My NCBI | Sign In
RSS Settings
  • Search: Veitia RA[au]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

    Results: 1 to 50 of 69

    1.

    The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution.

    Birchler JA, Veitia RA.

    New Phytol. 2009 Nov 19. [Epub ahead of print]PMID: 19925558 [PubMed - as supplied by publisher]Related articles

    2.

    Dominance and gene dosage balance in health and disease: why levels matter!

    Veitia RA, Birchler JA.

    J Pathol. 2009 Oct 13. [Epub ahead of print]PMID: 19827001 [PubMed - as supplied by publisher]Related articles

    3.

    Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?

    Georges AB, Benayoun BA, Caburet S, Veitia RA.

    FASEB J. 2009 Sep 17. [Epub ahead of print]PMID: 19762556 [PubMed - as supplied by publisher]Related articles

    4.

    The forkhead factor FOXL2: A novel tumor suppressor?

    Benayoun BA, Kalfa N, Sultan C, Veitia RA.

    Biochim Biophys Acta. 2009 Sep 10. [Epub ahead of print]PMID: 19747961 [PubMed - as supplied by publisher]Related articles

    5.

    The new molecular biology of granulosa cell tumors of the ovary.

    Kalfa N, Veitia RA, Benayoun BA, Boizet-Bonhoure B, Sultan C.

    Genome Med. 2009 Aug 25;1(8):81.PMID: 19725933 [PubMed - in process]Related articlesFree article

    6.

    Extensive sequence turnover of the signal peptides of members of the GDF/BMP family: exploring their evolutionary landscape.

    Veitia RA, Caburet S.

    Biol Direct. 2009 Jul 16;4:22.PMID: 19607682 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Dominant negative factors in health and disease.

    Veitia RA.

    J Pathol. 2009 Aug;218(4):409-18. Review.PMID: 19544283 [PubMed - indexed for MEDLINE]Related articles

    8.

    Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.

    Dipietromaria A, Benayoun BA, Todeschini AL, Rivals I, Bazin C, Veitia RA.

    Hum Mol Genet. 2009 Sep 1;18(17):3324-33. Epub 2009 Jun 10.PMID: 19515849 [PubMed - indexed for MEDLINE]Related articles

    9.

    BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?

    Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA.

    Clin Endocrinol (Oxf). 2009 Jun 8. [Epub ahead of print] No abstract available. PMID: 19508678 [PubMed - as supplied by publisher]Related articles

    10.

    A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure.

    Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA.

    Clin Endocrinol (Oxf). 2009 Nov;71(5):752-3. Epub 2009 May 8. No abstract available. PMID: 19486016 [PubMed - in process]Related articles

    11.

    Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.

    Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, Elghezal H, Philibert P, Saâd A, Sultan C, Fellous M, Veitia RA.

    J Med Genet. 2009 Jul;46(7):455-7. Epub 2009 May 7.PMID: 19429596 [PubMed - indexed for MEDLINE]Related articles

    12.

    A post-translational modification code for transcription factors: sorting through a sea of signals.

    Benayoun BA, Veitia RA.

    Trends Cell Biol. 2009 May;19(5):189-97. Epub 2009 Mar 26.PMID: 19328693 [PubMed - indexed for MEDLINE]Related articles

    13.

    On gene dosage balance in protein complexes: a comment on Semple JI, Vavouri T, Lehner B. A simple principle concerning the robustness of protein complex activity to changes in gene expression.

    Veitia RA.

    BMC Syst Biol. 2009 Jan 30;3:16. No abstract available. PMID: 19183469 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Positive and negative feedback regulates the transcription factor FOXL2 in response to cell stress: evidence for a regulatory imbalance induced by disease-causing mutations.

    Benayoun BA, Batista F, Auer J, Dipietromaria A, L'Hôte D, De Baere E, Veitia RA.

    Hum Mol Genet. 2009 Feb 15;18(4):632-44. Epub 2008 Nov 14.PMID: 19010791 [PubMed - indexed for MEDLINE]Related articles

    15.

