Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis (English)
- New search for: Feliubadaló, Lídia
- New search for: Arbonés, María Lourdes
- New search for: Mañas, Sandra
- New search for: Chillarón, Josep
- New search for: Visa, Joana
- New search for: Rodés, Margot
- New search for: Rousaud, Ferran
- New search for: Zorzano, Antonio
- New search for: Palacín, Manuel
- New search for: Nunes, Virginia
- New search for: Feliubadaló, Lídia
- New search for: Arbonés, María Lourdes
- New search for: Mañas, Sandra
- New search for: Chillarón, Josep
- New search for: Visa, Joana
- New search for: Rodés, Margot
- New search for: Rousaud, Ferran
- New search for: Zorzano, Antonio
- New search for: Palacín, Manuel
- New search for: Nunes, Virginia
In:
Human molecular genetics
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12
, 17
;
2097-
;
2003
- Article (Journal) / Electronic Resource
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Title:Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis
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Contributors:Feliubadaló, Lídia ( author ) / Arbonés, María Lourdes ( author ) / Mañas, Sandra ( author ) / Chillarón, Josep ( author ) / Visa, Joana ( author ) / Rodés, Margot ( author ) / Rousaud, Ferran ( author ) / Zorzano, Antonio ( author ) / Palacín, Manuel ( author ) / Nunes, Virginia ( author )
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Published in:Human molecular genetics ; 12, 17 ; 2097-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-09-01
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 12, Issue 17
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 2087
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High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypesRibbhammar, Ulrica / Flornes, Line / Bäckdahl, Liselotte / Luthman, Holger / Fossum, Sigbjörn / Lorentzen, Johnny C. et al. | 2003
- 2097
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Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasisFeliubadaló, Lídia / Arbonés, María Lourdes / Mañas, Sandra / Chillarón, Josep / Visa, Joana / Rodés, Margot / Rousaud, Ferran / Zorzano, Antonio / Palacín, Manuel / Nunes, Virginia et al. | 2003
- 2109
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A mouse model for cystinuria type IPeters, T. / Thaete, C. / Wolf, S. / Popp, A. / Sedlmeier, R. / Grosse, J. / Nehls, M.C. / Russ, A. / Schlueter, V. et al. | 2003
- 2121
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Aberrant splicing induced by missense mutations in BRCA1: clues from a humanized mouse modelYang, Yongping / Swaminathan, Srividya / Martin, Betty K. / Sharan, Shyam K. et al. | 2003
- 2133
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Intrinsic susceptibility to misfolding of a hot-spot for Hirschsprung disease mutations in the ectodomain of RETKjær, Svend / Ibáñez, Carlos F. et al. | 2003
- 2145
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Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletionsYu, Wei / Ballif, Blake C. / Kashork, Catherine D. / Heilstedt, Heidi A. / Howard, Leslie A. / Cai, Wei-Wen / White, Lisa D. / Liu, Wenbin / Beaudet, Arthur L. / Bejjani, Bassem A. et al. | 2003
- 2153
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Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletionsBallif, Blake C. / Yu, Wei / Shaw, Chad A. / Kashork, Catherine D. / Shaffer, Lisa G. et al. | 2003
- 2167
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Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosomeChadwick, Brian P. / Willard, Huntington F. et al. | 2003
- 2179
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CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retinaMehalow, Adrienne K. / Kameya, Shuhei / Smith, Richard S. / Hawes, Norman L. / Denegre, James M. / Young, James A. / Bechtold, Lesley / Haider, Neena B. / Tepass, Ulrich / Heckenlively, John R. et al. | 2003
- 2191
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Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to diseaseBomprezzi, Roberto / Ringnér, Markus / Kim, Seungchan / Bittner, Michael L. / Khan, Javed / Chen, Yidong / Elkahloun, Abdel / Yu, Aimee / Bielekova, Bibiana / Meltzer, Paul S. et al. | 2003
- 2201
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Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangementsArmengol, Lluís / Pujana, Miguel Angel / Cheung, Joseph / Scherer, Stephen W. / Estivill, Xavier et al. | 2003
- 2209
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Genetic unmasking of epigenetically silenced tumor suppressor genes in colon cancer cells deficient in DNA methyltransferasesPaz, Maria F. / Wei, Susan / Cigudosa, Juan C. / Rodriguez-Perales, Sandra / Peinado, Miguel A. / Huang, Tim Hui-Ming / Esteller, Manel et al. | 2003
- 2221
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Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defectsKiefer, Susan McLeskey / Ohlemiller, Kevin K. / Yang, Jing / McDill, Bradley W. / Kohlhase, Jürgen / Rauchman, Michael et al. | 2003
- 2229
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Recombination across the centromere of disjoined and non-disjoined chromosome 21Laurent, Anne-Marie / Li, Meizhang / Sherman, Stephanie / Roizès, Gérard / Buard, Jérôme et al. | 2003
- 2241
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Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosisMerryweather-Clarke, Alison T. / Cadet, Estelle / Bomford, Adrian / Capron, Dominique / Viprakasit, Vip / Miller, Anne / McHugh, Paddy J. / Chapman, Roger W. / Pointon, Jennifer J. / Wimhurst, Victoria L.C. et al. | 2003