Sort by
Items per page

Send to

Choose Destination

Links from Gene

Items: 1 to 20 of 35


Repair of exogenous DNA double-strand breaks promotes chromosome synapsis in SPO11-mutant mouse meiocytes, and is altered in the absence of HORMAD1.

Carofiglio F, Sleddens-Linkels E, Wassenaar E, Inagaki A, van Cappellen WA, Grootegoed JA, Toth A, Baarends WM.

DNA Repair (Amst). 2018 Mar;63:25-38. doi: 10.1016/j.dnarep.2018.01.007. Epub 2018 Jan 31.


A novel mammalian HORMA domain-containing protein, HORMAD1, preferentially associates with unsynapsed meiotic chromosomes.

Fukuda T, Daniel K, Wojtasz L, Toth A, Höög C.

Exp Cell Res. 2010 Jan 15;316(2):158-71. doi: 10.1016/j.yexcr.2009.08.007. Epub 2009 Aug 15.


Restricted germ cell expression of a gene encoding a novel mammalian HORMA domain-containing protein.

Pangas SA, Yan W, Matzuk MM, Rajkovic A.

Gene Expr Patterns. 2004 Dec;5(2):257-63.


Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion.

Winters T, McNicoll F, Jessberger R.

EMBO J. 2014 Jun 2;33(11):1256-70. doi: 10.1002/embj.201387330. Epub 2014 May 5.


Meiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in mice.

Stanzione M, Baumann M, Papanikos F, Dereli I, Lange J, Ramlal A, Tränkner D, Shibuya H, de Massy B, Watanabe Y, Jasin M, Keeney S, Tóth A.

Nat Cell Biol. 2016 Nov;18(11):1208-1220. doi: 10.1038/ncb3417. Epub 2016 Oct 10.


MEI4 – a central player in the regulation of meiotic DNA double-strand break formation in the mouse.

Kumar R, Ghyselinck N, Ishiguro K, Watanabe Y, Kouznetsova A, Höög C, Strong E, Schimenti J, Daniel K, Toth A, de Massy B.

J Cell Sci. 2015 May 1;128(9):1800-11. doi: 10.1242/jcs.165464. Epub 2015 Mar 20.


Mouse HORMAD1 and HORMAD2, two conserved meiotic chromosomal proteins, are depleted from synapsed chromosome axes with the help of TRIP13 AAA-ATPase.

Wojtasz L, Daniel K, Roig I, Bolcun-Filas E, Xu H, Boonsanay V, Eckmann CR, Cooke HJ, Jasin M, Keeney S, McKay MJ, Toth A.

PLoS Genet. 2009 Oct;5(10):e1000702. doi: 10.1371/journal.pgen.1000702. Epub 2009 Oct 23.


Meiotic DNA double-strand breaks and chromosome asynapsis in mice are monitored by distinct HORMAD2-independent and -dependent mechanisms.

Wojtasz L, Cloutier JM, Baumann M, Daniel K, Varga J, Fu J, Anastassiadis K, Stewart AF, Reményi A, Turner JM, Tóth A.

Genes Dev. 2012 May 1;26(9):958-73. doi: 10.1101/gad.187559.112.


Phosphorylation of chromosome core components may serve as axis marks for the status of chromosomal events during mammalian meiosis.

Fukuda T, Pratto F, Schimenti JC, Turner JM, Camerini-Otero RD, Höög C.

PLoS Genet. 2012 Feb;8(2):e1002485. doi: 10.1371/journal.pgen.1002485. Epub 2012 Feb 9.


Transcription factors SOHLH1 and SOHLH2 coordinate oocyte differentiation without affecting meiosis I.

Shin YH, Ren Y, Suzuki H, Golnoski KJ, Ahn HW, Mico V, Rajkovic A.

J Clin Invest. 2017 Jun 1;127(6):2106-2117. doi: 10.1172/JCI90281. Epub 2017 May 15.


Hormad1 mutation disrupts synaptonemal complex formation, recombination, and chromosome segregation in mammalian meiosis.

Shin YH, Choi Y, Erdin SU, Yatsenko SA, Kloc M, Yang F, Wang PJ, Meistrich ML, Rajkovic A.

PLoS Genet. 2010 Nov 4;6(11):e1001190. doi: 10.1371/journal.pgen.1001190. Erratum in: PLoS Genet. 2011;7(2). doi: 10.1371/annotation/8aa656b6-55f7-4795-a441-cf243ea62175.


Evolutionarily-conserved MZIP2 is essential for crossover formation in mammalian meiosis.

Zhang Q, Shao J, Fan HY, Yu C.

Commun Biol. 2018 Sep 21;1:147. doi: 10.1038/s42003-018-0154-z. eCollection 2018.


Loss of Glis3 causes dysregulation of retrotransposon silencing and germ cell demise in fetal mouse testis.

Ungewitter EK, Rotgers E, Kang HS, Lichti-Kaiser K, Li L, Grimm SA, Jetten AM, Yao HH.

Sci Rep. 2018 Jun 25;8(1):9662. doi: 10.1038/s41598-018-27843-x.


MORC2B is essential for meiotic progression and fertility.

Shi B, Xue J, Zhou J, Kasowitz SD, Zhang Y, Liang G, Guan Y, Shi Q, Liu M, Sha J, Huang X, Wang PJ.

PLoS Genet. 2018 Jan 12;14(1):e1007175. doi: 10.1371/journal.pgen.1007175. eCollection 2018 Jan.


HORMAD1-dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes.

Kogo H, Tsutsumi M, Ohye T, Inagaki H, Abe T, Kurahashi H.

Genes Cells. 2012 Jun;17(6):439-54. doi: 10.1111/j.1365-2443.2012.01600.x. Epub 2012 Apr 25.


Meiotic homologue alignment and its quality surveillance are controlled by mouse HORMAD1.

Daniel K, Lange J, Hached K, Fu J, Anastassiadis K, Roig I, Cooke HJ, Stewart AF, Wassmann K, Jasin M, