Response to comment on "Gender differences in 1,25 dihydroxyvitamin D 3 immunomodulatory effects in multiple sclerosis patients and healthy subjects"

Publicado 2011

Epigenetic modifications in the biology of nonalcoholic fatty liver disease: The role of DNA hydroxymethylation and TET proteins

Publicado 2015

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, Carolina, Nadra, Alejandro Daniel, Taboas, Melisa, Charreau, Eduardo Hernán
Publicado 2011

Somatic Hypermutation Defects in Common Variable Immune Deficiency

Publicado 2017

Failure to Recover from Proactive Semantic Interference and Abnormal Limbic Connectivity in Asymptomatic, Middle-Aged Offspring of Patients with Late-Onset Alzheimer's Disease

Publicado 2017

Histopathology of Sclerotinia sclerotiorum attack on flower parts of Helianthus annuus heads in tolerant and susceptible varieties

por Rodríguez, María Alejandra, Venedikian, Nadia, Bazzalo, María Eugenia, Godeas, Alicia Margarita
Publicado 2004

Reprogramming the body weight set point by a reciprocal interaction of hypothalamic leptin sensitivity and Pomc gene expression reverts extreme obesity

por Rubinstein, Marcelo
Publicado 2016

Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: An international collaborative study

Publicado 2010

Mitochondrial genome architecture in non-alcoholic fatty liver disease

Publicado 2016

The IL-17A rs2275913 single nucleotide polymorphism is associated with protection to tuberculosis but related to higher disease severity in Argentina

por Amiano, Nicolás Oscar, García, Verónica Edith
Publicado 2017

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.
Publicado 2011

Response to comment on "Gender differences in 1,25 dihydroxyvitamin D 3 immunomodulatory effects in multiple sclerosis patients and healthy subjects"

por Correale, J., Ysrraelit, M.C., Gaitán, M.I.

Epigenetic modifications in the biology of nonalcoholic fatty liver disease: The role of DNA hydroxymethylation and TET proteins

por Pirola, C.J., Scian, R., Gianotti, T.F., Dopazo, H., Rohr, C., Martino, J.S., Castaño, G.O., Sookoian, S.

Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: An international collaborative study

por Daly, A.F., Tichomirowa, M.A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M.-L., Barlier, A., Naves, L.A., Ebeling, T., Karhu, A., Raappana, A., Cazabat, L., De Menis, E., Montañana, C.F., Raverot, G., Weil, R.J., Sane, T., Maiter, D., Neggers, S., Yaneva, M., Tabarin, A., Verrua, E., Eloranta, E., Murat, A., Vierimaa, O., Salmela, P.I., Emy, P., Toledo, R.A., Sabaté, M.I., Villa, C., Popelier, M., Salvatori, R., Jennings, J., Longás, Á.F., Aizpún, J.I.L., Georgitsi, M., Paschke, R., Ronchi, C., Valimaki, M., Saloranta, C., De Herder, W., Cozzi, R., Guitelman, M., Magri, F., Lagonigro, M.S., Halaby, G., Corman, V., Hagelstein, M.-T., Vanbellinghen, J.-F., Barra, G.B., Gimenez-Roqueplo, A.-P., Cameron, F.J., Borson-Chazot, F., Holdaway, I., Toledo, S.P.A., Stalla, G.K., Spada, A., Zacharieva, S., Bertherat, J., Brue, T., Bours, V., Chanson, P., Aaltonen, L.A., Beckers, A.

Failure to Recover from Proactive Semantic Interference and Abnormal Limbic Connectivity in Asymptomatic, Middle-Aged Offspring of Patients with Late-Onset Alzheimer's Disease

por Sanchez, S.M., Abulafia, C., Duarte-Abritta, B., De Guevara, M.S.L., Castro, M.N., Drucaroff, L., Sevlever, G., Nemeroff, C.B., Vigo, D.E., Loewenstein, D.A., Villarreal, M.F., Guinjoan, S.M.

Structure-based analysis of five novel disease-causing mutations in 21-hydroxylase-deficient patients

por Minutolo, C., Nadra, A.D., Fernández, C., Taboas, M., Buzzalino, N., Casali, B., Belli, S., Charreau, E.H., Alba, L., Dain, L.

Somatic Hypermutation Defects in Common Variable Immune Deficiency

por Almejun, M.B., Borge, M.

The IL-17A rs2275913 single nucleotide polymorphism is associated with protection to tuberculosis but related to higher disease severity in Argentina

por Rolandelli, A., Del Pino, R.E.H., Pellegrini, J.M., Tateosian, N.L., Amiano, N.O., De La Barrera, S., Casco, N., Gutiérrez, M., Palmero, D.J., García, V.E.

Reprogramming the body weight set point by a reciprocal interaction of hypothalamic leptin sensitivity and Pomc gene expression reverts extreme obesity

por Chhabra, K.H., Adams, J.M., Jones, G.L., Yamashita, M., Schlapschy, M., Skerra, A., Rubinstein, M., Low, M.J.

Mitochondrial genome architecture in non-alcoholic fatty liver disease

por Sookoian, S., Flichman, D., Scian, R., Rohr, C., Dopazo, H., Gianotti, T.F., Martino, J.S., Castaño, G.O., Pirola, C.J.