Galloway

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Homozygous splicing mutation in NUP133 causes Galloway–Mowat syndrome von Fujita, Atsushi, Tsukaguchi, Hiroyasu, Koshimizu, Eriko, Nakazato, Hitoshi, Itoh, Kyoko, Kuraoka, Shohei, Komohara, Yoshihiro, Shiina, Masaaki, Nakamura, Shohei, Kitajima, Mika, Tsurusaki, Yoshinori, Miyatake, Satoko, Ogata, Kazuhiro, Iijima, Kazumoto, Matsumoto, Naomichi, Miyake, Noriko

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Mutations in WDR4 as a new cause of Galloway–Mowat syndrome von Braun, Daniela A., Shril, Shirlee, Sinha, Aditi, Schneider, Ronen, Tan, Weizhen, Ashraf, Shazia, Hermle, Tobias, Jobst‐Schwan, Tilman, Widmeier, Eugen, Majmundar, Amar J., Daga, Ankana, Warejko, Jillian K., Nakayama, Makiko, Schapiro, David, Chen, Jing, Airik, Merlin, Rao, Jia, Schmidt, Johanna Magdalena, Hoogstraten, Charlotte A., Hugo, Hannah, Meena, Jitendra, Lek, Monkol, Laricchia, Kristen M., Bagga, Arvind, Hildebrandt, Friedhelm

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Reprogramming Stars #8: A Synthetic Biology Approach to Cellular Reprogramming-An Interview with Dr. Katie Galloway von Galloway, Kate E, Pereira, Carlos-Filipe

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In Memoriam: Patricia D. Galloway von Singh, Amarjit

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Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome von Treimer, Ernestine, Kalayci, Tugba, Schumann, Sven, Suer, Ilknur, Greco, Sara, Schanze, Denny, Schmeisser, Michael J., Kühl, Susanne J., Zenker, Martin

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Disruption of pathways regulated by Integrator complex in Galloway–Mowat syndrome due to WDR73 mutations von Tilley, F. C., Arrondel, C., Chhuon, C., Boisson, M., Cagnard, N., Parisot, M., Menara, G., Lefort, N., Guerrera, I. C., Bole-Feysot, C., Benmerah, A., Antignac, C., Mollet, G.

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Folk Fantail, Missing you-Kotare, Sunshine Kereru, Loyal Hihi, and Morning Quails by Jane Galloway von Wentz, Margaret R.

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Correction: A 20 bp Duplication in Exon 2 of the Aristaless-Like Homeobox 4 Gene (ALX4) Is the Candidate Causative Mutation for Tibial Hemimelia Syndrome in Galloway Cattle von Brenig, Bertram, Schütz, Ekkehard, Hardt, Michael, Scheuermann, Petra, Freick, Markus

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Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome von Mann, Nina, Mzoughi, Slim, Schneider, Ronen, Kühl, Susanne J, Schanze, Denny, Klämbt, Verena, Lovric, Svjetlana, Mao, Youying, Shi, Shasha, Tan, Weizhen, Kühl, Michael, Onuchic-Whitford, Ana C, Treimer, Ernestine, Kitzler, Thomas M, Kause, Franziska, Schumann, Sven, Nakayama, Makiko, Buerger, Florian, Shril, Shirlee, van der Ven, Amelie T, Majmundar, Amar J, Holton, Kristina Marie, Kolb, Amy, Braun, Daniela A, Rao, Jia, Jobst-Schwan, Tilman, Mildenberger, Eva, Lennert, Thomas, Kuechler, Alma, Wieczorek, Dagmar, Gross, Oliver, Ermisch-Omran, Beate, Werberger, Anja, Skalej, Martin, Janecke, Andreas R, Soliman, Neveen A, Mane, Shrikant M, Lifton, Richard P, Kadlec, Jan, Guccione, Ernesto, Schmeisser, Michael J, Zenker, Martin, Hildebrandt, Friedhelm

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BETWEEN SUMNER AND GALTON: A FURTHER LOOK AT ALBERT GALLOWAY KELLER’S SOCIOLOGY von Fiorito, Luca, Erasmo, Valentina

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High-risk HPV mRNA testing on self-samples offered to those who do not attend for organised cervical screening – real world data from the Dumfries and Galloway region in Scotland von Forson, William, Bhatia, Ramya, Currie, Heather, Elasifer, Hana, Connor, Linzi, Wilson, Allan, Cuschieri, Kate

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Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome von Colin, Estelle, Huynh Cong, Evelyne, Mollet, Géraldine, Guichet, Agnès, Gribouval, Olivier, Arrondel, Christelle, Boyer, Olivia, Daniel, Laurent, Gubler, Marie-Claire, Ekinci, Zelal, Tsimaratos, Michel, Chabrol, Brigitte, Boddaert, Nathalie, Verloes, Alain, Chevrollier, Arnaud, Gueguen, Naig, Desquiret-Dumas, Valérie, Ferré, Marc, Procaccio, Vincent, Richard, Laurence, Funalot, Benoit, Moncla, Anne, Bonneau, Dominique, Antignac, Corinne

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New Species of the Superfamily Palaeotextularioidea Galloway von Sakhnenko, K. V

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Hepatic Lipodystrophy in Galloway Calves von Wieland, M., Mann, S., Hafner-Marx, A., Ignatius, A., Metzner, M.

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Galloway… living in his own bubble von Morley, David

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Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localization von Teng, Hua, Liang, Chen, Liang, Desheng, Li, Zhuo, Wu, Lingqian

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Neuropathologic Findings in Galloway-Mowat Syndrome 3 With a Novel OSGEP Variant von Baker, Tiffany, Caylor, Raymond, Wang, Jiyong, Kilpatrick, Matthew, Batalis, Nicholas, Wolff, Daynna, Welsh, Cynthia

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WDR73-related galloway mowat syndrome with collapsing glomerulopathy von El Younsi, Mariem, Kraoua, Lilia, Meddeb, Rym, Ferjani, Maryem, Trabelsi, Médiha, Ouertani, Ines, Maazoul, Faouzi, Abid, Nabil, Gargah, Tahar, M'rad, Ridha

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A patient diagnosed with Galloway–Mowat syndrome presenting with a rod-cone functional anomaly with electronegative dark-adapted ERGs von Racine, Julie, Golden, Richard

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