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

Rapid recapitulation of non-alcoholic steatohepatitis upon loss of HCF-1 function in mice

(2018) Shilpi Minocha et al.   MOLECULAR AND CELLULAR BIOLOGY

Nkx2.1 regulates the generation of telencephalic astrocytes during embryonic development

(2017) Shilpi Minocha 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

Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorder

(2015) M. Gérard et al.   European Journal of Medical Genetics

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

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

Interaction of MYC with host cell factor-1 is mediated by the evolutionarily conserved Myc box IV motif

(2015) L R Thomas et al.   ONCOGENE

Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation

(2015) Shilpi Minocha et al.   Nature Communications

NG2 glia are required for vessel network formation during embryonic development

(2015) Shilpi Minocha et al.   eLife

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

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

Two specific populations of GABAergic neurons originating from the medial and the caudal ganglionic eminences aid in proper navigation of callosal axons

(2013) Mathieu Niquille et al.   Developmental Neurobiology

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

A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

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

O-GlcNAc Transferase/Host Cell Factor C1 Complex Regulates Gluconeogenesis by Modulating PGC-1α Stability

(2012) Hai-Bin Ruan et al.   Cell Metabolism

The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development

(2012) Carine Benadiba et al.   PLoS Genetics

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

Current concepts of polymicrogyria

(2010) A. James Barkovich   NEURORADIOLOGY

Neuronal migration disorders

(2009) Renzo Guerrini et al.   NEUROBIOLOGY OF DISEASE

Many roads lead to primary autosomal recessive microcephaly

(2009) Angela M. Kaindl et al.   PROGRESS IN NEUROBIOLOGY

Primary microcephaly: do all roads lead to Rome?

(2009) Gemma K. Thornton et al.   TRENDS IN GENETICS

Genetics and Biology of Microcephaly and Lissencephaly

(2009) Ganeshwaran H. Mochida   Seminars in Pediatric Neurology

Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C

(2009) Mathieu Niquille et al.   PLOS BIOLOGY

Fate mapping Nkx2.1-lineage cells in the mouse telencephalon

(2007) Qing Xu et al.   JOURNAL OF COMPARATIVE NEUROLOGY