Exploration, normalization, and summaries of high density oligonucleotide array probe level data von Irizarry, Rafael A, Hobbs, Bridget, Collin, Francois, Beazer-Barclay, Yasmin D, Antonellis, Kristen J, Scherf, Uwe, Speed, Terence P

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HYBRIDIZATION NORMALIZATION METHODS von BEAZER-BARCLAY, YASMIN, ELASHOF, MICHAEL, SCHERF, UWE, JELINSKY, SCOTT, A, ANTONELLIS, KRISTEN, J, BROWN, EUGENE, L, WHITLEY, MARRIANE

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Hybridization normalization methods von BEAZER-BARCLAY YASMIN, ANTONELLIS KRISTEN J, ELASHOFF MICHAEL, WHITLEY MARYANN, BROWN EUGENE L, SCHERF UWE, JELINSKY SCOTT A

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HYBRIDIZATION NORMALIZATION METHODS von BEAZER-BARCLAY, YASMIN, ELASHOF, MICHAEL, SCHERF, UWE, JELINSKY, SCOTT, A, ANTONELLIS, KRISTEN, J, BROWN, EUGENE, L, WHITLEY, MARRIANE

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HYBRIDIZATION NORMALIZATION METHODS von BEAZER-BARCLAY, YASMIN, ELASHOF, MICHAEL, SCHERF, UWE, JELINSKY, SCOTT, A, ANTONELLIS, KRISTEN, J, BROWN, EUGENE, L, WHITLEY, MARRIANE

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Hybridization normalization methods von MICHAEL ELASHOF, KRISTEN J. ANTONELLIS, EUGENE L. BROWN, MARRIANE WHITLEY, SCOTT A. JELINSKY, UWE SCHERF, YASMIN BEAZER-BARCLAY

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HYBRIDIZATION NORMALIZATION METHODS von BEAZER-BARCLAY, YASMIN, ELASHOF, MICHAEL, SCHERF, UWE, JELINSKY, SCOTT, A, ANTONELLIS, KRISTEN, J, BROWN, EUGENE, L, WHITLEY, MARRIANE

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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder von Abrams, Alexander J, Hufnagel, Robert B, Rebelo, Adriana, Zanna, Claudia, Patel, Neville, Gonzalez, Michael A, Campeanu, Ion J, Griffin, Laurie B, Groenewald, Saskia, Strickland, Alleene V, Tao, Feifei, Speziani, Fiorella, Abreu, Lisa, Schüle, Rebecca, Caporali, Leonardo, La Morgia, Chiara, Maresca, Alessandra, Liguori, Rocco, Lodi, Raffaele, Ahmed, Zubair M, Sund, Kristen L, Wang, Xinjian, Krueger, Laura A, Peng, Yanyan, Prada, Carlos E, Prows, Cynthia A, Schorry, Elizabeth K, Antonellis, Anthony, Zimmerman, Holly H, Abdul-Rahman, Omar A, Yang, Yaping, Downes, Susan M, Prince, Jeffery, Fontanesi, Flavia, Barrientos, Antonio, Németh, Andrea H, Carelli, Valerio, Huang, Taosheng, Zuchner, Stephan, Dallman, Julia E

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Mutations in a Novel CLN6-Encoded Transmembrane Protein Cause Variant Neuronal Ceroid Lipofuscinosis in Man and Mouse von Gao, Hanlin, Boustany, Rose-Mary N., Espinola, Janice A., Cotman, Susan L., Srinidhi, Lakshmi, Antonellis, Kristen Auger, Gillis, Tammy, Qin, Xuebin, Liu, Shumei, Donahue, Leah R., Bronson, Roderick T., Faust, Jerry R., Stout, Derek, Haines, Jonathan L., Lerner, Terry J., MacDonald, Marcy E.

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Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L, Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L, Johnson, Kevin A, Donahue, Leah-Rae, Teed, Allison M, Antonellis, Kristen, Bronson, Roderick T, Lerner, Terry J, MacDonald, Marcy E

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Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder von Abrams, Alexander J., Hufnagel, Robert B., Rebelo, Adriana, Zanna, Claudia, Patel, Neville, Gonzalez, Michael A., Campeanu, Ion J., Griffin, Laurie B., Groenewald, Saskia, Strickland, Alleene V., Tao, Feifei, Speziani, Fiorella, Abreu, Lisa, Schüle, Rebecca, Caporali, Leonardo, La Morgia, Chiara, Maresca, Alessandra, Liguori, Rocco, Lodi, Raffaele, Ahmed, Zubair M., Sund, Kristen L., Wang, Xinjian, Krueger, Laura A., Peng, Yanyan, Prada, Carlos E., Prows, Cynthia A., Bove, Kevin, Schorry, Elizabeth K., Antonellis, Anthony, Zimmerman, Holly H., Abdul-Rahman, Omar A., Yang, Yaping, Downes, Susan M., Prince, Jeffery, Fontanesi, Flavia, Barrientos, Antonio, Nemeth, Andrea H., Carelli, Valerio, Huang, Taosheng, Zuchner, Stephan, Dallman, Julia E.

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An Ugo1-like protein is associated with optic atrophy ‘plus’ disorders von Abrams, Alexander J., Hufnagel, Robert B., Rebelo, Adriana, Zanna, Claudia, Patel, Neville, Gonzalez, Michael A., Campeanu, Ion J., Griffin, Laurie B., Groenewald, Saskia, Strickland, Alleene V., Tao, Feifei, Speziani, Fiorella, Caporali, Leonardo, La Morgia, Chiara, Liguori, Rocco, Lodi, Raffaele, Ahmed, Zubair M., Sund, Kristen L., Wang, Xinjian, Krueger, Laura A., Peng, Yanyan, Prada, Carlos E., Prows, Cynthia A., Bove, Kevin, Schorry, Elizabeth K., Antonellis, Anthony, Zimmerman, Holly H., Abdulrahman, Omar A., Yang, Yaping, Downes, Susan M., Prince, Jeffery, Nemeth, Andrea H., Carelli, Valerio, Huang, Taosheng, Julia, Dallman, Zuchner, Stephan

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Cln3 Δex7/8 knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth von Cotman, Susan L., Vrbanac, Vladimir, Lebel, Lori-Anne, Lee, Richard L., Johnson, Kevin A., Donahue, Leah-Rae, Teed, Allison M., Antonellis, Kristen, Bronson, Roderick T., Lerner, Terry J., MacDonald, Marcy E.

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