Výsledky vyhledávání - Daw‐Yang Hwang

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  1. 1
    Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

    Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans Autor Asaf Vivante, Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Friedhelm Hildebrandt

    Vydáno 2014
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  2. 2
    Deletion of the Noncoding<i>GNAS</i>Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of<i>GNAS</i>Methylation<i>in cis</i>

    Deletion of the Noncoding<i>GNAS</i>Antisense Transcript Causes Pseudohypoparathyroidism Type Ib and Biparental Defects of<i>GNAS</i>Methylation<i>in cis</i> Autor Smitha Chillambhi, Serap Turan, Daw‐Yang Hwang, Hung‐Chun Chen, Harald Jüppner, Murat Bastepe

    Vydáno 2010
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  3. 3
    Genotype, Phenotype, and Follow-Up in Taiwanese Patients with Salt-Losing Tubulopathy Associated with<i>SLC12A3</i>Mutation

    Genotype, Phenotype, and Follow-Up in Taiwanese Patients with Salt-Losing Tubulopathy Associated with<i>SLC12A3</i>Mutation Autor Min‐Hua Tseng, Sung-Sen Yang, Yu‐Juei Hsu, Yu‐Wei Fang, Chih‐Jen Wu, Jeng-Daw Tsai, Daw‐Yang Hwang, Shih‐Hua Lin

    Vydáno 2012
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  4. 4
    Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract

    Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract Autor Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Alina C. Hilger, Pawaree Saisawat, Asaf Vivante, Nataša Stajić, Radovan Bogdanović, Heiko Reutter, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Vydáno 2014
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  5. 5
    Glycated Hemoglobin and Outcomes in Patients with Advanced Diabetic Chronic Kidney Disease

    Glycated Hemoglobin and Outcomes in Patients with Advanced Diabetic Chronic Kidney Disease Autor I‐Ching Kuo, Hugo You‐Hsien Lin, Sheng‐Wen Niu, Daw‐Yang Hwang, Jia‐Jung Lee, Jer‐Chia Tsai, Chi‐Chih Hung, Shang‐Jyh Hwang, Hung‐Chun Chen

    Vydáno 2016
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  6. 6
    Hyponatremia is Associated with Fluid Imbalance and Adverse Renal Outcome in Chronic Kidney Disease Patients Treated with Diuretics

    Hyponatremia is Associated with Fluid Imbalance and Adverse Renal Outcome in Chronic Kidney Disease Patients Treated with Diuretics Autor Lee‐Moay Lim, Ni‐Chin Tsai, Ming‐Yen Lin, Daw‐Yang Hwang, Hugo You‐Hsien Lin, Jia‐Jung Lee, Shang‐Jyh Hwang, Chi‐Chih Hung, Hung‐Chun Chen

    Vydáno 2016
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  7. 7
    Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

    Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract Autor Daw‐Yang Hwang, Gabriel C. Dworschak, Stefan Kohl, Pawaree Saisawat, Asaf Vivante, Alina C. Hilger, Heiko Reutter, Neveen A. Soliman, Radovan Bogdanović, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Vydáno 2014
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  8. 8
    Urinary neutrophil gelatinase‐associated lipocalin levels predict cisplatin‐induced acute kidney injury better than albuminuria or urinary cystatin C levels

    Urinary neutrophil gelatinase‐associated lipocalin levels predict cisplatin‐induced acute kidney injury better than albuminuria or urinary cystatin C levels Autor Hugo You‐Hsien Lin, SC Lee, Sheng‐Fung Lin, Hui‐Hua Hsiao, Yi‐Chang Liu, Wen‐Chi Yang, Daw‐Yang Hwang, Chi‐Chih Hung, Hung‐Chun Chen, Jinn‐Yuh Guh

    Vydáno 2013
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  9. 9
    Hypokalemia, Its Contributing Factors and Renal Outcomes in Patients with Chronic Kidney Disease

    Hypokalemia, Its Contributing Factors and Renal Outcomes in Patients with Chronic Kidney Disease Autor Hsiao-Han Wang, Chi-Chih Hung, Daw‐Yang Hwang, Mei-Chuan Kuo, Yi-Wen Chiu, Jer-Ming Chang, Jer-Chia Tsai, Shang-Jyh Hwang, Julian L. Seifter, Hung‐Chun Chen

    Vydáno 2013
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  10. 10
    Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

    Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract Autor Asaf Vivante, Daw‐Yang Hwang, Stefan Kohl, Jing Chen, Shirlee Shril, Julian Schulz, Amelie van der Ven, Ghaleb H. Daouk, Neveen A. Soliman, Aravind Selvin Kumar, Prabha Senguttuvan, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt

    Vydáno 2016
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  11. 11
    Intercellular TIMP-1-CD63 signaling directs the evolution of immune escape and metastasis in KRAS-mutated pancreatic cancer cells