    One thousand and one ways of making functionally similar transcriptional enhancers.

    Veitia RA.

    Bioessays. 2008 Nov;30(11-12):1052-7. Review.PMID: 18937349 [PubMed - indexed for MEDLINE]Related articles

    16.

    Amino acid repeats and the structure and evolution of proteins.

    Albà MM, Tompa P, Veitia RA.

    Genome Dyn. 2007;3:119-30. Review.PMID: 18753788 [PubMed - indexed for MEDLINE]Related articles

    17.

    Gene expression regulation in the context of mouse interspecific mosaic genomes.

    L'Hôte D, Serres C, Veitia RA, Montagutelli X, Oulmouden A, Vaiman D.

    Genome Biol. 2008;9(8):R133. Epub 2008 Aug 27.PMID: 18752664 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Preservation of genes involved in sterol metabolism in cholesterol auxotrophs: facts and hypotheses.

    Vinci G, Xia X, Veitia RA.

    PLoS One. 2008 Aug 6;3(8):e2883.PMID: 18682733 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

    Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E.

    Hum Mutat. 2008 Nov;29(11):E205-19.PMID: 18642388 [PubMed - indexed for MEDLINE]Related articles

    20.

    The identification and characterization of a FOXL2 response element provides insights into the pathogenesis of mutant alleles.

    Benayoun BA, Caburet S, Dipietromaria A, Bailly-Bechet M, Batista F, Fellous M, Vaiman D, Veitia RA.

    Hum Mol Genet. 2008 Oct 15;17(20):3118-27. Epub 2008 Jul 16.PMID: 18635577 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    The post-translational modification profile of the forkhead transcription factor FOXL2 suggests the existence of parallel processive/concerted modification pathways.

    Benayoun BA, Auer J, Caburet S, Veitia RA.

    Proteomics. 2008 Aug;8(15):3118-23.PMID: 18604817 [PubMed - indexed for MEDLINE]Related articles

    22.

    Cellular reactions to gene dosage imbalance: genomic, transcriptomic and proteomic effects.

    Veitia RA, Bottani S, Birchler JA.

    Trends Genet. 2008 Aug;24(8):390-7. Epub 2008 Jun 26. Review.PMID: 18585818 [PubMed - indexed for MEDLINE]Related articles

    23.

    Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients.

    Nallathambi J, Laissue P, Batista F, Benayoun BA, Lesaffre C, Moumné L, Pandaranayaka PE, Usha K, Krishnaswamy S, Sundaresan P, Veitia RA.

    Hum Mutat. 2008 May 16;29(8):E123-E131. [Epub ahead of print]PMID: 18484667 [PubMed - as supplied by publisher]Related articles

    24.

    Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy.

    Hemadevi B, Veitia RA, Srinivasan M, Arunkumar J, Prajna NV, Lesaffre C, Sundaresan P.

    Arch Ophthalmol. 2008 May;126(5):700-8.PMID: 18474783 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD).

    Hersmus R, Kalfa N, de Leeuw B, Stoop H, Oosterhuis JW, de Krijger R, Wolffenbuttel KP, Drop SL, Veitia RA, Fellous M, Jaubert F, Looijenga LH.

    J Pathol. 2008 May;215(1):31-8.PMID: 18348162 [PubMed - indexed for MEDLINE]Related articles

    26.

    Recent advances in the study of genes involved in non-syndromic premature ovarian failure.

    Laissue P, Vinci G, Veitia RA, Fellous M.

    Mol Cell Endocrinol. 2008 Jan 30;282(1-2):101-11. Epub 2007 Nov 19. Review.PMID: 18164539 [PubMed - indexed for MEDLINE]Related articles

    27.

    Differential aggregation and functional impairment induced by polyalanine expansions in FOXL2, a transcription factor involved in cranio-facial and ovarian development.

    Moumné L, Dipietromaria A, Batista F, Kocer A, Fellous M, Pailhoux E, Veitia RA.

