Resultados de búsqueda - Lee, Hwei-Jen

The effect of N-terminal truncation on double-dimer assembly of goose δ-crystallin por Lee, Hwei-Jen, Lai, Young-Hsang, Wu, Su-Ying, Chen, Yu-Hou

Enlace del recurso Enlace del recurso Enlace del recurso

Kinetic Refolding Barrier of Guanidinium Chloride Denatured Goose δ-Crystallin Leads to Regular Aggregate Formation por Yin, Fon-Yi, Chen, Ya-Huei, Yu, Chung-Ming, Pon, Yu-Chin, Lee, Hwei-Jen

Enlace del recurso Enlace del recurso Enlace del recurso

The interaction of Glu294 at the subunit interface is important for the activity and stability of goose δ-crystallin por Huang, Chih-Wei, Chen, Yu-Hou, Chen, Ya-Huei, Tsai, Yun-Chi, Lee, Hwei-Jen

Enlace del recurso Enlace del recurso

The Catalytic Roles of P185 and T188 and Substrate-Binding Loop Flexibility in 3α-Hydroxysteroid Dehydrogenase/Carbonyl Reductase from Comamonas testosteroni por Hwang, Chi-Ching, Chang, Yi-Hsun, Lee, Hwei-Jen, Wang, Tzu-Pin, Su, Yu-Mei, Chen, Hsin-Wei, Liang, Po-Huang

Enlace del recurso Enlace del recurso Enlace del recurso

The Interactions in the Carboxyl Terminus of Human 4-Hydroxyphenylpyruvate Dioxygenase Are Critical to Mediate the Conformation of the Final Helix and the Tail to Shield the Active... por Lin, Jang-Foung, Sheih, Yung-Lin, Chang, Tsu-Chung, Chang, Ni-Yuan, Chang, Chiung-Wen, Shen, Chia-Pei, Lee, Hwei-Jen

Enlace del recurso Enlace del recurso Enlace del recurso

Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia por Tseng, Min-Hua, Huang, Shih-Ming, Lo, Fu-Sung, Huang, Jing-Long, Cheng, Chih-Jen, Lee, Hwei-Jen, Lin, Shih-Hua

Enlace del recurso Enlace del recurso Enlace del recurso

Whole Exome Sequencing Identifies a Novel Homozygous Missense Mutation in the CSB Protein-Encoding ERCC6 Gene in a Taiwanese Boy with Cockayne Syndrome por Lin, Ching-Ming, Yang, Jay-How, Lee, Hwei-Jen, Lin, Yu-Pang, Tsai, Li-Ping, Hsu, Chih-Sin, Luxton, G. W. Gant, Hu, Chih-Fen

Enlace del recurso Enlace del recurso Enlace del recurso

Complement Factor I Mutation May Contribute to Development of Thrombotic Microangiopathy in Lupus Nephritis por Tseng, Min-Hua, Fan, Wen-Lang, Liu, Hsuan, Yang, Chia-Yu, Ding, Jhao-Jhuang, Lee, Hwei-Jen, Huang, Shih-Ming, Lin, Shih-Hua, Huang, Jing-Long

Enlace del recurso Enlace del recurso Enlace del recurso

Autosomal Recessive Renal Tubular Dysgenesis Caused by a Founder Mutation of Angiotensinogen por Tseng, Min-Hua, Huang, Shih-Ming, Huang, Jing-Long, Fan, Wen-Lang, Konrad, Martin, Shaw, Steven W., Lien, Reyin, Chien, Hui-Ping, Ding, Jhao-Jhuang, Wu, Tai-Wei, Tsai, Jeng-Daw, Tian, Ya-Chung, Lee, Hwei-Jen, Cheng, Po-Jen, Hsu, Jen-Fu, Lin, Shih-Hua

Enlace del recurso Enlace del recurso Enlace del recurso

Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia por Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Dündar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Catala Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita, Houlden, Henry, Bartesaghi, Luca, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark, Senderek, Jan

Enlace del recurso Enlace del recurso Enlace del recurso

Erratum to: Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia por Wiessner, Manuela, Maroofian, Reza, Ni, Meng-Yuan, Pedroni, Andrea, Müller, Juliane S, Stucka, Rolf, Beetz, Christian, Efthymiou, Stephanie, Santorelli, Filippo M, Alfares, Ahmed A, Zhu, Changlian, Uhrova Meszarosova, Anna, Alehabib, Elham, Bakhtiari, Somayeh, Janecke, Andreas R, Otero, Maria Gabriela, Chen, Jin Yun Helen, Peterson, James T, Strom, Tim M, De Jonghe, Peter, Deconinck, Tine, De Ridder, Willem, De Winter, Jonathan, Pasquariello, Rossella, Ricca, Ivana, Alfadhel, Majid, van de Warrenburg, Bart P, Portier, Ruben, Bergmann, Carsten, Ghasemi Firouzabadi, Saghar, Jin, Sheng Chih, Bilguvar, Kaya, Hamed, Sherifa, Abdelhameed, Mohammed, Haridy, Nourelhoda A, Maqbool, Shazia, Rahman, Fatima, Anwar, Najwa, Carmichael, Jenny, Pagnamenta, Alistair T, Wood, Nick W, Tran Mau-Them, Frederic, Haack, Tobias, Di Rocco, Maja, Ceccherini, Isabella, Iacomino, Michele, Zara, Federico, Salpietro, Vincenzo, Scala, Marcello, Rusmini, Marta, Xu, Yiran, Wang, Yinghong, Suzuki, Yasuhiro, Koh, Kishin, Nan, Haitian, Ishiura, Hiroyuki, Tsuji, Shoji, Lambert, Laëtitia, Schmitt, Emmanuelle, Lacaze, Elodie, Küpper, Hanna, Dredge, David, Skraban, Cara, Goldstein, Amy, Willis, Mary J H, Grand, Katheryn, Graham, John M, Lewis, Richard A, Millan, Francisca, Duman, Özgür, Olgac Dundar, Nihal, Uyanik, Gökhan, Schöls, Ludger, Nürnberg, Peter, Nürnberg, Gudrun, Català-Bordes, Andrea, Seeman, Pavel, Kuchar, Martin, Darvish, Hossein, Rebelo, Adriana, Bouçanova, Filipa, Medard, Jean-Jacques, Chrast, Roman, Auer-Grumbach, Michaela, Alkuraya, Fowzan S, Shamseldin, Hanan, Al Tala, Saeed, Rezazadeh Varaghchi, Jamileh, Najafi, Maryam, Deschner, Selina, Gläser, Dieter, Hüttel, Wolfgang, Kruer, Michael C, Kamsteeg, Erik-Jan, Takiyama, Yoshihisa, Züchner, Stephan, Baets, Jonathan, Synofzik, Matthis, Schüle, Rebecca, Horvath, Rita, Houlden, Henry, Bartesaghi, Luca, Lee, Hwei-Jen, Ampatzis, Konstantinos, Pierson, Tyler Mark, Senderek, Jan

Enlace del recurso Enlace del recurso Enlace del recurso