Mechanism of Crystal Formation in Ruddlesden–Popper Sn‐Based Perovskites von Dong, Jingjin, Shao, Shuyan, Kahmann, Simon, Rommens, Alexander J., Hermida‐Merino, Daniel, ten Brink, Gert H., Loi, Maria A., Portale, Giuseppe

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Gastric Embolization as Treatment for Overweight Patients; Efficacy and Safety von Elens, S., Roger, T., Elens, M., Rommens, J., Sarafidis, A., Capelluto, E., Delcour, C.

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Cloning and Mapping of a cDNA for Methionine Synthase Reductase, a Flavoprotein Defective in Patients with Homocystinuria von Leclerc, D., Wilson, A., Dumas, R., Gafuik, C., Song, D., Watkins, D., Heng, H. H. Q., Rommens, J. M., Scherer, S. W., Rosenblatt, D. S., Gravel, R. A.

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Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes von Zambetti, Noemi A, Bindels, Eric M J, Van Strien, Paulina M H, Valkhof, Marijke G, Adisty, Maria N, Hoogenboezem, Remco M, Sanders, Mathijs A, Rommens, Johanna M, Touw, Ivo P, Raaijmakers, Marc H G P

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Mutations in SBDS are associated with Shwachman-Diamond syndrome von Rommens, Johanna M, Boocock, Graeme R.B, Morrison, Jodi A, Popovic, Maja, Richards, Nicole, Ellis, Lynda, Durie, Peter R

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Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly von Belloni, E, Muenke, M, Roessler, E, Traverse, G, Siegel-Bartelt, J, Frumkin, A, Mitchell, H.F, Donis-Keller, H, Helms, C, Hing, A.V, Heng, H.H.Q, Koop, B, Martindale, D, Rommens, J.M, Tsui, L.-C, Scherer, S.W

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene ( UBE3A ) in Angelman syndrome von Matsuura, Toshinobu, Sutcliffe, James S, Fang, Ping, Galjaard, Robert-Jan, Jiang, Yong-hui, Benton, Claudia S, Rommens, Johanna M, Beaudet, Arthur L

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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy von Rouleau, Guy A, Nohira, Osamu, Mathieu, Jean, Heutink, Peter, Duranceau, André, Codère, Francois, Fardeau, Michel, Brais, Bernard, Korcyn, Amos D, Chrétien, Nathalie, Rochefort, Daniel L, Tomé, Fernando M.S, Xie, Ya-Gang, Rommens, Johanna M, Blumen, Segiu, Lafrentére, Ronald G, Uyama, Eichiro, Bouchard, Jean-Pierre

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Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene von Rogaev, E. I, Sherrington, R, Rogaeva, E. A, Levesque, G, Ikeda, M, Liang, Y, Chi, H, Lin, C, Holman, K, Tsuda, T, Mar, L, Sorbi, S, Nacmias, B, Piacentini, S, Amaducci, L, Chumakov, I, Cohen, D, Lannfelt, L, Fraser, P. E, Rommens, J. M, George-Hyslop, P. H. St

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Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease von Sherrington, R., Rogaev, E. I., Liang, Y., Rogaeva, E. A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Li, G., Holman, K., Tsuda, T., Mar, L., Foncin, J.-F., Bruni, A. C., Montesi, M. P., Sorbi, S., Rainero, I., Pinessi, L., Nee, L., Chumakov, I., Pollen, D., Brookes, A., Sanseau, P., Polinsky, R. J., Wasco, W., Da Silva, H. A. R., Haines, J. L., Pericak-Vance, M. A., Tanzi, R. E., Roses, A. D., Fraser, P. E., Rommens, J. M., St George-Hyslop, P. H.

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Shwachman syndrome: Phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar von Ginzberg, Hedy, Shin, Janey, Ellis, Lynda, Morrison, Jodi, Ip, Wan, Dror, Yigal, Freedman, Melvin, Heitlinger, Leo A., Belt, Mary Ann, Corey, Mary, Rommens, Johanna M., Durie, Peter R.

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Phylogeny, sequence conservation, and functional complementation of the SBDS protein family von Boocock, G.R.B., Marit, M.R., Rommens, J.M.

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Grain‐Specific Transitions Determine the Band Edge Luminescence in Dion–Jacobson Type 2D Perovskites von Kahmann, Simon, Duim, Herman, Rommens, Alexander J., Tekelenburg, Eelco K., Shao, Shuyan, Loi, Maria A.

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Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS von Mäkitie, O, Ellis, L, Durie, PR, Morrison, JA, Sochett, EB, Rommens, JM, Cole, WG

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Taking a closer look - how the microstructure of Dion-Jacobson perovskites governs their photophysics von Kahmann, Simon, Duim, Herman, Rommens, Alexander J, Frohna, Kyle, ten Brink, Gert H, Portale, Giuseppe, Stranks, Samuel D, Loi, Maria A

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Crystal Formation: Mechanism of Crystal Formation in Ruddlesden–Popper Sn‐Based Perovskites (Adv. Funct. Mater. 24/2020) von Dong, Jingjin, Shao, Shuyan, Kahmann, Simon, Rommens, Alexander J., Hermida‐Merino, Daniel, ten Brink, Gert H., Loi, Maria A., Portale, Giuseppe

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Identification of the Cystic Fibrosis Gene: Genetic Analysis von Kerem, Bat-sheva, Rommens, Johanna M., Buchanan, Janet A., Markiewicz, Danuta, Cox, Tara K., Chakravarti, Aravinda, Buchwald, Manuel, Tsui, Lap-Chee

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Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant von Sherrington, R., Froelich, S., Sorbi, S., Campion, D., Chi, H., Rogaeva, E. A., Levesque, G., Rogaev, E. I., Lin, C., Liang, Y., Ikeda, M., Mar, L., Brice, A., Agid, Y., Percy, M.E., Clerget-Darpoux, F., Piacentini, S., Marcon, G., Nacmias, B., Amaducci, L., Frebourg, T., Lannfelt, L., Rommens, J. M., St George-Hyslop, P. H.

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The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene von Bull, Peter C, Thomas, Gordon R, Rommens, Johanna M, Forbes, John R, Cox, Diane Wilson

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Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA von Riordan, John R., Rommens, Johanna M., Kerem, Bat-sheva, Alon, Noa, Rozmahel, Richard, Grzelczak, Zbyszko, Zielenski, Julian, Lok, Si, Plavsic, Natasa, Chou, Jia-Ling, Drumm, Mitchell L., Iannuzzi, Michael C., Collins, Francis S., Tsui, Lap-Chee

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