    Hum Mol Genet. 2008 Apr 1;17(7):1010-9. Epub 2007 Dec 24.PMID: 18158309 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    The mutations and potential targets of the forkhead transcription factor FOXL2.

    Moumné L, Batista F, Benayoun BA, Nallathambi J, Fellous M, Sundaresan P, Veitia RA.

    Mol Cell Endocrinol. 2008 Jan 30;282(1-2):2-11. Epub 2007 Nov 19. Review.PMID: 18155828 [PubMed - indexed for MEDLINE]Related articles

    29.

    Exploring the molecular etiology of dominant-negative mutations.

    Veitia RA.

    Plant Cell. 2007 Dec;19(12):3843-51. Epub 2007 Dec 14. Review. No abstract available. PMID: 18083908 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    FOXO3a variants in patients with premature ovarian failure.

    Vinci G, Christin-Maitre S, Pasquier M, Bouchard P, Fellous M, Veitia RA.

    Clin Endocrinol (Oxf). 2008 Mar;68(3):495-7. Epub 2007 Sep 19. No abstract available. PMID: 17888023 [PubMed - indexed for MEDLINE]Related articles

    31.

    Commonalities in fly embryogenesis and mammalian pituitary patterning.

    Veitia RA, Salazar-Ciudad I.

    Trends Endocrinol Metab. 2007 Sep;18(7):261-5. Epub 2007 Aug 10. Review.PMID: 17693094 [PubMed - indexed for MEDLINE]Related articles

    32.

    Protein coevolution and isoexpression in yeast macromolecular complexes.

    Ettwiller L, Veitia RA.

    Comp Funct Genomics. 2007:58721. Epub 2007 Jan 8.PMID: 17538690 [PubMed - in process]Related articlesFree article

    33.

    Mutations in the NOG gene are not a common cause of nonsyndromic premature ovarian failure.

    Laissue P, Christin-Maitre S, Bouchard P, Fellous M, Veitia RA.

    Clin Endocrinol (Oxf). 2007 Jun;66(6):900. Epub 2007 Mar 23. No abstract available. PMID: 17381491 [PubMed - indexed for MEDLINE]Related articles

    34.

    Potential targets of FOXL2, a transcription factor involved in craniofacial and follicular development, identified by transcriptomics.

    Batista F, Vaiman D, Dausset J, Fellous M, Veitia RA.

    Proc Natl Acad Sci U S A. 2007 Feb 27;104(9):3330-5. Epub 2007 Feb 20.PMID: 17360647 [PubMed - indexed for MEDLINE]Related articlesFree article

    35.

    The gene balance hypothesis: from classical genetics to modern genomics.

    Birchler JA, Veitia RA.

    Plant Cell. 2007 Feb;19(2):395-402. Epub 2007 Feb 9. Review. No abstract available. PMID: 17293565 [PubMed - indexed for MEDLINE]Related articlesFree article

    36.

    Recovery of female fertility after chemotherapy, irradiation, and bone marrow allograft: further evidence against massive oocyte regeneration by bone marrow-derived germline stem cells.

    Veitia RA, Gluckman E, Fellous M, Soulier J.

    Stem Cells. 2007 May;25(5):1334-5. Epub 2007 Jan 25. No abstract available. PMID: 17255517 [PubMed - indexed for MEDLINE]Related articlesFree article

    37.

    Highly constrained proteins contain an unexpectedly large number of amino acid tandem repeats.

    Mularoni L, Veitia RA, Albà MM.

    Genomics. 2007 Mar;89(3):316-25. Epub 2006 Dec 28.PMID: 17196365 [PubMed - indexed for MEDLINE]Related articles

    38.

    A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction.

    Nallathambi J, Moumné L, De Baere E, Beysen D, Usha K, Sundaresan P, Veitia RA.

    Hum Genet. 2007 Mar;121(1):107-12. Epub 2006 Nov 7.PMID: 17089161 [PubMed - indexed for MEDLINE]Related articles

    39.

    Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita.

    Laissue P, Copelli S, Bergada I, Bergada C, Barrio G, Karaboga S, Wurtz JM, Fellous M, Lalli E, Veitia RA.

    Clin Endocrinol (Oxf). 2006 Nov;65(5):681-6.PMID: 17054473 [PubMed - indexed for MEDLINE]Related articles

    40.

    Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.

    Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, Aittomaki K, Bourcigaux N, Jacquesson L, Bouchard P, Frydman R, Dewailly D, Reyss AC, Jeffery L, Bachelot A, Massin N, Fellous M, Veitia RA.

    Eur J Endocrinol. 2006 May;154(5):739-44.PMID: 16645022 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    [Translational restart downstream of a premature stop codon and protein aggregation]

    Moumné L, Veitia RA.

    Med Sci (Paris). 2006 Mar;22(3):232-4. French. No abstract available. PMID: 16527196 [PubMed - indexed for MEDLINE]Related articles

    42.

    The robustness of the transcriptional response to alterations in morphogenetic gradients.

    Veitia RA, Nijhout HF.

    Bioessays. 2006 Mar;28(3):282-9.PMID: 16479586 [PubMed - indexed for MEDLINE]Related articles

    43.

    Reverse transcriptase template switching and false alternative transcripts.

    Cocquet J, Chong A, Zhang G, Veitia RA.

    Genomics. 2006 Jul;88(1):127-31. Epub 2006 Feb 2.PMID: 16457984 [PubMed - indexed for MEDLINE]Related articles

    44.

    Deletions in the polyAlanine-containing transcription factor FOXL2 lead to intranuclear aggregation.

    Moumné L, Fellous M, Veitia RA.

    Hum Mol Genet. 2005 Dec 1;14(23):3557-64. Epub 2005 Oct 11.PMID: 16219626 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome.

    Beysen D, Raes J, Leroy BP, Lucassen A, Yates JR, Clayton-Smith J, Ilyina H, Brooks SS, Christin-Maitre S, Fellous M, Fryns JP, Kim JR, Lapunzina P, Lemyre E, Meire F, Messiaen LM, Oley C, Splitt M, Thomson J, Van de Peer Y, Veitia RA, De Paepe A, De Baere E.

    Am J Hum Genet. 2005 Aug;77(2):205-18. Epub 2005 Jun 16.PMID: 15962237 [PubMed - indexed for MEDLINE]Related articlesFree article

    46.

    Coding repeats and evolutionary "agility".

    Caburet S, Cocquet J, Vaiman D, Veitia RA.

    Bioessays. 2005 Jun;27(6):581-7. Review.PMID: 15892112 [PubMed - indexed for MEDLINE]Related articles

    47.

    Stochasticity or the fatal 'imperfection' of cloning.

    Veitia RA.

    J Biosci. 2005 Feb;30(1):21-30. Review.PMID: 15824438 [PubMed - indexed for MEDLINE]Related articlesFree article

    48.

    Sense and antisense Foxl2 transcripts in mouse.

    Cocquet J, Pannetier M, Fellous M, Veitia RA.

    Genomics. 2005 May;85(5):531-41.PMID: 15820304 [PubMed - indexed for MEDLINE]Related articles

    49.

    Dosage balance in gene regulation: biological implications.

    Birchler JA, Riddle NC, Auger DL, Veitia RA.

    Trends Genet. 2005 Apr;21(4):219-26. Review.PMID: 15797617 [PubMed - indexed for MEDLINE]Related articles

    50.

    Gene dosage balance: deletions, duplications and dominance.

    Veitia RA.

    Trends Genet. 2005 Jan;21(1):33-5. No abstract available. PMID: 15680512 [PubMed - indexed for MEDLINE]Related articles

    Supplemental Content

    Filter your results:

    19 free full-text articles in PubMed Central

    Find related data

    Search details

    » See more...

    Recent activity