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

Year Number of Results
1984 1
1988 3
1990 1
1991 1
1992 1
1994 1
1997 1
2011 2
2012 2
2013 3
2014 2
2015 4
2016 2
2017 2
2019 2
2020 3
2021 4
2022 2
2023 1
2024 0

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35 results

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Page 1
Development of the Pituitary Gland.
Alatzoglou KS, Gregory LC, Dattani MT. Alatzoglou KS, et al. Among authors: gregory lc. Compr Physiol. 2020 Mar 12;10(2):389-413. doi: 10.1002/cphy.c150043. Compr Physiol. 2020. PMID: 32163208 Review.
Pituitary gland development: an update.
Bancalari RE, Gregory LC, McCabe MJ, Dattani MT. Bancalari RE, et al. Among authors: gregory lc. Endocr Dev. 2012;23:1-15. doi: 10.1159/000341733. Epub 2012 Nov 23. Endocr Dev. 2012. PMID: 23182816 Review.
Manufacture of measles viruses.
Langfield KK, Walker HJ, Gregory LC, Federspiel MJ. Langfield KK, et al. Among authors: gregory lc. Methods Mol Biol. 2011;737:345-66. doi: 10.1007/978-1-61779-095-9_14. Methods Mol Biol. 2011. PMID: 21590404
Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism.
Hietamäki J, Gregory LC, Ayoub S, Iivonen AP, Vaaralahti K, Liu X, Brandstack N, Buckton AJ, Laine T, Känsäkoski J, Hero M, Miettinen PJ, Varjosalo M, Wakeling E, Dattani MT, Raivio T. Hietamäki J, et al. Among authors: gregory lc. J Clin Endocrinol Metab. 2020 Jun 1;105(6):1748-58. doi: 10.1210/clinem/dgaa078. J Clin Endocrinol Metab. 2020. PMID: 32060556 Free PMC article.
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.
Akin L, Rizzoti K, Gregory LC, Corredor B, Le Quesne Stabej P, Williams H, Buonocore F, Mouilleron S, Capra V, McGlacken-Byrne SM, Martos-Moreno GÁ, Azmanov DN, Kendirci M, Kurtoglu S, Suntharalingham JP, Galichet C, Gustincich S, Tasic V, Achermann JC, Accogli A, Filipovska A, Tuilpakov A, Maghnie M, Gucev Z, Gonen ZB, Pérez-Jurado LA, Robinson I, Lovell-Badge R, Argente J, Dattani MT. Akin L, et al. Among authors: gregory lc. Genet Med. 2022 Feb;24(2):384-397. doi: 10.1016/j.gim.2021.09.019. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906446 Free PMC article.
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia.
Whittaker DE, Oleari R, Gregory LC, Le Quesne-Stabej P, Williams HJ; GOSgene; Torpiano JG, Formosa N, Cachia MJ, Field D, Lettieri A, Ocaka LA, Paganoni AJ, Rajabali SH, Riegman KL, De Martini LB, Chaya T, Robinson IC, Furukawa T, Cariboni A, Basson MA, Dattani MT. Whittaker DE, et al. Among authors: gregory lc. J Clin Invest. 2021 Dec 15;131(24):e141587. doi: 10.1172/JCI141587. J Clin Invest. 2021. PMID: 34730112 Free PMC article.
The phenotypic spectrum associated with OTX2 mutations in humans.
Gregory LC, Gergics P, Nakaguma M, Bando H, Patti G, McCabe MJ, Fang Q, Ma Q, Ozel AB, Li JZ, Poina MM, Jorge AAL, Benedetti AFF, Lerario AM, Arnhold IJP, Mendonca BB, Maghnie M, Camper SA, Carvalho LRS, Dattani MT. Gregory LC, et al. Eur J Endocrinol. 2021 May 25;185(1):121-135. doi: 10.1530/EJE-20-1453. Eur J Endocrinol. 2021. PMID: 33950863 Free PMC article.
35 results