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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 2
2004 6
2005 8
2006 8
2007 4
2008 9
2009 6
2010 4
2011 3
2012 7
2013 6
2014 10
2015 2
2016 9
2017 13
2018 15
2019 10
2020 11
2021 14
2022 11
2023 9
2024 2

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151 results

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Page 1
POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression.
Cho HJ, Gurbuz F, Stamou M, Kotan LD, Farmer SM, Can S, Tompkins MF, Mammadova J, Altincik SA, Gokce C, Catli G, Bugrul F, Bartlett K, Turan I, Balasubramanian R, Yuksel B, Seminara SB, Wray S, Topaloglu AK. Cho HJ, et al. Front Endocrinol (Lausanne). 2023 Aug 1;14:1203542. doi: 10.3389/fendo.2023.1203542. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37600690 Free PMC article.
Exosome Precipitation by Ionic Strength Modulation: ExoPRISM.
Sunkara V, Park J, Han J, Del Río JS, Cho HJ, Oh IJ, Cho YK. Sunkara V, et al. Among authors: cho hj. ACS Appl Mater Interfaces. 2023 Nov 28;15(49):56807-19. doi: 10.1021/acsami.3c13527. Online ahead of print. ACS Appl Mater Interfaces. 2023. PMID: 38017017 Free PMC article.
PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadism.
Welch BA, Cho HJ, Ucakturk SA, Farmer SM, Cetinkaya S, Abaci A, Akkus G, Simsek E, Kotan LD, Turan I, Gurbuz F, Yuksel B, Wray S, Topaloglu AK. Welch BA, et al. Among authors: cho hj. J Neuroendocrinol. 2022 Apr;34(4):e13103. doi: 10.1111/jne.13103. Epub 2022 Feb 16. J Neuroendocrinol. 2022. PMID: 35170806 Free PMC article.
151 results