CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development von Geller, Scott F, Guerin, Karen I, Visel, Meike, Pham, Aaron, Lee, Edwin S, Dror, Amiel A, Avraham, Karen B, Hayashi, Toshinori, Ray, Catherine A, Reh, Thomas A, Bermingham-McDonogh, Olivia, Triffo, William J, Bao, Shaowen, Isosomppi, Juha, Västinsalo, Hanna, Sankila, Eeva-Marja, Flannery, John G

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The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain von Holmberg, Ville, Jalanko, Anu, Isosomppi, Juha, Fabritius, Anna-Liisa, Peltonen, Leena, Kopra, Outi

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Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain von Tian, Guilian, Zhou, Yun, Hajkova, Dagmar, Miyagi, Masaru, Dinculescu, Astra, Hauswirth, William W., Palczewski, Krzysztof, Geng, Ruishuang, Alagramam, Kumar N., Isosomppi, Juha, Sankila, Eeva-Marja, Flannery, John G., Imanishi, Yoshikazu

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Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein von Isosomppi, Juha, Vesa, Jouni, Jalanko, Anu, Peltonen, Leena

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Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON von Tian, Guilian, Zhou, Yun, Hajkova, Dagmar, Miyagi, Masaru, Dinculescu, Astra, Hauswirth, William W, Palczewski, Krzysztof, Geng, Ruishuang, Alagramam, Kumar N, Isosomppi, Juha, Sankila, Eeva-Marja, Flannery, John G, Imanishi, Yoshikazu

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Speech recognition and communication outcomes with cochlear implantation in Usher syndrome type 3 von Pietola, Laura, Aarnisalo, Antti A, Abdel-Rahman, Akram, Västinsalo, Hanna, Isosomppi, Juha, Löppönen, Heikki, Kentala, Erna, Johansson, Reijo, Valtonen, Hannu, Vasama, Juha-Pekka, Sankila, Eeva-Marja, Jero, Jussi

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Alternative splice variants of the USH3A gene Clarin 1 (CLRN1) von VÄSTINSALO, Hanna, JALKANEN, Reetta, DINCULESCU, Astra, ISOSOMPPI, Juha, GELLER, Scott, FLANNERY, John G, HAUSWIRTH, William W, SANKILA, Eeva-Marja

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Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane von Isosomppi, Juha, Västinsalo, Hanna, Geller, Scott F, Heon, Elise, Flannery, John G, Sankila, Eeva-Marja

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Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3 von Vesa, Jouni, Chin, Mark H, Oelgeschläger, Kathrin, Isosomppi, Juha, DellAngelica, Esteban C, Jalanko, Anu, Peltonen, Leena

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MATTRESS FOR AEROPLANE von ISOSOMPPI, Juha

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MATTRESS FOR AEROPLANE von ISOSOMPPI, Juha

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MATTRESS FOR AEROPLANE von ISOSOMPPI, Juha

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Patja lentokoneeseen von Isosomppi, Juha

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Two Finnish USH1B patients with three novel mutations in myosin VIIA von Vastinsalo, Hanna, Isosomppi, Juha, Aittakorpi, Anne, Sankila, Eeva-Marja

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CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development: e1000607 von Geller, Scott F, Guerin, Karen I, Visel, Meike, Pham, Aaron, Lee, Edwin S, Dror, Amiel A, Avraham, Karen B, Hayashi, Toshinori, Ray, Catherine A, Reh, Thomas A, Bermingham-McDonogh, Olivia, Triffo, William J, Bao, Shaowen, Isosomppi, Juha, Västinsalo, Hanna, Sankila, Eeva-Marja, Flannery, John G

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Toward Cloning of a Novel Ataxia Gene: Refined Assignment and Physical Map of the IOSCA Locus (SCA8) on 10q24 von Nikali, Kaisu, Isosomppi, Juha, Lönnqvist, Tuula, Mao, Jen-i, Suomalainen, Anu, Peltonen, Leena

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Positional Cloning of the CLN5 Gene Defective in the Finnish Variant of the LINCL von Klockars, Tuomas, Savukoski, Minna, Isosomppi, Juha, Peltonen, Leena

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Utilization of FISH in positional cloning: an example on 13q22 von Laan, M, Isosomppi, J, Klockars, T, Peltonen, L, Palotie, A

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A Physical Map of the 6q14–q15 Region Harboring the Locus for the Lysosomal Membrane Sialic Acid Transport Defect von Leppänen, Pirjo, Isosomppi, Juha, Schleutker, Johanna, Aula, Pertti, Peltonen, Leena

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Developmental expression of palmitoyl protein thioesterase in normal mice von Isosomppi, Juha, Heinonen, Outi, Hiltunen, Jukka O, Greene, Nicholas D.E, Vesa, Jouni, Uusitalo, Annukka, Mitchison, Hannah M, Saarma, Mart, Jalanko, Anu, Peltonen, Leena

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