Interaction effects of temperature and ozone on lung function and markers of systemic inflammation, coagulation, and fibrinolysis: a crossover study of healthy young volunteers von Kahle, Juliette J, Neas, Lucas M, Devlin, Robert B, Case, Martin W, Schmitt, Michael T, Madden, Michael C, Diaz-Sanchez, David

Volltext

MicroRNA Biomarkers of Toxicity in Biological Matrices von Harrill, Alison H, McCullough, Shaun D, Wood, Charles E, Kahle, Juliette J, Chorley, Brian N

Volltext

ATXN1 Protein Family and CIC Regulate Extracellular Matrix Remodeling and Lung Alveolarization von Lee, Yoontae, Fryer, John D., Kang, Hyojin, Crespo-Barreto, Juan, Bowman, Aaron B., Gao, Yan, Kahle, Juliette J., Hong, Jeong Soo, Kheradmand, Farrah, Orr, Harry T., Finegold, Milton J., Zoghbi, Huda Y.

Volltext

Ataxin1L is a regulator of HSC function highlighting the utility of cross-tissue comparisons for gene discovery von Kahle, Juliette J, Souroullas, George P, Yu, Peng, Zohren, Fabian, Lee, Yoontae, Shaw, Chad A, Zoghbi, Huda Y, Goodell, Margaret A

Volltext

Polyglutamine disease toxicity is regulated by Nemo-like kinase in spinocerebellar ataxia type 1 von Ju, Hyoungseok, Kokubu, Hiroshi, Todd, Tiffany W, Kahle, Juliette J, Kim, Soeun, Richman, Ronald, Chirala, Karthik, Orr, Harry T, Zoghbi, Huda Y, Lim, Janghoo

Volltext

Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia von KAHLE, Juliette J, GULBAHCE, Natali, SHAW, Chad A, LIM, Janghoo, HILL, David E, BARABASI, Albert-László, ZOGHBI, Huda Y

Volltext

Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes von Zoghbi, Huda Y, Bowman, Aaron B, Lam, Yung C, Jafar-Nejad, Paymaan, Chen, Hung-Kai, Richman, Ronald, Samaco, Rodney C, Fryer, John D, Kahle, Juliette J, Orr, Harry T

Volltext

Familial segregation of neuropsychiatric phenotypes and a 5’UTR deletion in PTPRD von Kahle, Juliette, Toy, Samantha, Shinawi, Marwan, Cao, Yang

Volltext

eP435 - Familial segregation of neuropsychiatric phenotypes and a 5’UTR deletion in PTPRD von Kahle, Juliette, Toy, Samantha, Shinawi, Marwan, Cao, Yang

Volltext

eP432 - WNT5A haploinsufficiency and gestational diabetes in a newborn with multiple congenital anomalies: a likely gene-environment interaction von Kahle, Juliette, Singh, Prapti, Wein, Alexander, Quirin, Kayla, Cao, Yang, De Luque, Jorge Luis Granadillo

Volltext

WNT5A haploinsufficiency and gestational diabetes in a newborn with multiple congenital anomalies: a likely gene-environment interaction von Kahle, Juliette, Singh, Prapti, Wein, Alexander, Quirin, Kayla, Cao, Yang, De Luque, Jorge Luis Granadillo

Volltext

MicroRNA Biomarkers of Toxicity in Biological Matrices von Harrill, Alison H., McCullough, Shaun D., Wood, Charles E., Kahle, Juliette J., Chorley, Brian N.

Volltext

21. Co-existence of two activating variants in somatic overgrowth & vascular anomalies: 7 years' findings at a single center von Cao, Yang, Bell, Robert, Evenson, Michael, Corliss, Meagan, Kahle, Juliette, Saadalla, Abdulrahman, Schroeder, Molly, Krysiak, Kilannin, Amarillo, Ina, Heusel, Jonathan, Neidich, Julie

Volltext

Further delineation of the SCAF4-associated neurodevelopmental disorder von Schmid, Cosima M, Gregor, Anne, Ruiz, Anna, Manso Bazús, Carmen, Herman, Isabella, Ammouri, Farah, Kotzaeridou, Urania, McNiven, Vanda, Dupuis, Lucie, Steindl, Katharina, Begemann, Anaïs, Rauch, Anita, Suter, Aude-Annick, Isidor, Bertrand, Mercier, Sandra, Nizon, Mathilde, Cogné, Benjamin, Deb, Wallid, Besnard, Thomas, Haack, Tobias B, Falb, Ruth J, Müller, Amelie J, Linden, Tobias, Haldeman-Englert, Chad R, Ockeloen, Charlotte W, Mattioli, Francesca, Reymond, Alexandre, Ibrahim, Nazia, Naz, Shagufta, Lacaze, Elodie, Bassetti, Jennifer A, Hoefele, Julia, Brunet, Theresa, Riedhammer, Korbinian M, Elloumi, Houda Z, Person, Richard, Zou, Fanggeng, Kahle, Juliette J, Cremer, Kirsten, Schmidt, Axel, Delrue, Marie-Ange, Almeida, Pedro M, Ramos, Fabiana, Srivastava, Siddharth, Quinlan, Aisling, Robertson, Stephen, Manka, Eva, Kuechler, Alma, Spranger, Stephanie, Nowaczyk, Malgorzata J M, Elshafie, Reem M, Alsharhan, Hind, Hillman, Paul R, Dunnington, Leslie A, Braakman, Hilde M H, McKee, Shane, Moresco, Angelica, Ignat, Andrea-Diana, Newbury-Ecob, Ruth, Banneau, Guillaume, Patat, Olivier, Kuerbitz, Jeffrey, Rzucidlo, Susan, Sell, Susan S, Gordon, Patricia, Schuhmann, Sarah, Reis, André, Halleb, Yosra, Stoeva, Radka, Keren, Boris, Al Masseri, Zainab, Tümer, Zeynep, Hammer-Hansen, Sophia, Krüger Sølyst, Sofus, Steigerwald, Connolly G, Abreu, Nicolas J, Faust, Helene, Müller-Nedebock, Amica, Tran Mau-Them, Frédéric, Sticht, Heinrich, Zweier, Christiane

Volltext

Ataxin1L Is a Regulator of HSC Function Highlighting the Utility of Cross-Tissue Comparisons for Gene Discovery: e1003359 von Kahle, Juliette J, Souroullas, George P, Yu, Peng, Zohren, Fabian, Lee, Yoontae, Shaw, Chad A, Zoghbi, Huda Y, Goodell, Margaret A

Volltext