ZFIN Person: Quintana, Anita

ZFIN ID: ZDB-PERS-160721-3

Quintana, Anita

Email:	aquintana8@utep.edu
URL:	http://expertise.utep.edu/profiles/aquintana8
Affiliation:	Quintana Lab
Address:	500 West University Ave, El Paso TX 79968
Country:	United States
Phone:	915-747-8988
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Paz, D., Pinales, B.E., Castellanos, B.S., Perez, I., Gil, C.B., Madrigal, L.J., Reyes-Nava, N.G., Castro, V.L., Sloan, J.L., Quintana, A.M. (2023) Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant. Differentiation; research in biological diversity. 131:748174-81

Castro, V.L., Paz, D., Virrueta, V., Estevao, I.L., Grajeda, B.I., Ellis, C.C., Quintana, A.M. (2023) Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes. Gene. 864:147290

Castellanos, B.S., Reyes-Nava, N.G., Quintana, A.M. (2021) Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish. BMC Developmental Biology. 21:7

Castro, V.L., Reyes-Nava, N.G., Sanchez, B.B., Gonzalez, C.G., Paz, D., Quintana, A.M. (2020) Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism. Genesis (New York, N.Y. : 2000). 58(12):e23397

Castro, V.L., Reyes, J.F., Reyes-Nava, N.G., Paz, D., Quintana, A.M. (2020) Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain. BMC Neuroscience. 21:27

Reyes-Nava, N., Yu, H.C., Coughlin, C.R., Shaikh, T.H., Quintana, A.M. (2020) Abnormal expression of GABA_A receptor sub-units and hypomotility upon loss of gabra1 in zebrafish. Biology Open. 9(4):

Hernandez, J.A., Castro, V.L., Reyes-Nava, N., Montes, L.P., Quintana, A.M. (2019) Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development. Blood advances. 3:1244-1254

Quintana, A.M., Yu, H.C., Brebner, A., Pupavac, M., Geiger, E.A., Watson, A., Castro, V.L., Cheung, W., Chen, S.H., Watkins, D., Pastinen, T., Skovby, F., Appel, B., Rosenblatt, D.S., Shaikh, T.H. (2017) Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities. Human molecular genetics. 26(15):2838-2849

Quintana, A.M., Hernandez, J.A., Gonzalez, C.G. (2017) Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development. PLoS One. 12:e0180856

NON-ZEBRAFISH PUBLICATIONS