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Year | Number of Results |
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2017 | 1 |
2018 | 2 |
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2024 | 0 |
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Page 1
Pharmacogenomics of human P450 oxidoreductase.
Front Pharmacol. 2014 May 9;5:103. doi: 10.3389/fphar.2014.00103. eCollection 2014.
Front Pharmacol. 2014.
PMID: 24847272
Free PMC article.
Review.
CBX2-dependent transcriptional landscape: implications for human sex development and its defects.
Sproll P, Eid W, Biason-Lauber A.
Sproll P, et al.
Sci Rep. 2019 Nov 12;9(1):16552. doi: 10.1038/s41598-019-53006-7.
Sci Rep. 2019.
PMID: 31719618
Free PMC article.
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The transcriptional regulator CBX2 and ovarian function: A whole genome and whole transcriptome approach.
Bouazzi L, Sproll P, Eid W, Biason-Lauber A.
Bouazzi L, et al. Among authors: sproll p.
Sci Rep. 2019 Nov 19;9(1):17033. doi: 10.1038/s41598-019-53370-4.
Sci Rep. 2019.
PMID: 31745224
Free PMC article.
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Assembling the jigsaw puzzle: CBX2 isoform 2 and its targets in disorders/differences of sex development.
Sproll P, Eid W, Gomes CR, Mendonca BB, Gomes NL, Costa EM, Biason-Lauber A.
Sproll P, et al.
Mol Genet Genomic Med. 2018 Sep;6(5):785-795. doi: 10.1002/mgg3.445. Epub 2018 Jul 11.
Mol Genet Genomic Med. 2018.
PMID: 29998616
Free PMC article.
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Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2).
Lang-Muritano M, Sproll P, Wyss S, Kolly A, Hürlimann R, Konrad D, Biason-Lauber A.
Lang-Muritano M, et al. Among authors: sproll p.
J Clin Endocrinol Metab. 2018 Oct 1;103(10):3748-3756. doi: 10.1210/jc.2018-00769.
J Clin Endocrinol Metab. 2018.
PMID: 30113650
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The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome.
Ilaslan E, Markosyan R, Sproll P, Stevenson BJ, Sajek M, Sajek MP, Hayrapetyan H, Sarkisian T, Livshits L, Nef S, Jaruzelska J, Kusz-Zamelczyk K.
Ilaslan E, et al. Among authors: sproll p.
Int J Mol Sci. 2020 Nov 9;21(21):8403. doi: 10.3390/ijms21218403.
Int J Mol Sci. 2020.
PMID: 33182400
Free PMC article.
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A novel DAX-1 (NR0B1) mutation in a boy with X-linked adrenal hypoplasia congenita.
Gerster K, Katschnig C, Wyss S, Kolly A, Sproll P, Biason-Lauber A, Konrad D.
Gerster K, et al. Among authors: sproll p.
J Pediatr Endocrinol Metab. 2017 Nov 27;30(12):1321-1325. doi: 10.1515/jpem-2017-0261.
J Pediatr Endocrinol Metab. 2017.
PMID: 29087957
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