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Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development

PloS one, 2017-07, Vol.12 (7), p.e0180856-e0180856

2017

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

American journal of human genetics, 2013-09, Vol.93 (3), p.506-514

2013

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Identification and regulation of c-Myb target genes in MCF-7 cells

BMC cancer, 2011-01, Vol.11 (1), p.30-30, Article 30

2011

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Leading by example: developing mentoring strategies to promote diversity and student success

Molecular biology of the cell, 2021-12, Vol.32 (22), p.vo1

2021

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

BMC neuroscience, 2020-06, Vol.21 (1), p.27-27, Article 27

2020

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

Biology open, 2020-04, Vol.9 (4)

2020

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Abnormal expression of GABAA receptor sub-units and hypomotility upon loss of gabra1 in zebrafish

Biology open, 2020-01

2020

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Dramatic repositioning of c-Myb to different promoters during the cell cycle observed by combining cell sorting with chromatin immunoprecipitation

PloS one, 2011-02, Vol.6 (2), p.e17362

2011

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Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development

Human molecular genetics, 2015-08, Vol.24 (15), p.4443-4453

2015

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Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K

The Journal of experimental medicine, 2012-03, Vol.209 (3), p.463-470

2012

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Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes

Gene, 2023-05, Vol.864, p.147290-147290, Article 147290

2023

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Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway

Disease models & mechanisms, 2014-02, Vol.7 (2), p.265-270

2014

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Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish

BMC developmental biology, 2021-03, Vol.21 (1), p.7-7, Article 7

2021

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ATF4‐dependent increase in mitochondrial‐endoplasmic reticulum tethering following OPA1 deletion in skeletal muscle

Journal of cellular physiology, 2024-04, Vol.239 (4), p.e31204-n/a

2024

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

Human molecular genetics, 2017-08, Vol.26 (15), p.2838-2849

2017

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Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development

Differentiation (London), 2024-07, Vol.138, p.100790, Article 100790

2024

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Cover Image, Volume 239, Number 4, April 2024

Journal of cellular physiology, 2024-04, Vol.239 (4), p.n/a

2024

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Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant

Differentiation (London), 2023-05, Vol.131, p.74-81

2023

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Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism

Genesis (New York, N.Y. : 2000), 2020-12, Vol.58 (12), p.e23397-n/a

2020

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

Developmental biology, 2014-12, Vol.396 (1), p.94-106

2014

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

Biology open, 2020-04, Vol.9 (4)

2020

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A focus on polarity: Investigating the role of orientation cues in mediating student performance on mRNA synthesis tasks in an introductory cell and molecular biology course

Biochemistry and molecular biology education, 2017-11, Vol.45 (6), p.501-508

2017

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Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development

Blood advances, 2019-04, Vol.3 (8), p.1244-1254

2019

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Characterization of the zebrafish gabra1 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development

Differentiation (London), 2024-07, Vol.138, p.100790, Article 100790

2024

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Cover Image, Volume 239, Number 4, April 2024

Journal of cellular physiology, 2024-04, Vol.239 (4), p.n/a

2024

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Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development

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

Identification and regulation of c-Myb target genes in MCF-7 cells

Leading by example: developing mentoring strategies to promote diversity and student success

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

Abnormal expression of GABAA receptor sub-units and hypomotility upon loss of gabra1 in zebrafish

Dramatic repositioning of c-Myb to different promoters during the cell cycle observed by combining cell sorting with chromatin immunoprecipitation

Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development

Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K

Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes

Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway

Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish

ATF4‐dependent increase in mitochondrial‐endoplasmic reticulum tethering following OPA1 deletion in skeletal muscle

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

Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development

Cover Image, Volume 239, Number 4, April 2024

Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant

Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism

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

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

A focus on polarity: Investigating the role of orientation cues in mediating student performance on mRNA synthesis tasks in an introductory cell and molecular biology course

Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development

Characterization of the zebrafish gabra1 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development

Cover Image, Volume 239, Number 4, April 2024

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