These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

306 related articles for article (PubMed ID: 19849982)

  • 1. [NR5A1 and ovarian failure].
    Bashamboo A; Ravel C; Brauner R; McElreavey K
    Med Sci (Paris); 2009 Oct; 25(10):809-13. PubMed ID: 19849982
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Limited contribution of NR5A1 (SF-1) mutations in women with primary ovarian insufficiency (POI).
    Janse F; de With LM; Duran KJ; Kloosterman WP; Goverde AJ; Lambalk CB; Laven JS; Fauser BC; Giltay JC;
    Fertil Steril; 2012 Jan; 97(1):141-6.e2. PubMed ID: 22100173
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals.
    Camats N; Pandey AV; Fernández-Cancio M; Andaluz P; Janner M; Torán N; Moreno F; Bereket A; Akcay T; García-García E; Muñoz MT; Gracia R; Nistal M; Castaño L; Mullis PE; Carrascosa A; Audí L; Flück CE
    J Clin Endocrinol Metab; 2012 Jul; 97(7):E1294-306. PubMed ID: 22549935
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NR5A1/SF-1 and development and function of the ovary.
    Bashamboo A; McElreavey K
    Ann Endocrinol (Paris); 2010 May; 71(3):177-82. PubMed ID: 20394914
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Wide spectrum of NR5A1-related phenotypes in 46,XY and 46,XX individuals.
    Domenice S; Machado AZ; Ferreira FM; Ferraz-de-Souza B; Lerario AM; Lin L; Nishi MY; Gomes NL; da Silva TE; Silva RB; Correa RV; Montenegro LR; Narciso A; Costa EM; Achermann JC; Mendonca BB
    Birth Defects Res C Embryo Today; 2016 Dec; 108(4):309-320. PubMed ID: 28033660
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression.
    Suwanai AS; Ishii T; Haruna H; Yamataka A; Narumi S; Fukuzawa R; Ogata T; Hasegawa T
    Clin Endocrinol (Oxf); 2013 Jun; 78(6):957-65. PubMed ID: 23095176
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in NR5A1 associated with ovarian insufficiency.
    Lourenço D; Brauner R; Lin L; De Perdigo A; Weryha G; Muresan M; Boudjenah R; Guerra-Junior G; Maciel-Guerra AT; Achermann JC; McElreavey K; Bashamboo A
    N Engl J Med; 2009 Mar; 360(12):1200-10. PubMed ID: 19246354
    [TBL] [Abstract][Full Text] [Related]  

  • 8. NR5A1 (SF-1) mutations are not a major cause of primary ovarian insufficiency.
    Voican A; Bachelot A; Bouligand J; Francou B; Dulon J; Lombès M; Touraine P; Guiochon-Mantel A
    J Clin Endocrinol Metab; 2013 May; 98(5):E1017-21. PubMed ID: 23543655
    [TBL] [Abstract][Full Text] [Related]  

  • 9. NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency.
    Philibert P; Paris F; Lakhal B; Audran F; Gaspari L; Saâd A; Christin-Maître S; Bouchard P; Sultan C
    Fertil Steril; 2013 Feb; 99(2):484-9. PubMed ID: 23153500
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure.
    Harrison SM; Campbell IM; Keays M; Granberg CF; Villanueva C; Tannin G; Zinn AR; Castrillon DH; Shaw CA; Stankiewicz P; Baker LA
    Am J Med Genet A; 2013 Oct; 161A(10):2487-94. PubMed ID: 23918653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.
    Bertrand-Delepine J; Manouvrier-Hanu S; Cartigny M; Paris F; Mallet D; Philibert P; Morel Y; Lefevre C; Dewailly D; Catteau-Jonard S
    Reprod Biomed Online; 2020 Jan; 40(1):151-159. PubMed ID: 31831369
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility.
    Jaillard S; Sreenivasan R; Beaumont M; Robevska G; Dubourg C; Knarston IM; Akloul L; van den Bergen J; Odent S; Croft B; Jouve G; Grover SR; Duros S; Pimentel C; Belaud-Rotureau MA; Ayers KL; Ravel C; Tucker EJ; Sinclair AH
    Maturitas; 2020 Jan; 131():78-86. PubMed ID: 31787151
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation.
    Safari S; Zare-Abdollahi D; Mirfakhraie R; Ghafouri-Fard S; Pouresmaeili F; Movafagh A; Omrani MD
    Climacteric; 2014 Jun; 17(3):301-3. PubMed ID: 24067197
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.
    Bouhali K; Dipietromaria A; Fontaine A; Caburet S; Barbieri O; Bellessort B; Fellous M; Veitia RA; Levi G
    Hum Mol Genet; 2011 Jul; 20(13):2642-50. PubMed ID: 21505076
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development.
    Bashamboo A; Donohoue PA; Vilain E; Rojo S; Calvel P; Seneviratne SN; Buonocore F; Barseghyan H; Bingham N; Rosenfeld JA; Mulukutla SN; Jain M; Burrage L; Dhar S; Balasubramanyam A; Lee B; ; Dumargne MC; Eozenou C; Suntharalingham JP; de Silva K; Lin L; Bignon-Topalovic J; Poulat F; Lagos CF; McElreavey K; Achermann JC
    Hum Mol Genet; 2016 Aug; 25(16):3446-3453. PubMed ID: 27378692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency.
    Fabbri HC; de Andrade JG; Soardi FC; de Calais FL; Petroli RJ; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
    BMC Med Genet; 2014 Jan; 15():7. PubMed ID: 24405868
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Update--steroidogenic factor 1 (SF-1, NR5A1).
    Köhler B; Achermann JC
    Minerva Endocrinol; 2010 Jun; 35(2):73-86. PubMed ID: 20595937
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1-mutated patient's management.
    Colson C; Aubry E; Cartigny M; Rémy AA; Franquet H; Leroy X; Kéchid G; Lefèvre C; Besson R; Cools M; Spinoit AF; Sultan C; Manouvrier S; Philibert P; Ghoumid J
    Clin Genet; 2017 Jul; 92(1):99-103. PubMed ID: 28032338
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three new SF-1 (NR5A1) gene mutations in two unrelated families with multiple affected members: within-family variability in 46,XY subjects and low ovarian reserve in fertile 46,XX subjects.
    Warman DM; Costanzo M; Marino R; Berensztein E; Galeano J; Ramirez PC; Saraco N; Baquedano MS; Ciaccio M; Guercio G; Chaler E; Maceiras M; Lazzatti JM; Bailez M; Rivarola MA; Belgorosky A
    Horm Res Paediatr; 2011; 75(1):70-7. PubMed ID: 20861607
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Partial deletion of the NR5A1 (SF1) gene detected by synthetic probe MLPA in a patient with XY gonadal disorder of sex development.
    Barbaro M; Cools M; Looijenga LH; Drop SL; Wedell A
    Sex Dev; 2011; 5(4):181-7. PubMed ID: 21654157
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.