    Intercellular TIMP-1-CD63 signaling directs the evolution of immune escape and metastasis in KRAS-mutated pancreatic cancer cells Autor Chuan Wang, Ya-Chin Hou, Yi‐Kai Hong, † Y.-H. Tai, Ching-Liang Shen, Pei‐Chi Hou, Jhao-Lin Fu, Cheng-Lin Wu, Siao Muk Cheng, Daw‐Yang Hwang, Yung‐Yeh Su, Yan-Shen Shan, Shaw‐Jenq Tsai

    Vydáno 2025
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  12. 12
    Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association

    Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association Autor Alina C. Hilger, Jan Halbritter, Tracie Pennimpede, Amelie van der Ven, Georgia Sarma, Daniela A. Braun, Jonathan D. Porath, Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Bernhard G. Hermann, Anna Pavlova, Osman El‐Maarri, Markus M. Nöthen, Michael Ludwig, Heiko Reutter, Friedhelm Hildebrandt

    Vydáno 2015
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  13. 13
    ITPKC Single Nucleotide Polymorphism Associated with the Kawasaki Disease in a Taiwanese Population

    ITPKC Single Nucleotide Polymorphism Associated with the Kawasaki Disease in a Taiwanese Population Autor Ho‐Chang Kuo, Kuender D. Yang, Suh‐Hang Hank Juo, Chi‐Di Liang, Wei-Chiao Chen, Yu‐Shiuan Wang, Chih‐Hung Lee, Edward Hsi, Hong‐Ren Yu, Peng-Yeong Woon, I-Chun Lin, Chien-Fu Huang, Daw‐Yang Hwang, Chiu‐Ping Lee, Li-Yan Lin, Wei-Pin Chang, Wei‐Chiao Chang

    Vydáno 2011
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  14. 14
    Macrophage activation determines muscle wasting in pancreatic cancer

    Macrophage activation determines muscle wasting in pancreatic cancer Autor Chih‐Han Chang, Po-Hsien Huang, Szu-Ying Chen, Pei-Chia Su, Li-Yun Ding, Ya‐Chin Hou, Miao‐Neng Hung, Kuan-Lin Chen, Ya‐Na Wu, Shang‐Rung Wu, Forn-Chia Lin, Pei‐Jung Lu, Hsin-Yi Wu, Yu‐Ju Chen, Chih‐Han Chang, Chih‐Peng Chang, Daw-Yang Hwang, Yi‐Ching Wang, Yan‐Shen Shan

    Vydáno 2025
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  15. 15
    Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract

    Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract Autor Daw‐Yang Hwang, Stefan Kohl, Xueping Fan, Asaf Vivante, Stefanie Chan, Gabriel C. Dworschak, Julian Schulz, Albertien M. van Eerde, Alina C. Hilger, Heon Yung Gee, Tracie Pennimpede, Bernhard G. Herrmann, Glenn van de Hoek, Kirsten Y. Renkema, Christoph Schell, Tobias B. Huber, Heiko Reutter, Neveen A. Soliman, Nataša Stajić, Radovan Bogdanović, Elijah O. Kehinde, Richard P. Lifton, Velibor Tasić, Lu W, Friedhelm Hildebrandt

    Vydáno 2015
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  16. 16
    Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

    Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development Autor Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, Stefan Kohl, Amita Sharma, Jing Chen, Shirlee Shril, Daw‐Yang Hwang, Anna-Carina Weiss, Michael M. Kaminski, Rachel Shukrun, Markus J. Kemper, A. Lehnhardt, Rolf Beetz, Simone Sanna‐Cherchi, Miguel Verbitsky, Ali G. Gharavi, Helen M. Stuart, Sally Feather, Judith A. Goodship, Timothy H.J. Goodship, Adrian S. Woolf, Sjirk J. Westra, Daniel P. Doody, Stuart B. Bauer, Richard S. Lee, Rosalyn M. Adam, Lu W, Heiko Reutter, Elijah O. Kehinde, Erika J. Mancini, Richard P. Lifton, Velibor Tasić, Soeren S. Lienkamp, Harald Jüppner, Andreas Kispert, Friedhelm Hildebrandt

    Vydáno 2015
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  17. 17
    Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

    Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association Autor Pawaree Saisawat, Stefan Kohl, Alina C. Hilger, Daw‐Yang Hwang, Heon Yung Gee, Gabriel C. Dworschak, Velibor Tasić, Tracie Pennimpede, S. Natarajan, Ethan D. Sperry, Danilo Swann Matassa, Nataša Stajić, Radovan Bogdanović, Ivo de Blaauw, Carlo Marcelis, Charlotte H. W. Wijers, Enrika Bartels, Eberhard Schmiedeke, Dominik Schmidt, Stefanie Märzheuser, Sabine Grasshoff‐Derr, Stefan Holland‐Cunz, Michael Ludwig, Markus M. Nöthen, Markus Draaken, Erwin Brosens, Hugo A. Heij, Dick Tibboel, Bernhard G. Herrmann, Benjamin D. Solomon, Annelies de Klein, Iris A.L.M. van Rooij, Franca Esposito, Heiko Reutter, Friedhelm Hildebrandt

