Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population

по Jung, Jinsei, Lee, Joon Suk, Cho, Kyeong Jee, Yu, Seyoung, Yoon, Joo-Heon, Yung Gee, Heon, Choi, Jae Young
Опубликовано в: Sci Rep (2017)

Functional characterization of ABCB4 mutations found in progressive familial intrahepatic cholestasis type 3

по Park, Hyo Jin, Kim, Tae Hee, Kim, So Won, Noh, Shin Hye, Cho, Kyeong Jee, Choi, Choe, Kwon, Eun Young, Choi, Yang Ji, Gee, Heon Yung, Choi, Ji Ha
Опубликовано в: Sci Rep (2016)

ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms

по Cho, Kyeong Jee, Noh, Shin Hye, Han, Soo Min, Choi, Won-Il, Kim, Hye-Youn, Yu, Seyoung, Lee, Joon Suk, Rim, John Hoon, Lee, Min Goo, Hildebrandt, Friedhelm, Gee, Heon Yung
Опубликовано в: PLoS Genet (2018)

FAT1 mutations cause a glomerulotubular nephropathy

по Gee, Heon Yung, Sadowski, Carolin E., Aggarwal, Pardeep K., Porath, Jonathan D., Yakulov, Toma A., Schueler, Markus, Lovric, Svjetlana, Ashraf, Shazia, Braun, Daniela A., Halbritter, Jan, Fang, Humphrey, Airik, Rannar, Vega-Warner, Virginia, Cho, Kyeong Jee, Chan, Timothy A., Morris, Luc G. T., ffrench-Constant, Charles, Allen, Nicholas, McNeill, Helen, Büscher, Rainer, Kyrieleis, Henriette, Wallot, Michael, Gaspert, Ariana, Kistler, Thomas, Milford, David V., Saleem, Moin A., Keng, Wee Teik, Alexander, Stephen I., Valentini, Rudolph P., Licht, Christoph, Teh, Jun C., Bogdanovic, Radovan, Koziell, Ania, Bierzynska, Agnieszka, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P., Holzman, Lawrence B., Sibinga, Nicholas E. S., Walz, Gerd, Tufro, Alda, Hildebrandt, Friedhelm
Опубликовано в: Nat Commun (2016)