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Quintana, Anita

One or more keywords matched the following items that are connected to Quintana, Anita

Item Type	Name
Concept	Zebrafish
Concept	Zebrafish Proteins
Academic Article	Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway.
Academic Article	Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression.
Academic Article	Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development.
Academic Article	Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities.
Academic Article	Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development.
Academic Article	Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain.
Academic Article	Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development.
Academic Article	Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish.
Grant	Mutations in HCFC1 alter neural precursor differentiation
Academic Article	Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism.
Grant	MMACHC Regulates Craniofacial Development
Academic Article	Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish.
Academic Article	Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes.
Academic Article	Abnormal chondrocyte intercalation in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant.
Academic Article	Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development.
Academic Article	Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant.

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