The CDY-related gene family: coordinated evolution in copy number, expression profile and protein sequence (English)
- New search for: Dorus, Steve
- New search for: Gilbert, Sandra L.
- New search for: Forster, Michele L.
- New search for: Barndt, Robert J.
- New search for: Lahn, Bruce T.
- New search for: Dorus, Steve
- New search for: Gilbert, Sandra L.
- New search for: Forster, Michele L.
- New search for: Barndt, Robert J.
- New search for: Lahn, Bruce T.
In:
Human molecular genetics
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12
, 14
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1643-
;
2003
- Article (Journal) / Electronic Resource
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Title:The CDY-related gene family: coordinated evolution in copy number, expression profile and protein sequence
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Contributors:Dorus, Steve ( author ) / Gilbert, Sandra L. ( author ) / Forster, Michele L. ( author ) / Barndt, Robert J. ( author ) / Lahn, Bruce T. ( author )
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Published in:Human molecular genetics ; 12, 14 ; 1643-
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Publisher:
- New search for: Oxford University Press
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Publication date:2003-07-15
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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 14
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.
- 1643
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The CDY-related gene family: coordinated evolution in copy number, expression profile and protein sequenceDorus, Steve / Gilbert, Sandra L. / Forster, Michele L. / Barndt, Robert J. / Lahn, Bruce T. et al. | 2003
- 1651
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Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locusBadano, Jose L. / Kim, Jun Chul / Hoskins, Bethan E. / Lewis, Richard Alan / Ansley, Stephen J. / Cutler, David J. / Castellan, Claudio / Beales, Philip L. / Leroux, Michel R. / Katsanis, Nicholas et al. | 2003
- 1661
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Upregulation of the transcription factor TFEB in t(6;11)(p21;q13)-positive renal cell carcinomas due to promoter substitutionKuiper, Roland P. / Schepens, Marga / Thijssen, José / van Asseldonk, Martien / van den Berg, Eva / Bridge, Julia / Schuuring, Ed / Schoenmakers, Eric F.P.M. / van Kessel, Ad Geurts et al. | 2003
- 1671
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ALS2, a novel guanine nucleotide exchange factor for the small GTPase Rab5, is implicated in endosomal dynamicsOtomo, Asako / Hadano, Shinji / Okada, Takeya / Mizumura, Hikaru / Kunita, Ryota / Nishijima, Hitoshi / Showguchi-Miyata, Junko / Yanagisawa, Yoshiko / Kohiki, Eri / Suga, Etsuko et al. | 2003
- 1689
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82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localizationBardoni, Barbara / Castets, Marie / Huot, Marc-Etienne / Schenck, Annette / Adinolfi, Salvatore / Corbin, François / Pastore, Annalisa / Khandjian, Edouard W. / Mandel, Jean-Louis et al. | 2003
- 1699
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Decreased expression of genes involved in sulfur amino acid metabolism in frataxin-deficient cellsTan, Guolin / Napoli, Eleonora / Taroni, Franco / Cortopassi, Gino et al. | 2003
- 1713
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Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nervePrevitali, Stefano C. / Zerega, Barbara / Sherman, Diane L. / Brophy, Peter J. / Dina, Giorgia / King, Rosalind H.M. / Salih, Mustafa M. / Feltri, Laura / Quattrini, Angelo / Ravazzolo, Roberto et al. | 2003
- 1725
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A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactylyLettice, Laura A. / Heaney, Simon J.H. / Purdie, Lorna A. / Li, Li / de Beer, Philippe / Oostra, Ben A. / Goode, Debbie / Elgar, Greg / Hill, Robert E. / de Graaff, Esther et al. | 2003
- 1737
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Targeted epidermal expression of mutant Connexin 26(D66H) mimics true Vohwinkel syndrome and provides a model for the pathogenesis of dominant connexin disordersBakirtzis, George / Choudhry, Rukhsana / Aasen, Trond / Shore, Leonard / Brown, Ken / Bryson, Sheila / Forrow, Stephen / Tetley, Laurence / Finbow, Malcolm / Greenhalgh, David et al. | 2003
- 1745
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Association of 5' estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture riskvan Meurs, Joyce B.J. / Schuit, Stephanie C.E. / Weel, Angélique E.A.M. / van der Klift, Marjolein / Bergink, Arjan P. / Arp, Pascal P. / Colin, Edgar M. / Fang, Yue / Hofman, Albert / van Duijn, Cornelia M. et al. | 2003
- 1755
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Dimerization of SOX9 is required for chondrogenesis, but not for sex determinationBernard, Pascal / Tang, Paisu / Liu, Siyuan / Dewing, Phoebe / Harley, Vincent R. / Vilain, Eric et al. | 2003
- 1767
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Cell cycle-dependent translation of p27 involves a responsive element in its 5'-UTR that overlaps with a uORFGöpfert, Ulrich / Kullmann, Michael / Hengst, Ludger et al. | 2003
- 1781
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Association and linkage analyses of RGS4 polymorphisms in schizophreniaChowdari, Kodavali V. / Mirnics, Karoly / Semwal, Prachi / Wood, Joel / Lawrence, Elizabeth / Bhatia, Triptish / Deshpande, Smita N. / Thelma, B.K. / Ferrell, Robert E. / Middleton, Frank A. et al. | 2003