Intracellular Molecular Differences in Aldosterone- Compared to Cortisol-Secreting Adrenal Cortical Adenomas

por Seidel, Eric, Scholl, Ute I.
Publicado no Front Endocrinol (Lausanne) (2016)

CACNA1H Calcium Channel Mutations in Primary Aldosteronism – Is Sodium the Culprit?

por Stölting, Gabriel, Scholl, Ute I
Publicado no Endocrinology (2020)

Genetic causes of primary aldosteronism

por Seidel, Eric, Schewe, Julia, Scholl, Ute I.
Publicado no Exp Mol Med (2019)

Subcellular localization of fibroblast growth factor receptor type 2 and correlation with CTNNB1 genotype in adrenocortical carcinoma

por Haase, Matthias, Thiel, Anne, Scholl, Ute I., Ashmawy, Hany, Schott, Matthias, Ehlers, Margret
Publicado no BMC Res Notes (2020)

Src-family protein tyrosine kinase phosphorylates WNK4 and modulates its inhibitory effect on KCNJ1 (ROMK)

por Lin, Dao-Hong, Yue, Peng, Yarborough, Orlando, Scholl, Ute I., Giebisch, Gerhard, Lifton, Richard P., Rinehart, Jesse, Wang, Wen-Hui
Publicado no Proc Natl Acad Sci U S A (2015)

KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1)

por Zhang, Chengbiao, Wang, Lijun, Zhang, Junhui, Su, Xiao-Tong, Lin, Dao-Hong, Scholl, Ute I., Giebisch, Gerhard, Lifton, Richard P., Wang, Wen-Hui
Publicado em 2014

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

por Scholl, Ute I., Choi, Murim, Liu, Tiewen, Ramaekers, Vincent T., Häusler, Martin G., Grimmer, Joanne, Tobe, Sheldon W., Farhi, Anita, Nelson-Williams, Carol, Lifton, Richard P.
Publicado em 2009

Macrolides selectively inhibit mutant KCNJ5 potassium channels that cause aldosterone-producing adenoma

por Scholl, Ute I., Abriola, Laura, Zhang, Chengbiao, Reimer, Esther N., Plummer, Mark, Kazmierczak, Barbara I., Zhang, Junhui, Hoyer, Denton, Merkel, Jane S., Wang, Wenhui, Lifton, Richard P.
Publicado no J Clin Invest (2017)

USP8 Mutations in Pituitary Cushing Adenomas—Targeted Analysis by Next-Generation Sequencing

por Ballmann, Cora, Thiel, Anne, Korah, Hannah E, Reis, Anna-Carinna, Saeger, Wolfgang, Stepanow, Stefanie, Köhrer, Karl, Reifenberger, Guido, Knobbe-Thomsen, Christiane B, Knappe, Ulrich J, Scholl, Ute I
Publicado no J Endocr Soc (2018)

Enhanced Ca(2+) signaling, mild primary aldosteronism, and hypertension in a familial hyperaldosteronism mouse model (Cacna1h(M1560V/+))

por Seidel, Eric, Schewe, Julia, Zhang, Junhui, Dinh, Hoang An, Forslund, Sofia K., Markó, Lajos, Hellmig, Nicole, Peters, Jörg, Muller, Dominik N., Lifton, Richard P., Nottoli, Timothy, Stölting, Gabriel, Scholl, Ute I.
Publicado no Proc Natl Acad Sci U S A (2021)

Generation and characterization of a mitotane-resistant adrenocortical cell line

por Seidel, Eric, Walenda, Gudrun, Messerschmidt, Clemens, Obermayer, Benedikt, Peitzsch, Mirko, Wallace, Paal, Bahethi, Rohini, Yoo, Taekyeong, Choi, Murim, Schrade, Petra, Bachmann, Sebastian, Liebisch, Gerhard, Eisenhofer, Graeme, Beule, Dieter, Scholl, Ute I
Publicado no Endocr Connect (2020)

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

por Choi, Murim, Scholl, Ute I., Ji, Weizhen, Liu, Tiewen, Tikhonova, Irina R., Zumbo, Paul, Nayir, Ahmet, Bakkaloğlu, Ayșin, Özen, Seza, Sanjad, Sami, Nelson-Williams, Carol, Farhi, Anita, Mane, Shrikant, Lifton, Richard P.
Publicado em 2009

Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5

por Scholl, Ute I., Nelson-Williams, Carol, Yue, Peng, Grekin, Roger, Wyatt, Robert J., Dillon, Michael J., Couch, Robert, Hammer, Lisa K., Harley, Frances L., Farhi, Anita, Wang, Wen-Hui, Lifton, Richard P.
Publicado em 2012

A novel FOXO1-mediated dedifferentiation blocking role for DKK3 in adrenocortical carcinogenesis

por Cheng, Joyce Y., Brown, Taylor C., Murtha, Timothy D., Stenman, Adam, Juhlin, C. Christofer, Larsson, Catharina, Healy, James M., Prasad, Manju L., Knoefel, Wolfram T., Krieg, Andreas, Scholl, Ute I., Korah, Reju, Carling, Tobias
Publicado no BMC Cancer (2017)

Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

por Goh, Gerald, Scholl, Ute I., Healy, James M., Choi, Murim, Prasad, Manju L., Nelson-Williams, Carol, Kuntsman, John W., Korah, Reju, Suttorp, Anna-Carinna, Dietrich, Dimo, Haase, Matthias, Willenberg, Holger S., Stålberg, Peter, Hellman, Per, Åkerström, Göran, Björklund, Peyman, Carling, Tobias, Lifton, Richard P.
Publicado em 2014

K(+) Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

por Choi, Murim, Scholl, Ute I., Yue, Peng, Björklund, Peyman, Zhao, Bixiao, Nelson-Williams, Carol, Ji, Weizhen, Cho, Yoonsang, Patel, Aniruddh, Men, Clara J., Lolis, Elias, Wisgerhof, Max V., Geller, David S., Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Wang, Wenhui, Carling, Tobias, Lifton, Richard P.
Publicado em 2011

Novel Somatic Mutations in Primary Hyperaldosteronism are related to the Clinical, Radiological and Pathological Phenotype

por Scholl, Ute I., Healy, James M., Thiel, Anne, Fonseca, Annabelle L., Brown, Taylor C., Kunstman, John W., Horne, Matthew J., Dietrich, Dimo, Riemer, Jasmin, Kücükköylü, Seher, Reimer, Esther N., Reis, Anna-Carinna, Goh, Gerald, Kristiansen, Glen, Mahajan, Amit, Korah, Reju, Lifton, Richard P., Prasad, Manju L., Carling, Tobias
Publicado no Clin Endocrinol (Oxf) (2015)

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

por Scholl, Ute I, Stölting, Gabriel, Nelson-Williams, Carol, Vichot, Alfred A, Choi, Murim, Loring, Erin, Prasad, Manju L, Goh, Gerald, Carling, Tobias, Juhlin, C Christofer, Quack, Ivo, Rump, Lars C, Thiel, Anne, Lande, Marc, Frazier, Britney G, Rasoulpour, Majid, Bowlin, David L, Sethna, Christine B, Trachtman, Howard, Fahlke, Christoph, Lifton, Richard P
Publicado no eLife (2015)

Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma

por Juhlin, C. Christofer, Goh, Gerald, Healy, James M., Fonseca, Annabelle L., Scholl, Ute I., Stenman, Adam, Kunstman, John W., Brown, Taylor C., Overton, John D., Mane, Shrikant M., Nelson-Williams, Carol, Bäckdahl, Martin, Suttorp, Anna-Carinna, Haase, Matthias, Choi, Murim, Schlessinger, Joseph, Rimm, David L., Höög, Anders, Prasad, Manju L., Korah, Reju, Larsson, Catharina, Lifton, Richard P., Carling, Tobias
Publicado no J Clin Endocrinol Metab (2015)

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

por Scholl, Ute I., Goh, Gerald, Stölting, Gabriel, de Oliveira, Regina Campos, Choi, Murim, Overton, John D., Fonseca, Annabelle L., Korah, Reju, Starker, Lee F., Kunstman, John W., Prasad, Manju L., Hartung, Erum A., Mauras, Nelly, Benson, Matthew R., Brady, Tammy, Shapiro, Jay R., Loring, Erin, Nelson-Williams, Carol, Libutti, Steven K., Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Björklund, Peyman, Carling, Tobias, Fahlke, Christoph, Hidalgo, Patricia, Lifton, Richard P.
Publicado em 2013