    Vydáno 2013
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  18. 18
    Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

    Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia Autor Christina Austin‐Tse, Jan Halbritter, Maimoona A. Zariwala, Renée M. Gilberti, Heon Yung Gee, Nathan E. Hellman, Narendra Pathak, Yan Liu, Jennifer R. Panizzi, Ramila S. Patel‐King, Douglas Tritschler, Raqual Bower, Eileen O’Toole, Jonathan D. Porath, Toby W. Hurd, Moumita Chaki, Katrina A. Diaz, Stefan Kohl, Svjetlana Lovric, Daw‐Yang Hwang, Daniela A. Braun, Markus Schueler, Rannar Airik, Edgar A. Otto, Margaret W. Leigh, Peadar G. Noone, Johnny L. Carson, Stephanie D. Davis, Jessica E. Pittman, Thomas W. Ferkol, Jeffrey J. Atkinson, Kenneth N. Olivier, Scott D. Sagel, Sharon Dell, Margaret Rosenfeld, Carlos Milla, Niki T. Loges, Heymut Omran, Mary E. Porter, Stephen M. King, Michael R. Knowles, Iain A. Drummond, Friedhelm Hildebrandt

    Vydáno 2013
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  19. 19
    ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6

    ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6 Autor Maimoona A. Zariwala, Heon Yung Gee, Małgorzata Kurkowiak, Dalal A. Al-Mutairi, Margaret W. Leigh, Toby W. Hurd, Rim Hjeij, Sharon Dell, Moumita Chaki, Gerard W. Dougherty, Mohamed Adan, Philip C. Spear, Julián Esteve-Rudd, Niki T. Loges, Margaret Rosenfeld, Katrina A. Diaz, Heike Olbrich, Whitney Wolf, Eamonn Sheridan, Trevor F.C. Batten, Jan Halbritter, Jonathan D. Porath, Stefan Kohl, Svjetlana Lovric, Daw‐Yang Hwang, Jessica E. Pittman, Kimberlie A. Burns, Thomas W. Ferkol, Scott D. Sagel, Kenneth N. Olivier, Lucy Morgan, Claudius Werner, Johanna Raidt, Petra Pennekamp, Zhaoxia Sun, Weibin Zhou, Rannar Airik, S. Natarajan, Susan J. Allen, Israel Amirav, Dagmar Wieczorek, Kerstin Landwehr, Kim G. Nielsen, Nicolaus Schwerk, Jadranka Sertić, Gabriele Köhler, Joseph Washburn, Shawn Levy, Shuling Fan, Cordula Koerner‐Rettberg, Serge Amselem, David S. Williams, Brian J. Mitchell, Iain A. Drummond, Edgar A. Otto, Heymut Omran, Michael R. Knowles, Friedhelm Hildebrandt

    Vydáno 2013
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  20. 20
    Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract

    Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract Autor Amelie T. van der Ven, Dervla M. Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Jing Chen, Asaf Vivante, Daw‐Yang Hwang, Julian Schulz, Daniela A. Braun, Johanna Magdalena Schmidt, David Schapiro, Ronen Schneider, Jillian K. Warejko, Ankana Daga, Amar J. Majmundar, Weizhen Tan, Tilman Jobst‐Schwan, Tobias Hermle, Eugen Widmeier, Shazia Ashraf, Ali Amar, Charlotte A. Hoogstraaten, Hannah Hugo, Thomas M. Kitzler, Franziska Kause, Caroline M. Kolvenbach, Rufeng Dai, Leslie Spaneas, Kassaundra Amann, Deborah R. Stein, Michelle A. Baum, Michael J.G. Somers, Nancy Rodig, Michael A. Ferguson, Avram Z. Traum, Ghaleb H. Daouk, Radovan Bogdanović, Nataša Stajić, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan Fathy, Danko Milošević, Muna Al‐Saffar, Hazem S. Awad, Loai Eid, Aravind Selvin, Prabha Senguttuvan, Simone Sanna‐Cherchi, Heidi L. Rehm, Daniel G. MacArthur, Monkol Lek, Kristen M. Laricchia, Michael W. Wilson, Shrikant Mane, Richard P. Lifton, Richard S. Lee, Stuart B. Bauer, Lu W, Heiko Reutter, Velibor Tasić, Shirlee Shril, Friedhelm Hildebrandt

    Vydáno 2018
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