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Items: 1 to 50 of 153

1.

The Gene Balance Hypothesis: Epigenetics and Dosage Effects in Plants.

Shi X, Chen C, Yang H, Hou J, Ji T, Cheng J, Veitia RA, Birchler JA.

Methods Mol Biol. 2020;2093:161-171. doi: 10.1007/978-1-0716-0179-2_12.

PMID:
32088896
2.

Special issue on "Molecular genetics of aging and longevity": a critical time in the field of geroscience.

Benayoun BA, Veitia RA.

Hum Genet. 2020 Mar;139(3):275-276. doi: 10.1007/s00439-020-02125-7. No abstract available.

PMID:
32052140
3.

Conventional and unconventional interactions of the transcription factor FOXL2 uncovered by a proteome-wide analysis.

Penrad-Mobayed M, Perrin C, Herman L, Todeschini AL, Nigon F, Cosson B, Caburet S, Veitia RA.

FASEB J. 2020 Jan;34(1):571-587. doi: 10.1096/fj.201901573R. Epub 2019 Nov 25.

PMID:
31914586
4.

MIRAGE Syndrome: Phenotypic Rescue by Somatic Mutation and Selection.

Veitia RA.

Trends Mol Med. 2019 Nov;25(11):937-940. doi: 10.1016/j.molmed.2019.08.008. Epub 2019 Oct 14.

PMID:
31624021
5.

DNA Content, Cell Size, and Cell Senescence.

Veitia RA.

Trends Biochem Sci. 2019 Aug;44(8):645-647. doi: 10.1016/j.tibs.2019.04.013. Epub 2019 May 31.

PMID:
31160123
6.

Causes and effects of haploinsufficiency.

Johnson AF, Nguyen HT, Veitia RA.

Biol Rev Camb Philos Soc. 2019 Oct;94(5):1774-1785. doi: 10.1111/brv.12527. Epub 2019 May 31.

PMID:
31149781
7.

Insights into the loss of the Y chromosome with age in control individuals and in patients with age-related macular degeneration using genotyping microarray data.

Grassmann F; International AMD Genomics Consortium (IAMDGC), Weber BHF, Veitia RA.

Hum Genet. 2020 Mar;139(3):401-407. doi: 10.1007/s00439-019-02029-1. Epub 2019 May 27.

PMID:
31134332
8.

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

Caburet S, Todeschini AL, Petrillo C, Martini E, Farran ND, Legois B, Livera G, Younis JS, Shalev S, Veitia RA.

EBioMedicine. 2019 Apr;42:524-531. doi: 10.1016/j.ebiom.2019.03.075. Epub 2019 Apr 15.

9.

High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells.

Elzaiat M, Herman L, Legois B, Léger T, Todeschini AL, Veitia RA.

Mol Cell Proteomics. 2019 Jul;18(7):1307-1319. doi: 10.1074/mcp.RA119.001461. Epub 2019 Apr 16.

PMID:
30992313
10.

Genomic Balance and Speciation.

Birchler JA, Veitia RA.

Epigenet Insights. 2019 Mar 31;12:2516865719840291. doi: 10.1177/2516865719840291. eCollection 2019.

11.

Darwinian selection within an individual or somatic selection: facts and models.

Veitia RA.

J Mol Cell Biol. 2019 Aug 19;11(8):719-722. doi: 10.1093/jmcb/mjz014. No abstract available.

12.

Further quantitative insights into the decrease of heteroplasmy of m.3243A>G with age in leukocytes.

Veitia RA.

Clin Genet. 2019 Apr;95(4):542-543. doi: 10.1111/cge.13496. Epub 2019 Jan 28. No abstract available.

PMID:
30690711
13.

AFF3: a new player in maintaining XIST monoallelic expression.

Veitia RA.

J Mol Cell Biol. 2019 Sep 19;11(9):723-724. doi: 10.1093/jmcb/mjy082. No abstract available.

14.

On the loss of human sex chromosomes in lymphocytes with age: a quantitative treatment.

Veitia RA.

Eur J Hum Genet. 2018 Dec;26(12):1875-1878. doi: 10.1038/s41431-018-0225-0. Epub 2018 Aug 10.

16.

A role for SOX9 in post-transcriptional processes: insights from the amphibian oocyte.

Penrad-Mobayed M, Perrin C, L'Hôte D, Contremoulins V, Lepesant JA, Boizet-Bonhoure B, Poulat F, Baudin X, Veitia RA.

Sci Rep. 2018 May 8;8(1):7191. doi: 10.1038/s41598-018-25356-1.

17.

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency.

Huhtaniemi I, Hovatta O, La Marca A, Livera G, Monniaux D, Persani L, Heddar A, Jarzabek K, Laisk-Podar T, Salumets A, Tapanainen JS, Veitia RA, Visser JA, Wieacker P, Wolczynski S, Misrahi M.

Trends Endocrinol Metab. 2018 Jun;29(6):400-419. doi: 10.1016/j.tem.2018.03.010. Epub 2018 Apr 26. Review.

18.

How the most common mitochondrial DNA mutation (m.3243A>G) vanishes from leukocytes: a mathematical model.

