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Year Number of Results
2006 2
2007 1
2008 1
2009 2
2010 3
2015 1
2016 3
2020 3
2021 1
2022 5
2023 1
2024 1

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24 results

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Page 1
Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility.
Cerván-Martín M, Tüttelmann F, Lopes AM, Bossini-Castillo L, Rivera-Egea R, Garrido N, Lujan S, Romeu G, Santos-Ribeiro S, Castilla JA, Carmen Gonzalvo M, Clavero A, Maldonado V, Vicente FJ, González-Muñoz S, Guzmán-Jiménez A, Burgos M, Jiménez R, Pacheco A, González C, Gómez S, Amorós D, Aguilar J, Quintana F, Calhaz-Jorge C, Aguiar A, Nunes J, Sousa S, Pereira I, Pinto MG, Correia S, Sánchez-Curbelo J, López-Rodrigo O, Martín J, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Gromoll J, Bassas L, Seixas S, Gonçalves J, Larriba S, Kliesch S, Palomino-Morales RJ, Carmona FD. Cerván-Martín M, et al. Among authors: palomino morales rj. Commun Biol. 2022 Nov 10;5(1):1220. doi: 10.1038/s42003-022-04192-0. Commun Biol. 2022. PMID: 36357561 Free PMC article.
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels.
Schubert M, Pérez Lanuza L, Wöste M, Dugas M, Carmona FD, Palomino-Morales RJ, Rassam Y, Heilmann-Heimbach S, Tüttelmann F, Kliesch S, Gromoll J. Schubert M, et al. Among authors: palomino morales rj. J Clin Endocrinol Metab. 2022 Jul 14;107(8):2350-2361. doi: 10.1210/clinem/dgac165. J Clin Endocrinol Metab. 2022. PMID: 35305013 Free PMC article.
Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia.
Guzmán-Jiménez A, González-Muñoz S, Cerván-Martín M, Rivera-Egea R, Garrido N, Luján S, Santos-Ribeiro S, Castilla JA, Gonzalvo MC, Clavero A, Vicente FJ, Maldonado V, Villegas-Salmerón J, Burgos M, Jiménez R, Pinto MG, Pereira I, Nunes J, Sánchez-Curbelo J, López-Rodrigo O, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Lopes AM, Larriba S, Palomino-Morales RJ, Carmona FD, Bossini-Castillo L; IVIRMA Group; Lisbon Clinical Group. Guzmán-Jiménez A, et al. Among authors: palomino morales rj. Front Cell Dev Biol. 2022 Dec 15;10:1089782. doi: 10.3389/fcell.2022.1089782. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36589743 Free PMC article.
Sex-specific association of SELL gene polymorphisms with pattern hair loss in the Thai population: A candidate gene association study and in silico functional characterization.
Khantham C, Ruksiriwanich W, Chaitep T, Linsaenkart P, Muangsanguan A, Guzmán-Jiménez A, Cerván-Martín M, Bossini-Castillo L, Gonzalez-Muñoz S, Palomino-Morales RJ, Leetrakool N, Shaengkhamnang B, Chittasupho C, Jantrawut P, Sommano SR, Phimolsiripol Y, Carmona FD. Khantham C, et al. Among authors: palomino morales rj. J Dermatol Sci. 2023 Feb;109(2):102-105. doi: 10.1016/j.jdermsci.2023.02.003. Epub 2023 Feb 14. J Dermatol Sci. 2023. PMID: 36828746 No abstract available.
Prognosis Relevance of Serum Cytokines in Pancreatic Cancer.
Torres C, Linares A, Alejandre MJ, Palomino-Morales RJ, Caba O, Prados J, Aránega A, Delgado JR, Irigoyen A, Martínez-Galán J, Ortuño FM, Rojas I, Perales S. Torres C, et al. Among authors: palomino morales rj. Biomed Res Int. 2015;2015:518284. doi: 10.1155/2015/518284. Epub 2015 Aug 4. Biomed Res Int. 2015. PMID: 26346854 Free PMC article. Clinical Trial.
Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome.
Cerván-Martín M, Bossini-Castillo L, Guzmán-Jimenez A, Rivera-Egea R, Garrido N, Luján S, Romeu G, Santos-Ribeiro S, Ivirma Group, Lisbon Clinical Group, Castilla JA, Gonzalvo MC, Clavero A, Vicente FJ, Maldonado V, González-Muñoz S, Rodríguez-Martín I, Burgos M, Jiménez R, Pinto MG, Pereira I, Nunes J, Sánchez-Curbelo J, López-Rodrigo O, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Larriba S, Lopes AM, Carmona FD, Palomino-Morales RJ. Cerván-Martín M, et al. Among authors: palomino morales rj. J Pers Med. 2022 Jun 4;12(6):932. doi: 10.3390/jpm12060932. J Pers Med. 2022. PMID: 35743717 Free PMC article.
Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment.
Cerván-Martín M, Suazo-Sánchez MI, Rivera-Egea R, Garrido N, Luján S, Romeu G, Santos-Ribeiro S, Castilla JA, Gonzalvo MC, Clavero A, Vicente FJ, Maldonado V, Burgos M, Barrionuevo FJ, Jiménez R, Sánchez-Curbelo J, López-Rodrigo O, Peraza MF, Pereira-Caetano I, Marques PI, Carvalho F, Barros A, Bassas L, Seixas S, Gonçalves J, Larriba S, Lopes AM, Palomino-Morales RJ, Carmona FD; Lisbon Clinical Group; IVIRMA Group. Cerván-Martín M, et al. Among authors: palomino morales rj. Fertil Steril. 2020 Aug;114(2):398-406. doi: 10.1016/j.fertnstert.2020.02.115. Epub 2020 Jul 18. Fertil Steril. 2020. PMID: 32690270 Free article.
24 results