Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer von Park, Jun Hyoung, Vithayathil, Sajna, Kumar, Santosh, Sung, Pi-Lin, Dobrolecki, Lacey Elizabeth, Putluri, Vasanta, Bhat, Vadiraja B., Bhowmik, Salil Kumar, Gupta, Vineet, Arora, Kavisha, Wu, Danli, Tsouko, Efrosini, Zhang, Yiqun, Maity, Suman, Donti, Taraka R., Graham, Brett H., Frigo, Daniel E., Coarfa, Cristian, Yotnda, Patricia, Putluri, Nagireddy, Sreekumar, Arun, Lewis, Michael T., Creighton, Chad J., Wong, Lee-Jun C., Kaipparettu, Benny Abraham

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Clinical and laboratory interpretation of mitochondrial mRNA variants von Wong, Lee‐Jun C., Chen, Ting, Schmitt, Eric S., Wang, Jing, Tang, Sha, Landsverk, Megan, Li, Fangyuan, Zhang, Shulin, Wang, Yue, Zhang, Victor W., Craigen, William J.

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MPV17‐related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects von El‐Hattab, Ayman W., Wang, Julia, Dai, Hongzheng, Almannai, Mohammed, Staufner, Christian, Alfadhel, Majid, Gambello, Michael J., Prasun, Pankaj, Raza, Saleem, Lyons, Hernando J., Afqi, Manal, Saleh, Mohammed A. M., Faqeih, Eissa A., Alzaidan, Hamad I., Alshenqiti, Abduljabbar, Flore, Leigh Anne, Hertecant, Jozef, Sacharow, Stephanie, Barbouth, Deborah S., Murayama, Kei, Shah, Amit A., Lin, Henry C., Wong, Lee‐Jun C.

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Hepatocellular carcinoma associated with tight‐junction protein 2 deficiency von Zhou, Shengmei, Hertel, Paula M., Finegold, Milton J., Wang, Larry, Kerkar, Nanda, Wang, Jing, Wong, Lee‐Jun C., Plon, Sharon E., Sambrotta, Melissa, Foskett, Pierre, Niu, Zhiyv, Thompson, Richard J., Knisely, A.S.

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Crosstalk from non-cancerous mitochondria can inhibit tumor properties of metastatic cells by suppressing oncogenic pathways von Kaipparettu, Benny Abraham, Ma, Yewei, Park, Jun Hyoung, Lee, Tin-Lap, Zhang, Yiqun, Yotnda, Patricia, Creighton, Chad J, Chan, Wai-Yee, Wong, Lee-Jun C

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Next generation molecular diagnosis of mitochondrial disorders von Wong, Lee-Jun C

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ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa von Xu, Mingchu, Eblimit, Aiden, Wang, Jing, Li, Jianli, Wang, Feng, Zhao, Li, Wang, Xia, Xiao, Ningna, Li, Yumei, Wong, Lee-Jun C., Lewis, Richard A., Chen, Rui

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Pathogenic mitochondrial DNA mutations in protein-coding genes von Wong, Lee-Jun C.

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Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing von Qin, Lan, Wang, Jing, Tian, Xia, Yu, Hui, Truong, Cavatina, Mitchell, John J, Wierenga, Klaas J, Craigen, William J, Zhang, Victor Wei, Wong, Lee-Jun C

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Dependable and efficient clinical utility of target capture-based deep sequencing in molecular diagnosis of retinitis pigmentosa von Wang, Jing, Zhang, Victor W, Feng, Yanming, Tian, Xia, Li, Fang-Yuan, Truong, Cavatina, Wang, Guoli, Chiang, Pei-Wen, Lewis, Richard A, Wong, Lee-Jun C

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Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects von Tang, Sha, Wang, Jing, Zhang, Victor Wei, Li, Fang-Yuan, Landsverk, Megan, Cui, Hong, Truong, Cavatina K., Wang, Guoli, Chen, Li Chieh, Graham, Brett, Scaglia, Fernando, Schmitt, Eric S., Craigen, William J., Wong, Lee-Jun C.

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Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States von Miller, Marcus J., Burrage, Lindsay C., Gibson, James B., Strenk, Meghan E., Lose, Edward J., Bick, David P., Elsea, Sarah H., Sutton, V. Reid, Sun, Qin, Graham, Brett H., Craigen, William J., Zhang, Victor Wei, Wong, Lee-Jun C.

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Molecular and clinical genetics of mitochondrial diseases due to POLG mutations von Wong, Lee-Jun C, Naviaux, Robert K, Brunetti-Pierri, Nicola, Zhang, Qing, Schmitt, Eric S, Truong, Cavatina, Milone, Margherita, Cohen, Bruce H, Wical, Beverly, Ganesh, Jaya, Basinger, Alice A, Burton, Barbara K, Swoboda, Kathryn, Gilbert, Donald L, Vanderver, Adeline, Saneto, Russell P, Maranda, Bruno, Arnold, Georgianne, Abdenur, Jose E, Waters, Paula J, Copeland, William C

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Mitochondrial genetic background modifies breast cancer risk von BAI, Ren-Kui, LEAL, Suzanne M, COVARRUBIAS, Daniel, AIYI LIU, WONG, Lee-Jun C

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Mitochondrial Autophagy Promotes Cellular Injury in Nephropathic Cystinosis von SANSANWAL, Poonam, YEN, Benedict, GAHL, William A, YEWEI MA, LIHUA YING, WONG, Lee-Jun C, SARWAL, Minnie M

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Clinical, pathological, imaging, and genetic characterization in a Taiwanese cohort with limb-girdle muscular dystrophy von Liang, Wen-Chen, Jong, Yuh-Jyh, Wang, Chien-Hua, Wang, Chen-Hua, Tian, Xia, Chen, Wan-Zi, Kan, Tzu-Min, Minami, Narihiro, Nishino, Ichizo, Wong, Lee-Jun C.

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Molecular genetics of mitochondrial disorders von Wong, Lee-Jun C.

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The phenotypic variability of HK1-associated retinal dystrophy von Yuan, Zhisheng, Li, Baiyu, Xu, Mingchu, Chang, Emmanuel Y., Li, Huajin, Yang, Lizhu, Wu, Shijing, Soens, Zachry T., Li, Yumei, Wong, Lee-Jun C., Lewis, Richard A., Sui, Ruifang, Chen, Rui

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Correction: Crosstalk from Non-Cancerous Mitochondria Can Inhibit Tumor Properties of Metastatic Cells by Suppressing Oncogenic Pathways von Kaipparettu, Benny Abraham, Ma, Yewei, Park, Jun Hyoung, Lee, Tin-Lap, Zhang, Yiqun, Yotnda, Patricia, Creighton, Chad J, Chan, Wai-Yee, Wong, Lee-Jun C

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POLG DNA testing as an emerging standard of care before instituting valproic acid therapy for pediatric seizure disorders von Saneto, Russell P, Lee, Inn-Chi, Koenig, Mary Kay, Bao, Xinhua, Weng, Shao-Wen, Naviaux, Robert K, Wong, Lee-Jun C

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