Veitia RA.

Hum Mol Genet. 2018 May 1;27(9):1565-1571. doi: 10.1093/hmg/ddy063.

PMID:
29474538
19.

Natural and molecular history of prolactinoma: insights from a Prlr-/- mouse model.

Bernard V, Villa C, Auguste A, Lamothe S, Guillou A, Martin A, Caburet S, Young J, Veitia RA, Binart N.

Oncotarget. 2017 Dec 27;9(5):6144-6155. doi: 10.18632/oncotarget.23713. eCollection 2018 Jan 19.

20.

Gene Expression Dominance in Allopolyploids: Hypotheses and Models.

Bottani S, Zabet NR, Wendel JF, Veitia RA.

Trends Plant Sci. 2018 May;23(5):393-402. doi: 10.1016/j.tplants.2018.01.002. Epub 2018 Feb 9. Review.

PMID:
29433919
21.

Three-dimensional genome architecture in health and disease.

Ouimette JF, Rougeulle C, Veitia RA.

Clin Genet. 2019 Feb;95(2):189-198. doi: 10.1111/cge.13219. Epub 2018 Mar 2. Review.

PMID:
29377081
22.

A homozygous FANCM mutation underlies a familial case of non-syndromic primary ovarian insufficiency.

Fouquet B, Pawlikowska P, Caburet S, Guigon C, Mäkinen M, Tanner L, Hietala M, Urbanska K, Bellutti L, Legois B, Bessieres B, Gougeon A, Benachi A, Livera G, Rosselli F, Veitia RA, Misrahi M.

Elife. 2017 Dec 12;6. pii: e30490. doi: 10.7554/eLife.30490.

23.

Gene Duplicates: Agents of Fragility? - A Reply to Landry and Diss.

Veitia RA.

Trends Genet. 2017 Oct;33(10):658-660. doi: 10.1016/j.tig.2017.07.013. Epub 2017 Aug 17. No abstract available.

PMID:
28823576
24.

Mechanisms of Mendelian dominance.

Veitia RA, Caburet S, Birchler JA.

Clin Genet. 2018 Mar;93(3):419-428. doi: 10.1111/cge.13107. Epub 2017 Oct 26. Review.

PMID:
28755412
25.

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.

Paris F, Flatters D, Caburet S, Legois B, Servant N, Lefebvre H, Sultan C, Veitia RA.

Clin Endocrinol (Oxf). 2017 Nov;87(5):539-544. doi: 10.1111/cen.13420. Epub 2017 Aug 13.

PMID:
28708305
26.

A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.

Carlosama C, Elzaiat M, Patiño LC, Mateus HE, Veitia RA, Laissue P.

Hum Mol Genet. 2017 Aug 15;26(16):3161-3166. doi: 10.1093/hmg/ddx199.

PMID:
28541421
27.

Gene Duplicates: Agents of Robustness or Fragility?

Veitia RA.

Trends Genet. 2017 Jun;33(6):377-379. doi: 10.1016/j.tig.2017.03.006. Epub 2017 Apr 20.

PMID:
28434610
28.

A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome.

Caburet S, Fruchter RB, Legois B, Fellous M, Shalev S, Veitia RA.

Eur J Endocrinol. 2017 May;176(5):K9-K14. doi: 10.1530/EJE-16-0968.

PMID:
28348023
29.

Aging: Somatic Mutations, Epigenetic Drift and Gene Dosage Imbalance.

Veitia RA, Govindaraju DR, Bottani S, Birchler JA.

Trends Cell Biol. 2017 Apr;27(4):299-310. doi: 10.1016/j.tcb.2016.11.006. Epub 2016 Dec 9. Review.

PMID:
27939088
30.

A Fresh Look at 'Aging' Proteins.

Veitia RA.

Trends Biochem Sci. 2017 Feb;42(2):86-89. doi: 10.1016/j.tibs.2016.11.001. Epub 2016 Nov 14.

PMID:
27856135
31.

Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans.

Laissue P, Lakhal B, Vatin M, Batista F, Burgio G, Mercier E, Santos ED, Buffat C, Sierra-Diaz DC, Renault G, Montagutelli X, Salmon J, Monget P, Veitia RA, Méhats C, Fellous M, Gris JC, Cocquet J, Vaiman D.

Open Biol. 2016 Oct;6(10). pii: 160109.

32.

The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2.

Elzaiat M, Todeschini AL, Caburet S, Veitia RA.

Clin Genet. 2017 Feb;91(2):173-182. doi: 10.1111/cge.12862. Epub 2016 Sep 29. Review.

PMID:
27604691
33.

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.

Bouilly J, Beau I, Barraud S, Bernard V, Azibi K, Fagart J, Fèvre A, Todeschini AL, Veitia RA, Beldjord C, Delemer B, Dodé C, Young J, Binart N.

J Clin Endocrinol Metab. 2016 Dec;101(12):4541-4550. Epub 2016 Sep 7.

PMID:
27603904
34.

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.

Baetens D, Stoop H, Peelman F, Todeschini AL, Rosseel T, Coppieters F, Veitia RA, Looijenga LH, De Baere E, Cools M.

