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Journal Abstract Search

430 related items for PubMed ID: 20184645

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  • 44. Identification of new susceptibility regions for X;Y translocations in patients with testicular disorder of sex development.
    Beaulieu Bergeron M, Lemyre E, Lemieux N.
    Sex Dev; 2011; 5(1):1-6. PubMed ID: 21088380
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  • 45. A study of goat SRY protein expression suggests putative new roles for this gene in the developing testis of a species with long-lasting SRY expression.
    Montazer-Torbati F, Kocer A, Auguste A, Renault L, Charpigny G, Pailhoux E, Pannetier M.
    Dev Dyn; 2010 Dec; 239(12):3324-35. PubMed ID: 20941779
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  • 46. Analysis of SRY gene in 8 cases of sex abnormality.
    Wang H, Teng Y, Tian H, Tang Y, Chen Y, Yang Z.
    J Huazhong Univ Sci Technolog Med Sci; 2004 Dec; 24(5):503-6. PubMed ID: 15641705
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  • 47. [SRY and SOX9: the main genetic factors of mammalian sex determination].
    Kozhukhar' VG.
    Tsitologiia; 2012 Dec; 54(5):390-404. PubMed ID: 22827036
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  • 48. A missense mutation (c.226C>A) in HMG box SRY gene affects nNLS function in 46,XY sex reversal female.
    Ambulkar PS, Waghmare JE, Verma Shivkumar P, Narang P, Pal AK.
    Andrologia; 2021 Jun; 53(5):e14011. PubMed ID: 33570214
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  • 49. A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.
    Klee P, Béna F, Birraux J, Dahoun S, Dirlewanger M, Girardin C, Plotton I, Rougemont AL, Morel Y, Schwitzgebel VM.
    Horm Res Paediatr; 2012 Jun; 78(3):188-92. PubMed ID: 22441105
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  • 50. Analysis of gene function in cultured embryonic mouse gonads using nucleofection.
    Ryan J, Ludbrook L, Wilhelm D, Sinclair A, Koopman P, Bernard P, Harley VR.
    Sex Dev; 2011 Jun; 5(1):7-15. PubMed ID: 21099207
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  • 51. The potential role of SRY in epigenetic gene regulation during brain sexual differentiation in mammals.
    Sekido R.
    Adv Genet; 2014 Jun; 86():135-65. PubMed ID: 25172349
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  • 52. Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.
    McElreavey K, Vilain E, Barbaux S, Fuqua JS, Fechner PY, Souleyreau N, Doco-Fenzy M, Gabriel R, Quereux C, Fellous M, Berkovitz GD.
    Proc Natl Acad Sci U S A; 1996 Aug 06; 93(16):8590-4. PubMed ID: 8710915
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  • 53. An SRY-deleted XXY female resulting from a paternally inherited t(Y;22).
    Kim J, Kim SH, Song J, Choi JR, Kim HS, Lee KA.
    Ann Clin Lab Sci; 2010 Aug 06; 40(3):295-9. PubMed ID: 20689145
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  • 54. XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.
    Maciel-Guerra AT, de Mello MP, Coeli FB, Ribeiro ML, Miranda ML, Marques-de-Faria AP, Baptista MT, Moraes SG, Guerra-Júnior G.
    J Clin Endocrinol Metab; 2008 Feb 06; 93(2):339-43. PubMed ID: 18056774
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  • 55. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report.
    Mutlu GY, Kırmızıbekmez H, Aydın H, Çetiner H, Moralıoğlu S, Celayir AC.
    J Pediatr Endocrinol Metab; 2015 Jan 06; 28(1-2):207-10. PubMed ID: 25153220
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  • 56. Normal female phenotype and ovarian development despite the ovarian expression of the sex-determining region of Y chromosome (SRY) in a 46,XX/69,XXY diploid/triploid mosaic child conceived after in vitro fertilization-intracytoplasmic sperm injection.
    Oktem O, Paduch DA, Xu K, Mielnik A, Oktay K.
    J Clin Endocrinol Metab; 2007 Mar 06; 92(3):1008-14. PubMed ID: 17164312
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  • 57. 46, XX male sex reversal syndrome: a case report and review of the genetic basis.
    Wang T, Liu JH, Yang J, Chen J, Ye ZQ.
    Andrologia; 2009 Feb 06; 41(1):59-62. PubMed ID: 19143733
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  • 58. Equine disorders of sexual development in 17 mares including XX, SRY-negative, XY, SRY-negative and XY, SRY-positive genotypes.
    Villagómez DA, Lear TL, Chenier T, Lee S, McGee RB, Cahill J, Foster RA, Reyes E, St John E, King WA.
    Sex Dev; 2011 Feb 06; 5(1):16-25. PubMed ID: 21196712
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  • 59. Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesis.
    Georg I, Bagheri-Fam S, Knower KC, Wieacker P, Scherer G, Harley VR.
    Sex Dev; 2010 Feb 06; 4(6):321-5. PubMed ID: 20838034
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  • 60. SRY mutation analysis by next generation (deep) sequencing in a cohort of chromosomal Disorders of Sex Development (DSD) patients with a mosaic karyotype.
    Hersmus R, Stoop H, Turbitt E, Oosterhuis JW, Drop SL, Sinclair AH, White SJ, Looijenga LH.
    BMC Med Genet; 2012 Nov 16; 13():108. PubMed ID: 23157850
    [Abstract] [Full Text] [Related]

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