PubMed (GeneRIF) for id: 84221

Year	Number of Results
2017	2
2018	2
2019	1
2020	1
2021	1
2022	1
2023	1
2024	0

1

Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage.

David D, Fino J, Oliveira R, Dória S, Morton CC. David D, et al. Gene. 2023 Dec 15;887:147737. doi: 10.1016/j.gene.2023.147737. Epub 2023 Aug 23. Gene. 2023. PMID: 37625567 Free article.

2

Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility.

Li YZ, Li N, Liu WS, Sha YW, Wu RF, Tang YL, Zhu XS, Wei XL, Zhang XY, Wang YF, Lu ZX, Zhang FX. Li YZ, et al. Asian J Androl. 2022 Jan-Feb;24(1):67-72. doi: 10.4103/aja.aja_56_21. Asian J Androl. 2022. PMID: 34213489 Free PMC article.

3

PTSD is associated with increased DNA methylation across regions of HLA-DPB1 and SPATC1L.

Katrinli S, Zheng Y, Gautam A, Hammamieh R, Yang R, Venkateswaran S, Kilaru V, Lori A, Hinrichs R, Powers A, Gillespie CF, Wingo AP, Michopoulos V, Jovanovic T, Wolf EJ, McGlinchey RE, Milberg WP, Miller MW, Kugathasan S, Jett M, Logue MW, Ressler KJ, Smith AK. Katrinli S, et al. Brain Behav Immun. 2021 Jan;91:429-436. doi: 10.1016/j.bbi.2020.10.023. Epub 2020 Nov 3. Brain Behav Immun. 2021. PMID: 33152445 Free PMC article.

4

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.

Morgan A, Vuckovic D, Krishnamoorthy N, Rubinato E, Ambrosetti U, Castorina P, Franzè A, Vozzi D, La Bianca M, Cappellani S, Di Stazio M, Gasparini P, Girotto G. Morgan A, et al. Eur J Hum Genet. 2019 Jan;27(1):70-79. doi: 10.1038/s41431-018-0229-9. Epub 2018 Sep 3. Eur J Hum Genet. 2019. PMID: 30177775 Free PMC article.

5

SPATC1L maintains the integrity of the sperm head-tail junction.

Kim J, Kwon JT, Jeong J, Kim J, Hong SH, Kim J, Park ZY, Chung KH, Eddy EM, Cho C. Kim J, et al. EMBO Rep. 2018 Sep;19(9):e45991. doi: 10.15252/embr.201845991. Epub 2018 Jul 19. EMBO Rep. 2018. PMID: 30026308 Free PMC article.

6

Identification of TNFSF13, SPATC1L, SLC22A25 and SALL4 as novel susceptibility loci for atrial fibrillation by an exome‑wide association study.

Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M. Yamada Y, et al. Mol Med Rep. 2017 Nov;16(5):5823-5832. doi: 10.3892/mmr.2017.7334. Epub 2017 Aug 23. Mol Med Rep. 2017. PMID: 28849223 Free PMC article.

7

Identification of EGFLAM, SPATC1L and RNASE13 as novel susceptibility loci for aortic aneurysm in Japanese individuals by exome-wide association studies.

Yamada Y, Sakuma J, Takeuchi I, Yasukochi Y, Kato K, Oguri M, Fujimaki T, Horibe H, Muramatsu M, Sawabe M, Fujiwara Y, Taniguchi Y, Obuchi S, Kawai H, Shinkai S, Mori S, Arai T, Tanaka M. Yamada Y, et al. Int J Mol Med. 2017 May;39(5):1091-1100. doi: 10.3892/ijmm.2017.2927. Epub 2017 Mar 21. Int J Mol Med. 2017. PMID: 28339009 Free PMC article.

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