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Year | Number of Results |
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2010 | 1 |
2014 | 2 |
2022 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 84056
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Common genetic variation in KATNAL1 non-coding regions is involved in the susceptibility to severe phenotypes of male infertility.
Andrology. 2022 Oct;10(7):1339-1350. doi: 10.1111/andr.13221. Epub 2022 Jul 8.
Andrology. 2022.
PMID: 35752927
Free PMC article.
Lack of association of KATNAL1 gene sequence variants and azoospermia in humans.
Fedick AM, Eckert K, Thompson K, Forman EJ, Devkota B, Treff NR, Taylor D, Scott RT Jr.
Fedick AM, et al.
J Assist Reprod Genet. 2014 Aug;31(8):1065-71. doi: 10.1007/s10815-014-0269-1. Epub 2014 Jun 10.
J Assist Reprod Genet. 2014.
PMID: 24913027
Free PMC article.
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A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes.
Bartholdi D, Stray-Pedersen A, Azzarello-Burri S, Kibaek M, Kirchhoff M, Oneda B, Rødningen O, Schmitt-Mechelke T, Rauch A, Kjaergaard S.
Bartholdi D, et al.
Am J Med Genet A. 2014 May;164A(5):1277-83. doi: 10.1002/ajmg.a.36439. Epub 2014 Mar 24.
Am J Med Genet A. 2014.
PMID: 24664804
Free article.
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KL1 is a novel microtubule severing enzyme that regulates mitotic spindle architecture.
Sonbuchner TM, Rath U, Sharp DJ.
Sonbuchner TM, et al.
Cell Cycle. 2010 Jun 15;9(12):2403-11. doi: 10.4161/cc.9.12.11916. Epub 2010 Jun 15.
Cell Cycle. 2010.
PMID: 20519956
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