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Anita Quintana

TitleDr.
Faculty RankAssistant Professor
InstitutionUniversity of Texas at El Paso
DepartmentBiology
Address500 WEST UNIVERSITY
5.150 Bioscience Research Building
El Paso TX 79968
Phone9157478988
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    Collapse Research 
    Collapse research activities and funding
    F31HL090024     (QUINTANA, ANITA M)Aug 6, 2007 - Jul 31, 2011
    NIH
    Post-translational modifications affect c-Myb specificity.
    Role: Principal Investigator
    K01NS099153     (QUINTANA, ANITA M)Sep 1, 2017 - Aug 31, 2021
    NIH
    Mutations in HCFC1 alter neural precursor differentiation
    Role: Principal Investigator
    R03DE029517     (QUINTANA, ANITA M)Jan 1, 2020 - Dec 31, 2022
    NIH
    MMACHC Regulates Craniofacial Development
    Role: Principal Investigator

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Vue Z, Garza-Lopez E, Neikirk K, Katti P, Vang L, Beasley H, Shao J, Marshall AG, Crabtree A, Murphy AC, Jenkins BC, Prasad P, Evans C, Taylor B, Mungai M, Killion M, Stephens D, Christensen TA, Lam J, Rodriguez B, Phillips MA, Daneshgar N, Koh HJ, Koh A, Davis J, Devine N, Saleem M, Scudese E, Arnold KR, Vanessa Chavarin V, Daniel Robinson R, Chakraborty M, Gaddy JA, Sweetwyne MT, Wilson G, Zaganjor E, Kezos J, Dondi C, Reddy AK, Glancy B, Kirabo A, Quintana AM, Dai DF, Ocorr K, Murray SA, Damo SM, Exil V, Riggs B, Mobley BC, Gomez JA, McReynolds MR, Hinton A. 3D reconstruction of murine mitochondria reveals changes in structure during aging linked to the MICOS complex. Aging Cell. 2023 Dec; 22(12):e14009. PMID: 37960952.
      Citations: 2     Fields:    Translation:AnimalsCells
    2. Paz D, Reyes-Nava NG, Pinales BE, Perez I, Gil CB, Gonzales AV, Grajeda B, Estevao IL, Ellis CC, Castro VL, Quintana AM. Characterization of the zebrafish gabra1sa43718/sa43718 germline loss of function allele confirms a function for Gabra1 in motility and nervous system development. bioRxiv. 2023 Sep 25. PMID: 36747751.
      Citations:    
    3. Paz D, Pinales BE, Castellanos BS, Perez I, Gil CB, Madrigal LJ, Reyes-Nava NG, Castro VL, Sloan JL, Quintana AM. Abnormal chondrocyte development in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant. Differentiation. 2023 May-Jun; 131:74-81. PMID: 37167860.
      Citations: 1     Fields:    Translation:AnimalsCells
    4. Castro VL, Paz D, Virrueta V, Estevao IL, Grajeda BI, Ellis CC, Quintana AM. Missense and nonsense mutations of the zebrafish hcfc1a gene result in contrasting mTor and radial glial phenotypes. Gene. 2023 May 15; 864:147290. PMID: 36804358.
      Citations: 1     Fields:    Translation:AnimalsCells
    5. Paz D, Pinales BE, Castellanos BS, Perez I, Gil CB, Madrigal LJ, Reyes-Nava NG, Castro VL, Sloan JL, Quintana AM. Abnormal chondrocyte intercalation in a zebrafish model of cblC syndrome restored by an MMACHC cobalamin binding mutant. bioRxiv. 2023 Jan 21. PMID: 36711998.
      Citations:    
    6. Quintana AM. Leading by example: developing mentoring strategies to promote diversity and student success. Mol Biol Cell. 2021 12 01; 32(22):vo1. PMID: 34735267.
      Citations:    Fields:    Translation:Humans
    7. Castellanos BS, Reyes-Nava NG, Quintana AM. Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish. BMC Dev Biol. 2021 03 08; 21(1):7. PMID: 33678174.
      Citations: 3     Fields:    Translation:Animals
    8. Castro VL, Reyes-Nava NG, Sanchez BB, Gonzalez CG, Paz D, Quintana AM. Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism. Genesis. 2020 12; 58(12):e23397. PMID: 33197123.
      Citations: 5     Fields:    Translation:AnimalsCells
    9. Castro VL, Quintana AM. The role of HCFC1 in syndromic and non-syndromic intellectual disability. Med Res Arch. 2020 Jun; 8(6). PMID: 34164576.
      Citations:    
    10. Castro VL, Reyes JF, Reyes-Nava NG, Paz D, Quintana AM. Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain. BMC Neurosci. 2020 06 10; 21(1):27. PMID: 32522152.