Genet Med. 2017 Apr;19(4):367-376. doi: 10.1038/gim.2016.118. Epub 2016 Aug 4.

35.

Hill function-based models of transcriptional switches: impact of specific, nonspecific, functional and nonfunctional binding.

Bottani S, Veitia RA.

Biol Rev Camb Philos Soc. 2017 May;92(2):953-963. doi: 10.1111/brv.12262. Epub 2016 Apr 8.

PMID:
27061969
36.

Kinetics genetics: Incorporating the concept of genomic balance into an understanding of quantitative traits.

Birchler JA, Johnson AF, Veitia RA.

Plant Sci. 2016 Apr;245:128-34. doi: 10.1016/j.plantsci.2016.02.002. Epub 2016 Feb 6. Review.

PMID:
26940497
37.

A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.

Fauchereau F, Shalev S, Chervinsky E, Beck-Fruchter R, Legois B, Fellous M, Caburet S, Veitia RA.

Clin Genet. 2016 May;89(5):603-7. doi: 10.1111/cge.12736. Epub 2016 Feb 10.

PMID:
26771056
38.

Clinical Genetics in the age of Genomics and Genome editing.

Veitia RA.

Clin Genet. 2016 Jan;89(1):3-4. doi: 10.1111/cge.12689. No abstract available.

PMID:
26768808
39.

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Auguste A, Bessière L, Todeschini AL, Caburet S, Sarnacki S, Prat J, D'angelo E, De La Grange P, Ariste O, Lemoine F, Legois B, Sultan C, Zider A, Galmiche L, Kalfa N, Veitia RA.

Hum Mol Genet. 2015 Dec 1;24(23):6687-98. doi: 10.1093/hmg/ddv373. Epub 2015 Sep 11.

PMID:
26362254
40.

Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1.

Coppieters F, Todeschini AL, Fujimaki T, Baert A, De Bruyne M, Van Cauwenbergh C, Verdin H, Bauwens M, Ongenaert M, Kondo M, Meire F, Murakami A, Veitia RA, Leroy BP, De Baere E.

Hum Mutat. 2015 Dec;36(12):1188-96. doi: 10.1002/humu.22899. Epub 2015 Oct 1.

41.

Models of buffering of dosage imbalances in protein complexes.

Veitia RA, Birchler JA.

Biol Direct. 2015 Aug 15;10:42. doi: 10.1186/s13062-015-0063-8.

42.

A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors.

Bessière L, Todeschini AL, Auguste A, Sarnacki S, Flatters D, Legois B, Sultan C, Kalfa N, Galmiche L, Veitia RA.

EBioMedicine. 2015 Mar 6;2(5):421-31. doi: 10.1016/j.ebiom.2015.03.002. eCollection 2015 May.

43.

Gene dosage imbalances: action, reaction, and models.

Veitia RA, Potier MC.

Trends Biochem Sci. 2015 Jun;40(6):309-17. doi: 10.1016/j.tibs.2015.03.011. Epub 2015 Apr 27. Review.

PMID:
25937627
44.

Synthetic lethals in HIV: ways to avoid drug resistance : Running title: Preventing HIV resistance.

Petitjean M, Badel A, Veitia RA, Vanet A.

Biol Direct. 2015 Apr 17;10:17. doi: 10.1186/s13062-015-0044-y.

45.

Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes.

Caburet S, Anttonen M, Todeschini AL, Unkila-Kallio L, Mestivier D, Butzow R, Veitia RA.

BMC Cancer. 2015 Apr 10;15:251. doi: 10.1186/s12885-015-1283-0.

46.

X chromosome inactivation and active X upregulation in therian mammals: facts, questions, and hypotheses.

Veitia RA, Veyrunes F, Bottani S, Birchler JA.

J Mol Cell Biol. 2015 Feb;7(1):2-11. doi: 10.1093/jmcb/mjv001. Epub 2015 Jan 6. Review.

PMID:
25564545
47.

The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells.

Georges A, L'Hôte D, Todeschini AL, Auguste A, Legois B, Zider A, Veitia RA.

Elife. 2014 Nov 4;3. doi: 10.7554/eLife.04207.

48.

Transcription factors: specific DNA binding and specific gene regulation.

Todeschini AL, Georges A, Veitia RA.

Trends Genet. 2014 Jun;30(6):211-9. doi: 10.1016/j.tig.2014.04.002. Epub 2014 Apr 26. Review.

PMID:
24774859
49.

NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis.

Bouilly J, Veitia RA, Binart N.

J Mol Cell Biol. 2014 Apr;6(2):175-7. doi: 10.1093/jmcb/mju006. Epub 2014 Mar 11. No abstract available.

PMID:
24620032
50.

STAG3 is a strong candidate gene for male infertility.

Llano E, Gomez-H L, García-Tuñón I, Sánchez-Martín M, Caburet S, Barbero JL, Schimenti JC, Veitia RA, Pendas AM.

Hum Mol Genet. 2014 Jul 1;23(13):3421-31. doi: 10.1093/hmg/ddu051. Epub 2014 Mar 7.

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