Gouon-Evans Lab - Publications



Goldman, O*, S. Han*, W. Hamou, V. Jodon de Villeroche, G. Uzan, H. Lickert, V. Gouon-Evans (2014). Endoderm generates endothelial cells during liver development. Stem Cell Reports, 3, 556-565. Press Release: Read

Gouon-Evans V. (2014). The Race for Regeneration: Pluripotent-Stem-Cell-Derived 3D Kidney Structures. Cell Stem Cell, In Press.

Goldman O*, Han S*, Gouon-Evans V. (2014). Liver progenitor cell and KDR. Cell Cycle, 13,7:1051-1052. Selected for the cover page.


Marion Sourisseau, M.*, Goldman, O.*, He, W., Gori, J. L., Kiem, H., Gouon-Evans, V.,** Evans, M.J.** (2013). Pigtail macaque induced pluripotent stem cell-derived hepatocytes support hepatitis C virus infection. Gastroenterology. 145:5,966-969 e7. In “Mount Sinai in the News”. Press Release: Read

Goldman, O.*, S. Han*, M. Sourrisseau, N. Dziedzic, W. Hamou, B. Corneo, S. D'Souza, T. Sato, D.N. Kotton, K.D. Bissig, T. Kalir, A. Jacobs, T. Evans, M.J. Evans, and V. Gouon-Evans. (2013). KDR Identifies a Conserved Human and Murine Hepatic Progenitor and Instructs Early Liver Development. Cell Stem Cell. 12:748-760. PMID: 23746980. In “Mount Sinai in the News”.  Press Release: Read


Han, S., Bourdon, A., Hamou, W., Dziedzic, N., Goldman, O., and Gouon-Evans, V. (2012). Generation of functional hepatic cells from pluripotent stem cells. Journal of Stem Cell Research & Therapy, S10-008.

Cashman, T.J., Gouon-Evans, V, and Costa, K.D. (2012). Mesenchymal Stem Cells for Cardiac Therapy: Practical Challenges and Potential Mechanisms. Stem Cell Rev and Rep, online.


Kubo, A., Stull. R., Takeuchi, M., Bonham, K., Gouon-Evans, V., Sho, M., Iwano, M., Saito, Y., Keller, G., and Snodgrass, R. (2011). Pdx1 and Ngn3 overexpression enhances pancreatic differentiation of mouse ES cell-derived endoderm population. PLoS One, 6, e24058.

Christodoulou C, Longmire T, Shen S, Bourdon A, Sommer  C, Gadue P,  Spira A, Gouon-Evans V, Murphy G, Mostoslavsky G, and Kotton D. (2011). Induced pluripotent stem cells and embryonic stem cells display similar capacity to form definitive endoderm despite molecular differences in imprinted genes. J Clin Invest. 121, 2313-25.

Green, M., Chen, A., Nostro, MC, d’Souza, S., Schaniel, C., Lemischka, I.R., Gouon-Evans, V., Keller, G., Snoeck, H. (2011). Generation of anterior foregut endoderm from human embryonic and induced pluripotent stem cells. Nat Biotechnol, 29, 267-72.

Han, S., Dziedzic, N., Gadue, P., Keller, G., Gouon-Evans V. (2011). An endothelial cell niche induces hepatic specification through dual repression of Wnt and Notch Signaling. Stem Cells, 29, 217-28.


Zhao, X., Monson, C., Gao, C., Gouon-Evans, V., Matsumoto, N., Sadler-Edelpi, K., and Friedman, S. L. (2010). Klf6/copeb is required for hepatic outgrowth in zebrafish and for hepatocyte specification in mouse ES cells. Dev Biol, 344, 79-93.


Gadue, P., Gouon-Evans, V., Cheng, X., Wandzioch, E., Zaret, K.S., Grompe, M., Streeter, P. R., and Keller, G. M. (2009). The Generation of Monoclonal Antibodies Specific for Cell Surface Molecules Expressed on Early Mouse Endoderm. Stem Cells, 1066-5099.


Gouon-Evans, V., Boussemart, L., Gadue, P., Nierhoff, D., Koehler, C. I., Kubo, A., Shafritz, D. A., and Keller, G. (2006). BMP-4 is required for hepatic specification of mouse embryonic stem cell-derived definitive endoderm. Nat Biotechnol 24, 1402-1411.

Ingman, W. V., Wyckoff, J., Gouon-Evans, V., Condeelis, J., and Pollard, J. W. (2006). Macrophages promote collagen fibrillogenesis around terminal end buds of the developing mammary gland. Dev Dyn 235, 3222-3229.


Banaei-Bouchareb, L., Gouon-Evans, V., Samara-Boustani, D., Castellotti, M. C., Czernichow, P., Pollard, J. W., and Polak, M. (2004). Insulin cell mass is altered in Csf1op/Csf1op macrophage-deficient mice. J Leukoc Biol 76, 359-367.


Iyengar, P., Combs, T. P., Shah, S. J., Gouon-Evans, V., Pollard, J. W., Albanese, C., Flanagan, L., Tenniswood, M. P., Guha, C., Lisanti, M. P., et al. (2003). Adipocyte-secreted factors synergistically promote mammary tumorigenesis through induction of anti-apoptotic transcriptional programs and proto-oncogene stabilization. Oncogene 22, 6408-6423.


Lin, E. Y., Gouon-Evans, V., Nguyen, A. V., and Pollard, J. W. (2002). The macrophage growth factor CSF-1 in mammary gland development and tumor progression. J Mammary Gland Biol Neoplasia 7, 147-162.

Gouon-Evans, V., Lin, E. Y., and Pollard, J. W. (2002). Requirement of macrophages and eosinophils and their cytokines/chemokines for mammary gland development. Breast Cancer Res 4, 155-164.

Gouon-Evans, V., and Pollard, J. W. (2002). Unexpected deposition of brown fat in mammary gland during postnatal development. Mol Endocrinol 16, 2618-2627.


Gouon-Evans, V., and Pollard, J. W. (2001). Eotaxin is required for eosinophil homing into the stroma of the pubertal and cycling uterus. Endocrinology 142, 4515-4521.


Gouon-Evans, V., Rothenberg, M. E., and Pollard, J. W. (2000). Postnatal mammary gland development requires macrophages and eosinophils. Development 127, 2269-2282.


Janji, B., Melchior, C., Gouon, V., Vallar, L., and Kieffer, N. (1999). Autocrine TGF-beta-regulated expression of adhesion receptors and integrin-linked kinase in HT-144 melanoma cells correlates with their metastatic phenotype. Int J Cancer 83, 255-262.


Schaffner-Reckinger, E., Gouon, V., Melchior, C., Plancon, S., and Kieffer, N. (1998). Distinct involvement of beta3 integrin cytoplasmic domain tyrosine residues 747 and 759 in integrin-mediated cytoskeletal assembly and phosphotyrosine signaling. J Biol Chem 273, 12623-12632.


Kieffer, N., Melchior, C., Guinet, J. M., Michels, S., Gouon, V., and Bron, N. (1996). Serine 752 in the cytoplasmic domain of the beta 3 integrin subunit is not required for alpha v beta 3 postreceptor signaling events. Cell Adhes Commun 4, 25-39.

Gouon, V., Tucker, G. C., Kraus-Berthier, L., Atassi, G., and Kieffer, N. (1996). Up-regulated expression of the beta3 integrin and the 92-kDa gelatinase in human HT-144 melanoma cell tumors grown in nude mice. Int J Cancer 68, 650-662.

Authors contributed equally, ** co-corresponding authors.