Year |
Citation |
Score |
2023 |
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. 147290. PMID 36804358 DOI: 10.1016/j.gene.2023.147290 |
0.355 |
|
2020 |
Reyes-Nava N, Yu HC, Coughlin CR, Shaikh TH, Quintana AM. Abnormal expression of GABAA receptor sub-units and hypomotility upon loss of gabra1 in zebrafish. Biology Open. PMID 34004700 DOI: 10.1242/bio.051367 |
0.331 |
|
2020 |
Castro VL, Reyes JF, Reyes-Nava NG, Paz D, Quintana AM. Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain. Bmc Neuroscience. 21: 27. PMID 32522152 DOI: 10.1186/s12868-020-00577-1 |
0.418 |
|
2020 |
Reyes-Nava N, Yu HC, Coughlin CR, Shaikh TH, Quintana AM. Abnormal expression of GABA receptor sub-units and hypomotility upon loss of in zebrafish. Biology Open. PMID 32205311 DOI: 10.1242/Bio.051367 |
0.324 |
|
2019 |
Hernandez JA, Castro VL, Reyes-Nava N, Montes LP, Quintana AM. Mutations in the zebrafish gene reveal a novel function for isoprenoids during red blood cell development. Blood Advances. 3: 1244-1254. PMID 30987969 DOI: 10.1182/bloodadvances.2018024539 |
0.318 |
|
2017 |
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. Human Molecular Genetics. PMID 28449119 DOI: 10.1093/Hmg/Ddx157 |
0.377 |
|
2014 |
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. Developmental Biology. 396: 94-106. PMID 25281006 DOI: 10.1016/J.Ydbio.2014.09.026 |
0.313 |
|
2014 |
Quintana AM, Picchione F, Klein Geltink RI, Taylor MR, Grosveld GC. Zebrafish ETV7 regulates red blood cell development through the cholesterol synthesis pathway. Disease Models & Mechanisms. 7: 265-70. PMID 24357328 DOI: 10.1242/Dmm.012526 |
0.487 |
|
2012 |
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 p85α subunit of PI3K. The Journal of Experimental Medicine. 209: 463-70. PMID 22351933 DOI: 10.1084/Jem.20112533 |
0.417 |
|
2011 |
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. 6: e17362. PMID 21364958 DOI: 10.1371/Journal.Pone.0017362 |
0.705 |
|
2011 |
Quintana AM, Liu F, O'Rourke JP, Ness SA. Identification and regulation of c-Myb target genes in MCF-7 cells. Bmc Cancer. 11: 30. PMID 21261996 DOI: 10.1186/1471-2407-11-30 |
0.642 |
|
2011 |
Quintana AM, Ness SA. Abstract 2157: Cell cycle dependent regulation of c-Myb target gene specificity Cancer Research. 71: 2157-2157. DOI: 10.1158/1538-7445.Am2011-2157 |
0.712 |
|
2010 |
Quintana AM, Pena JJ, Ness SA. Abstract 4967: Changes in c-Myb specificity and activities during the cell cycle in T-ALL and AML Cancer Research. 70: 4967-4967. DOI: 10.1158/1538-7445.Am10-4967 |
0.706 |
|
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