Modulation of Tight Junction Structure and Function by Kinases and Phosphatases Targeting Occludin

por Dörfel, Max Johannes, Huber, Otmar
Publicado 2012

Proteomic and genomic characterization of a yeast model for Ogden syndrome

por Dörfel, Max J., Fang, Han, Crain, Jonathan, Klingener, Michael, Weiser, Jake, Lyon, Gholson J.
Publicado 2016

Three Cases of Alcohol-Induced Acute-On-Chronic Liver Failure With Successful Support by Adipose-Derived Stem Cells

por Götze, Tobias, Krueger, Michael, Meutsch, Juliane, Dörfel, Max, Born, Stephan, Sowa, Jan-Peter, Canbay, Ali
Publicado 2019

CK2-dependent phosphorylation of occludin regulates the interaction with ZO-proteins and tight junction integrity

por Dörfel, Max J, Westphal, Julie K, Bellmann, Christian, Krug, Susanne M, Cording, Jimmi, Mittag, Sonnhild, Tauber, Rudolf, Fromm, Michael, Blasig, Ingolf E, Huber, Otmar
Publicado 2013

Evaluating possible maternal effect lethality of Naa10 knockout mice, and modulation of phenotypes for embryonic and neonatal lethality by genetic background and environment

por Lyon, Gholson J., Longo, Joseph, Garcia, Andrew, Inusa, Fatima, Marchi, Elaine, Shi, Daniel, Dörfel, Max, Arnesen, Thomas, Aldabe, Rafael, Lyons, Scott, Nashat, Melissa, Bolton, David
Publicado 2023

A short-term plastic adherence incubation of the stromal vascular fraction leads to a predictable GMP-compliant cell-product

por Born, Stephan, Dörfel, Max Johannes, Hartjen, Philip, Haschemi Yekani, Seyed Ali, Luecke, Julia, Meutsch, Juliane Katharina, Westphal, Julie Katharina, Birkelbach, Moritz, Köhnke, Robert, Smeets, Ralf, Krueger, Michael
Publicado 2019

Biochemical and cellular analysis of Ogden syndrome reveals downstream Nt-acetylation defects

por Myklebust, Line M., Van Damme, Petra, Støve, Svein I., Dörfel, Max J., Abboud, Angèle, Kalvik, Thomas V., Grauffel, Cedric, Jonckheere, Veronique, Wu, Yiyang, Swensen, Jeffrey, Kaasa, Hanna, Liszczak, Glen, Marmorstein, Ronen, Reuter, Nathalie, Lyon, Gholson J., Gevaert, Kris, Arnesen, Thomas
Publicado 2015

Naa12 compensates for Naa10 in mice in the amino-terminal acetylation pathway

por Kweon, Hyae Yon, Lee, Mi-Ni, Dorfel, Max, Seo, Seungwoon, Gottlieb, Leah, PaPazyan, Thomas, McTiernan, Nina, Ree, Rasmus, Bolton, David, Garcia, Andrew, Flory, Michael, Crain, Jonathan, Sebold, Alison, Lyons, Scott, Ismail, Ahmed, Marchi, Elaine, Sonn, Seong-keun, Jeong, Se-Jin, Jeon, Sejin, Ju, Shinyeong, Conway, Simon J, Kim, Taesoo, Kim, Hyun-Seok, Lee, Cheolju, Roh, Tae-Young, Arnesen, Thomas, Marmorstein, Ronen, Oh, Goo Taeg, Lyon, Gholson J
Publicado 2021

TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations

por O’Rawe, Jason A., Wu, Yiyang, Dörfel, Max J., Rope, Alan F., Au, P.Y. Billie, Parboosingh, Jillian S., Moon, Sungjin, Kousi, Maria, Kosma, Konstantina, Smith, Christopher S., Tzetis, Maria, Schuette, Jane L., Hufnagel, Robert B., Prada, Carlos E., Martinez, Francisco, Orellana, Carmen, Crain, Jonathan, Caro-Llopis, Alfonso, Oltra, Silvestre, Monfort, Sandra, Jiménez-Barrón, Laura T., Swensen, Jeffrey, Ellingwood, Sara, Smith, Rosemarie, Fang, Han, Ospina, Sandra, Stegmann, Sander, Den Hollander, Nicolette, Mittelman, David, Highnam, Gareth, Robison, Reid, Yang, Edward, Faivre, Laurence, Roubertie, Agathe, Rivière, Jean-Baptiste, Monaghan, Kristin G., Wang, Kai, Davis, Erica E., Katsanis, Nicholas, Kalscheuer, Vera M., Wang, Edith H., Metcalfe, Kay, Kleefstra, Tjitske, Innes, A. Micheil, Kitsiou-Tzeli, Sophia, Rosello, Monica, Keegan, Catherine E., Lyon, Gholson J.
Publicado 2015