Publicaciones
| 2005 | Uauy R, Rojas C, Llanos A, Mena P. Dietary essential fatty acids in early postnatal life: Long-term outcomes. In: Hornstra G, Uauy R, Yang X., editors. The impact of maternal nutrition on the offspring. Basel: Nestec Ltd, Vevey and S. Karger; 2005. p.101-136 (Nestlé Nutrition Workshop Series. Pediatric Program; v.55) |
| 2003 | Minguell JJ, Erices A, Conget PA, Sierralta WD, Rojas CV, Allers C,Benavente C, Fierro F, Rivera F. Mesenchymal (uncommitted) stem cells. In: Miñana Grisolia MD, Bendala-Tufanisco E., editors. Mesenchymal stem cells: biology and potential clinical uses. Madrid: Fundación Valenciana de Estudios Avanzados; 2003. p.13-36 |
| 2015 | Palominos MM, Dünner NH, Wabitsch M, Rojas CV. Angiotensin II directly impairs adipogenic differentiation of human preadipose cells. Mol Cell Biochem 2015; 408(1-2):115-122 |
| 2013 | Dünner N, Quezada C, Berndt FA, Cánovas J, Rojas CV. Angiotensin II signaling in human preadipose cells: participation of ERK1,2-dependent modulation of Akt. PLoS One 2013 Oct 2;8(10):e75440 |
| 2010 | Behrens MI, Brüggemann N, Chana P, Venegas P, Kägi M, Parrao T, Orellana P, Garrido CM, Rojas CV, Hauke J, Hahnen E, González R, Seleme N, Fernández V, Binkofski, Kömpf D, Kubisch C, Hagenah J, Klein C, Ramírez A. Clinical spectrum of Kufor Rakeb syndrome in the Chilean kindred with ATP13A2 mutations. Mov Disord 2010; 25(12):1929-1937 |
| 2010 | Villavicencio A, Aguilar G, Argüello G, Dünner C, Gabler F, Soto E, Gaete F, Peñaloza P, Celis M, Rojas C. The effect of overweight and obesity on proliferation and activation of AKT and ERK in human endometria. Gynecol Oncol 2010; 117(1):96-102 |
| 2010 | Cifuentes M, Mattar P, Fuentes C, Tobar N, Hugo E, Ben-Jonathan N, Rojas C, Martinez J. Obesity-associated proinflammatory cytokines increase calcium sensing receptor (CaSR) protein expression in primary human adipocytes and LS14 human adipose cell line. Arch Biochem Biophys 2010; 500(2):151-156 |
| 2010 | Fuentes P, Acuña MJ, Cifuentes M, Rojas CV. The anti-adipogenic effect of angiotensin II on human preadipose cells involves ERK1,2 activation. J Endocrinol 2010; 206 (1): 75-83 |
| 2008 | Cifuentes M, Rojas CV. Antilipolytic effect of calcium-sensing receptor in human adipocytes. Mol Cell Biochem 2008; 319(1-2):17-21 |
| 2007 | Brucher R, Cifuentes M, Acuña MJ, Albala C, Rojas CV. Larger anti-adipogenic effect of angiotensin II on omental preadipose cells of obese humans. Obesity (Silver Spring) 2007; 15(7):1643-1646 |
| 2005 | Cifuentes M, Albala C, Rojas C. Calcium-sensing receptor expression in human adipocytes. Endocrinology 2005; 146(5):2176-2179 |
| 2004 | Santa Maria L, Rojas CV, Minguell JJ. Signals from damaged but not undamaged skeletal muscle induce myogenic differentiation of rat bone-marrow-derived mesenchymal stem cells. Exp Cell Res 2004; 300(2):418-426 |
| 2003 | Santa María LI, Rojas CV, Alliende MA, Santos JL. Linkage analysis suggests a genetic defect in CNGB3 gene causing Complete Achromatopsia in a Chilean consanguineous family. BAG Basic Appl Genet 2003; 15:9-13 |
| 2003 | Rojas C, Martínez J, Flores I, Hoffman DR, Uauy R. Gene expression analysis in human fetal retinal explants treated with docosahexaenoic acid. Invest Ophthalmol Vis Sci 2003; 44(7):3170-3177 |
