Serum Leptin Level Is a Regulator of Bone Mass von Elefteriou, F., Takeda, S., Ebihara, K., Magre, J., Patano, N., Kim, C. Ae, Ogawa, Y., Liu, X., Ware, S. M., Craigen, W. J., Robert, J. J., Vinson, C., Nakao, K., Capeau, J., Karsenty, G., Chambon, Pierre

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Requirement of voltage-dependent anion channel 2 for pro-apoptotic activity of Bax von Yamagata, H, Shimizu, S, Nishida, Y, Watanabe, Y, Craigen, W J, Tsujimoto, Y

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FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome von Dai, H., Zhang, V.W., El‐Hattab, A.W., Ficicioglu, C., Shinawi, M., Lines, M., Schulze, A., McNutt, M., Gotway, G., Tian, X., Chen, S., Wang, J., Craigen, W.J., Wong, L.‐J.

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Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes von Ware, S M, El-Hassan, N, Kahler, S G, Zhang, Q, Y-W, Miller, E, Wong, B, Spicer, R L, Craigen, W J, Kozel, B A, Grange, D K, Wong, L-J

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VDAC2 Inhibits BAK Activation and Mitochondrial Apoptosis von Emily H. -Y. Cheng, Sheiko, Tatiana V., Fisher, Jill K., Craigen, William J., Korsmeyer, Stanley J.

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Expanding the phenotype of SLC25A42‐associated mitochondrial encephalomyopathy von Almannai, M., Alasmari, A., Alqasmi, A., Faqeih, E., Al Mutairi, F., Alotaibi, M., Samman, M.M., Eyaid, W., Aljadhai, Y.I., Shamseldin, H.E., Craigen, W., Alkuraya, F.S.

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Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase von Dimmock, D.P, Zhang, Q, Dionisi-Vici, C, Carrozzo, R, Shieh, J, Tang, L.Y, Truong, C, Schmitt, E, Sifry-Platt, M, Lucioli, S, Santorelli, F.M, Ficicioglu, C.H, Rodriguez, M, Wierenga, K, Enns, G.M, Longo, N, Lipson, M.H, Vallance, H, Craigen, W.J, Scaglia, F, Wong, L.J

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Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy von PIGNATELLI, Ricardo H, MCMAHON, Colin J, CLUNIE, Sarah, FERNBACH, Susan, BOWLES, Neil E, TOWBIN, Jeffrey A, DREYER, William J, DENFIELD, Susan W, PRICE, Jack, BELMONT, John W, CRAIGEN, William J, JEN WU, HOWAIDA EL SAID, BEZOLD, Louis I

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Mutations in the DNAH11 (Axonemal Heavy Chain Dynein type 11) Gene Cause One Form of Situs Inversus Totalis and Most Likely Primary Ciliary Dyskinesia von Bartoloni, Lucia, Blouin, Jean-Louis, Pan, Yanzhen, Gehrig, Corinne, Maiti, Amit K., Scamuffa, Nathalie, Rossier, Colette, Jorissen, Mark, Armengot, Miguel, Meeks, Maggie, Mitchison, Hannah M., Eddie M. K. Chung, Delozier-Blanchet, Celia D., Craigen, William J., Antonarakis, Stylianos E.

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Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria von Struys, Eduard A., Salomons, Gajja S., Achouri, Younes, Van Schaftingen, Emile, Grosso, Salvatore, Craigen, William J., Verhoeven, Nanda M., Jakobs, Cornelis

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Immotile Sperm and Infertility in Mice Lacking Mitochondrial Voltage-dependent Anion Channel Type 3 von Sampson, Margaret J., Decker, William K., Beaudet, Arthur L., Ruitenbeek, Wim, Armstrong, Dawna, Hicks, M. John, Craigen, William J.

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Mouse VDAC isoforms expressed in yeast: channel properties and their roles in mitochondrial outer membrane permeability von Xu, X, Decker, W, Sampson, M J, Craigen, W J, Colombini, M

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Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome von Yatsenko, SA, Yatsenko, AN, Szigeti, K, Craigen, WJ, Stankiewicz, P, Cheung, SW, Lupski, JR

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The Role of Mitochondrial Porins and the Permeability Transition Pore in Learning and Synaptic Plasticity von Weeber, Edwin J., Levy, Michael, Sampson, Margaret J., Anflous, Keltoum, Armstrong, Dawna L., Brown, Sarah E., Sweatt, J. David, Craigen, William J.

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PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13 von Maheshwari, M., Belmont, J., Fernbach, S., Ho, T., Molinari, L., Yakub, I., Yu, F., Combes, A., Towbin, J., Craigen, W. J., Gibbs, R.

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Altered Mitochondrial Sensitivity for ADP and Maintenance of Creatine-stimulated Respiration in Oxidative Striated Muscles from VDAC1-deficient Mice von Anflous, Keltoum, Armstrong, Dawna D., Craigen, William J.

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Requirement of voltage-dependent anion channel 2 for pro-apoptotic activity of Bax von Yamagata, H, Shimizu, S, Nishida, Y, Watanabe, Y, Craigen, W J, Tsujimoto, Y

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Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization von Brunetti-Pierri, N, Grange, DK, Ou, Z, Peiffer, DA, Peacock, SKG, Cooper, ML, Eng, PA, Lalani, SR, Chinault, AC, Gunderson, KL, Craigen, WJ, Cheung, S-W

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D-2-Hydroxyglutaric aciduria: Biochemical marker or clinical disease entity? von Van Der Knaap, M. S., Jakobs, C., Hoffmann, G. F., Nyhan, W. L., Renier, W. O., Smeitink, J. A. M., Catsman-Berrevoets, C. E., Hjalmarson, O., Vallance, H., Sugita, K., Bowe, C. M., Herrin, J. T., Craigen, W. J., Buist, N. R. M., Brookfield, D. S. K., Chalmers, R. A.

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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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