLOGICAL SCIENCES

An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1

(2013) Hung-Chun Yu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Heat-shock-mediated conditional regulation of hedgehog/gli signaling in zebrafish

(2013) Meng-Chieh Shen et al.   DEVELOPMENTAL DYNAMICS

HCFC1 is a common component of active human CpG-island promoters and coincides with ZNF143, THAP11, YY1, and GABP transcription factor occupancy

(2013) J. Michaud et al.   GENOME RESEARCH

Structural and temporal requirements of Wnt/PCP protein Vangl2 function for convergence and extension movements and facial branchiomotor neuron migration in zebrafish

(2013) Xiufang Pan et al.   MECHANISMS OF DEVELOPMENT

Efficient genome editing in zebrafish using a CRISPR-Cas system

(2013) Woong Y Hwang et al.   NATURE BIOTECHNOLOGY

Validation of the Zebrafish Pentylenetetrazol Seizure Model: Locomotor versus Electrographic Responses to Antiepileptic Drugs

(2013) Tatiana Afrikanova et al.   PLoS One

Inducible Sterilization of Zebrafish by Disruption of Primordial Germ Cell Migration

(2013) Ten-Tsao Wong et al.   PLoS One

SOX2-LIN28/let-7 pathway regulates proliferation and neurogenesis in neural precursors

(2013) F. Cimadamore et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Towards a Comprehensive Catalog of Zebrafish Behavior 1.0 and Beyond

(2013) Allan V. Kalueff et al.   Zebrafish

TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions

(2013) Daehwan Kim et al.   GENOME BIOLOGY

A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

(2012) Lingli Huang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks

(2012) Cole Trapnell et al.   Nature Protocols

SOX2 expression levels distinguish between neural progenitor populations of the developing dorsal telencephalon

(2011) Scott R. Hutton et al.   DEVELOPMENTAL BIOLOGY

Sequentially acting Sox transcription factors in neural lineage development

(2011) M. Bergsland et al.   GENES & DEVELOPMENT

APP-dependent up-regulation of Ptch1 underlies proliferation impairment of neural precursors in Down syndrome

(2011) Stefania Trazzi et al.   HUMAN MOLECULAR GENETICS

Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management

(2011) Nuria Carrillo-Carrasco et al.   JOURNAL OF INHERITED METABOLIC DISEASE

De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome

(2011) Alexander Hoischen et al.   NATURE GENETICS

Coffin–Lowry syndrome: A role for RSK2 in mammalian neurogenesis

(2010) Chandrasagar B. Dugani et al.   DEVELOPMENTAL BIOLOGY

CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain

(2010) Jing Wang et al.   DEVELOPMENTAL CELL

Ronin/Hcf-1 binds to a hyperconserved enhancer element and regulates genes involved in the growth of embryonic stem cells

(2010) M. Dejosez et al.   GENES & DEVELOPMENT

Role of the HCF-1 Basic Region in Sustaining Cell Proliferation

(2010) Marco Mangone et al.   PLoS One

Costello syndrome H-Ras alleles regulate cortical development

(2009) Annie Paquin et al.   DEVELOPMENTAL BIOLOGY

Ronin Is Essential for Embryogenesis and the Pluripotency of Mouse Embryonic Stem Cells

(2008) Marion Dejosez et al.   CELL

High-resolution in situ hybridization to whole-mount zebrafish embryos

(2007) Christine Thisse et al.   Nature Protocols