      Citations: 3     Fields:    Translation:AnimalsCells
    11. Reyes-Nava NG, Yu HC, Coughlin CR, Shaikh TH, Quintana AM. Abnormal expression of GABAA receptor subunits and hypomotility upon loss of gabra1 in zebrafish. Biol Open. 2020 04 13; 9(4). PMID: 32205311.
      Citations: 8     Fields:    Translation:HumansAnimalsCells
    12. Hernandez JA, Castro VL, Reyes-Nava N, Montes LP, Quintana AM. Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development. Blood Adv. 2019 04 23; 3(8):1244-1254. PMID: 30987969.
      Citations: 5     Fields:    Translation:AnimalsCells
    13. Quintana AM, Yu HC, Brebner A, Pupavac M, Geiger EA, Watson A, Castro VL, Cheung W, Chen SH, Watkins D, Pastinen T, Skovby F, Appel B, Rosenblatt DS, Shaikh TH. Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities. Hum Mol Genet. 2017 08 01; 26(15):2838-2849. PMID: 28449119.
      Citations: 21     Fields:    Translation:HumansAnimalsCells
    14. Quintana AM, Hernandez JA, Gonzalez CG. Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development. PLoS One. 2017; 12(7):e0180856. PMID: 28686747.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    15. Olimpo JT, Quijas DA, Quintana AM. 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. Biochem Mol Biol Educ. 2017 Nov; 45(6):501-508. PMID: 28520272.
      Citations:    Fields:    Translation:Humans
    16. Quintana AM. The necessity for in vivo functional analysis in human medical genetics. Med Res Arch. 2015 Nov; 2(8). PMID: 26989768.
      Citations:    
    17. Van Laarhoven PM, Neitzel LR, Quintana AM, Geiger EA, Zackai EH, Clouthier DE, Artinger KB, Ming JE, Shaikh TH. Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development. Hum Mol Genet. 2015 Aug 01; 24(15):4443-53. PMID: 25972376.
      Citations: 87     Fields:    Translation:HumansAnimals
    18. Quintana AM, Geiger EA, Achilly N, Rosenblatt DS, Maclean KN, Stabler SP, Artinger KB, Appel B, Shaikh TH. Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression. Dev Biol. 2014 Dec 01; 396(1):94-106. PMID: 25281006.
      Citations: 19     Fields:    Translation:HumansAnimalsCells
    19. Quintana AM, Picchione F, Klein Geltink RI, Taylor MR, Grosveld GC. Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway. Dis Model Mech. 2014 Feb; 7(2):265-70. PMID: 24357328.
      Citations: 12     Fields:    Translation:HumansAnimalsCells
    20. Yu HC, Sloan JL, Scharer G, Brebner A, Quintana AM, Achilly NP, Manoli I, Coughlin CR, Geiger EA, Schneck U, Watkins D, Suormala T, Van Hove JL, Fowler B, Baumgartner MR, Rosenblatt DS, Venditti CP, Shaikh TH. An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1. Am J Hum Genet. 2013 Sep 05; 93(3):506-14. PMID: 24011988.
      Citations: 58     Fields:    Translation:HumansCells
    21. Conley ME, Dobbs AK, Quintana AM, Bosompem A, Wang YD, Coustan-Smith E, Smith AM, Perez EE, Murray PJ. Agammaglobulinemia and absent B lineage cells in a patient lacking the p85a subunit of PI3K. J Exp Med. 2012 Mar 12; 209(3):463-70. PMID: 22351933.
      Citations: 87     Fields:    Translation:HumansAnimalsCells
    22. Quintana AM, Zhou YE, Pena JJ, O'Rourke JP, Ness SA. Dramatic repositioning of c-Myb to different promoters during the cell cycle observed by combining cell sorting with chromatin immunoprecipitation. PLoS One. 2011 Feb 22; 6(2):e17362. PMID: 21364958.
      Citations: 19     Fields:    Translation:HumansCells
    23. Quintana AM, Liu F, O'Rourke JP, Ness SA. Identification and regulation of c-Myb target genes in MCF-7 cells. BMC Cancer. 2011 Jan 25; 11:30. PMID: 21261996.
      Citations: 49     Fields:    Translation:HumansCells
    24. Ortega JL, Moguel-Esponda S, Potenza C, Conklin CF, Quintana A, Sengupta-Gopalan C. The 3' untranslated region of a soybean cytosolic glutamine synthetase (GS1) affects transcript stability and protein accumulation in transgenic alfalfa. Plant J. 2006 Mar; 45(5):832-46. PMID: 16460515.
      Citations: 19     Fields:    Translation:AnimalsCells
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