Double SET point: G9a makes its mark in adipogenesis

nork Cristancho, Ana G, Lazar, Mitchell A
Argitaratua 2013

Forming functional fat: a growing understanding of adipocyte differentiation

nork Cristancho, Ana G., Lazar, Mitchell A.
Argitaratua izan da Nat Rev Mol Cell Biol (2011)

Epigenetics modifiers: potential hub for understanding and treating neurodevelopmental disorders from hypoxic injury

nork Cristancho, Ana G., Marsh, Eric D.
Argitaratua izan da J Neurodev Disord (2020)

A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A

nork Tian, Guoling, Cristancho, Ana G., Dubbs, Holly A., Liu, Grant T., Cowan, Nicholas J., Goldberg, Ethan M.
Argitaratua izan da Mol Genet Genomic Med (2016)

Repressor transcription factor 7-like 1 promotes adipogenic competency in precursor cells

nork Cristancho, Ana G., Schupp, Michael, Lefterova, Martina I., Cao, Shengya, Cohen, Daniel M., Chen, Christopher S., Steger, David J., Lazar, Mitchell A.
Argitaratua 2011

An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes

nork Yardeni, Tal, Cristancho, Ana G., McCoy, Almedia J., Schaefer, Patrick M., McManus, Meagan J., Marsh, Eric D., Wallace, Douglas C.
Argitaratua izan da Proc Natl Acad Sci U S A (2021)

Stereospecificity of Retinol Saturase: Absolute Configuration, Synthesis, and Biological Evaluation of Dihydroretinoids

nork Moise, Alexander R., Domínguez, Marta, Alvarez, Susana, Alvarez, Rosana, Schupp, Michael, Cristancho, Ana G., Kiser, Philip D., de Lera, Angel R., Lazar, Mitchell A., Palczewski, Krzysztof
Argitaratua 2008

Postnatal Arx transcriptional activity regulates functional properties of PV interneurons

nork Joseph, Donald J., Von Deimling, Markus, Hasegawa, Yuiko, Cristancho, Ana G., Ahrens-Nicklas, Rebecca C., Rogers, Stephanie L., Risbud, Rashmi, McCoy, Almedia J., Marsh, Eric D.
Argitaratua izan da iScience (2020)

Re-expression of GATA2 Cooperates with Peroxisome Proliferator-activated Receptor-γ Depletion to Revert the Adipocyte Phenotype

nork Schupp, Michael, Cristancho, Ana G., Lefterova, Martina I., Hanniman, Elyisha A., Briggs, Erika R., Steger, David J., Qatanani, Mohammed, Curtin, Joshua C., Schug, Jonathan, Ochsner, Scott A., McKenna, Neil J., Lazar, Mitchell A.
Argitaratua 2009

Retinol saturase promotes adipogenesis and is downregulated in obesity

nork Schupp, Michael, Lefterova, Martina I., Janke, Jürgen, Leitner, Kirstin, Cristancho, Ana G., Mullican, Shannon E., Qatanani, Mohammed, Szwergold, Nava, Steger, David J., Curtin, Joshua C., Kim, Roy J., Suh, Moo-jin, Albert, Martin R., Engeli, Stefan, Gudas, Lorraine J., Lazar, Mitchell A.
Argitaratua 2009

IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

nork Mignot, Cyril, McMahon, Aoife C., Bar, Claire, Campeau, Philippe M, Davidson, Claire, Buratti, Julien, Nava, Caroline, Jacquemont, Marie-Line, Tallot, Marilyn, Milh, Mathieu, Edery, Patrick, Marzin, Pauline, Barcia, Giulia, Barnerias, Christine, Besmond, Claude, Bienvenu, Thierry, Bruel, Ange-Line, Brunga, Ledia, Ceulemans, Berten, Coubes, Christine, Cristancho, Ana G., Cunningham, Fiona, Dehouck, Marie-Bertille, Donner, Elizabeth J., Duban-Bedu, Bénédicte, Dubourg, Christèle, Gardella, Elena, Gauthier, Julie, Geneviève, David, Gobin-Limballe, Stéphanie, Goldberg, Ethan M., Hagebeuk, Eveline, Hamdan, Fadi F., Hančárová, Miroslava, Hubert, Laurence, Ioos, Christine, Ichikawa, Shoji, Janssens, Sandra, Journel, Hubert, Kaminska, Anna, Keren, Boris, Koopmans, Marije, Lacoste, Caroline, Laššuthová, Petra, Lederer, Damien, Lehalle, Daphné, Marjanovic, Dragan, Métreau, Julia, Michaud, Jacques L., Miller, Kathryn, Minassian, Berge A., Morales, Joannella, Moutard, Marie-Laure, Munnich, Arnold, Ortiz-Gonzalez, Xilma R., Pinard, Jean-Marc, Prchalová, Darina, Putoux, Audrey, Quelin, Chloé, Rosen, Alyssa R., Roume, Joelle, Rossignol, Elsa, Simon, Marleen E. H., Smol, Thomas, Shur, Natasha, Shelihan, Ivan, Štěrbová, Katalin, Vyhnálková, Emílie, Vilain, Catheline, Soblet, Julie, Smits, Guillaume, Yang, Samuel P., van der Smagt, Jasper J., van Hasselt, Peter M., van Kempen, Marjan, Weckhuysen, Sarah, Helbig, Ingo, Villard, Laurent, Héron, Delphine, Koeleman, Bobby, Møller, Rikke S., Lesca, Gaetan, Helbig, Katherine L., Nabbout, Rima, Verbeek, Nienke E., Depienne, Christel
Argitaratua izan da Genet Med (2018)

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

nork Mignot, Cyril, McMahon, Aoife C., Bar, Claire, Campeau, Philippe M., Davidson, Claire, Buratti, Julien, Nava, Caroline, Jacquemont, Marie-Line, Tallot, Marilyn, Milh, Mathieu, Edery, Patrick, Marzin, Pauline, Barcia, Giulia, Barnerias, Christine, Besmond, Claude, Bienvenu, Thierry, Bruel, Ange-Line, Brunga, Ledia, Ceulemans, Berten, Coubes, Christine, Cristancho, Ana G., Cunningham, Fiona, Dehouck, Marie-Bertille, Donner, Elizabeth J., Duban-Bedu, Bénédicte, Dubourg, Christèle, Gardella, Elena, Gauthier, Julie, Geneviève, David, Gobin-Limballe, Stéphanie, Goldberg, Ethan M., Hagebeuk, Eveline, Hamdan, Fadi F., Hančárová, Miroslava, Hubert, Laurence, Ioos, Christine, Ichikawa, Shoji, Janssens, Sandra, Journel, Hubert, Kaminska, Anna, Keren, Boris, Koopmans, Marije, Lacoste, Caroline, Laššuthová, Petra, Lederer, Damien, Lehalle, Daphné, Marjanovic, Dragan, Métreau, Julia, Michaud, Jacques L., Miller, Kathryn, Minassian, Berge A., Morales, Joannella, Moutard, Marie-Laure, Munnich, Arnold, Ortiz-Gonzalez, Xilma R., Pinard, Jean-Marc, Prchalová, Darina, Putoux, Audrey, Quelin, Chloé, Rosen, Alyssa R., Roume, Joelle, Rossignol, Elsa, Simon, Marleen E. H., Smol, Thomas, Shur, Natasha, Shelihan, Ivan, Štěrbová, Katalin, Vyhnálková, Emílie, Vilain, Catheline, Soblet, Julie, Smits, Guillaume, Yang, Samuel P., van der Smagt, Jasper J., van Hasselt, Peter M., van Kempen, Marjan, Weckhuysen, Sarah, Helbig, Ingo, Villard, Laurent, Héron, Delphine, Koeleman, Bobby, Møller, Rikke S., Lesca, Gaetan, Helbig, Katherine L., Nabbout, Rima, Verbeek, Nienke E., Depienne, Christel
Argitaratua izan da Genet Med (2018)