| 2003 | Erices A, Allers C, Conget P, Rojas C, Minguell J. Human cord blood-derived mesenchymal stem cells home and survice in the marrow of immunodeficient mice after systemic infusion. Cell Transplant 2003; 12(6):555-561 |
| 2003 | Kukuljan M, Taylor A, Chouinard H, Olguin P, Rojas C, Ribera AB. Selective regulation of xSlo splice variants during Xenopus embryogenesis. J Neurophysiol 2003; 90(5):3352-3360 |
| 2002 | Rojas C, Greiner RS, Fuenzalida LC, Martínez J, Salem N Jr, Uauy R. Long-term n-3 FA deficiency modifies peroxisome proliferator-activated receptor beta mRNA abundance in rat ocular tissues. Lipids 2002; 37(4):367-374 |
| 2002 | Rojas C, Santa Maria L, Santos JL, Cortes F, Alliende MA. A frameshift insertion in the cone cyclic nucleotide gated cation channel causes complete achromatopsia in a consanguineous family from a rural isolate. Eur J Hum Genet 2002; 10(10):638-642 |
| 2002 | Erices A, Conget P, Rojas C, Minguell J. Gp 130 activation by soluble interleukin-6 receptor/interleukin-6 enhances osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells. Exp Cell Res 2002; 280(1):24-32 |
| 2000 | Uauy R, Mena P, Rojas C. Essential fatty acid metabolism in the micropemie. Clin Perinatol 2000; 27(1): 71-93 |
| 2000 | Uauy R, Mena P, Rojas C. Essential fatty acids in early life: structural and functional role. Proc Nutr Soc 2000; 59(1):3-15 |
| 1999 | Rojas C, Neely A, Velasco-Loyden G, Palma V, Kukuljan M. Hyperkalemic periodic paralysis M1592V mutation modifies activation in human skeletal muscle Na + channel. Am J Physiol 1999; 276(1 Ip):C259-C266 |
| 1996 | Rojas C. Ion channels and human genetic diseases. News Physiol Sci 1996; 11:36-42 |
| 2008 | Cifuentes M, Albala C, Rojas CV. Differences in lipogenesis and lipolysis in obese and non-obese adult human adipocytes. Biol Res 2008;41(2):197-204 |
| 2006 | Ramíres A, Díaz V, Rojas CV, Behrens MI, Kubisch C. Migraña con aura: Una mirada molecular a un problema hereditario (Migraine with aura: a molecular view to an inherited problem). Rev Chil Neuro–Psiquiatr 2006; 44(2):98-104 |
| 2001 | Santa Maria L, Curotto B, Cortes F, Rojas C, Alliende MA. Diagnóstico molecular de los síndromes de Prader Willi y Angelman: test de metilación, citogenética y FISH (Methylation, cytogenetic and FISH tests in the molecular diagnosis of Prader-Willi and Angelman syndrome). Rev Med Chil 2001; 129:367-374 |
| 2000 | Uauy R, Martinez J, Rojas C. Bases moleculares de la regulación del metabolismo de lípidos: papel del sistema PPAR (Molecular nutrition, role of the PPAR system in lipidic metabolism and its importance in obesity and diabetes mellitus). Rev Med Chil 2000; 128:437-446 |
| 1998 | Alliende MA, Valiente A, Urzua B, Cortes F, Curotto B, Rojas C. Análisis molecular directo de mutaciones en el gen FMR-1 en pacientes con síndrome de Xq frágil y sus familias (Direct molecular analysis of FMR-1 gene mutation in patients with fragile Xq syndrome and their families). Rev Med Chil 1998; 126:1435-1446 |
| 2006 | Ramírez A, Díaz V, Rojas CV, Behrens MI, Kubisch C. Migraña con aura: Una mirada molecular a un problema hereditario (Migraine with aura: a molecular view to an inherited problem). Rev Chil Neuro–Psiquiatr 2006; 44 (2):98-104 |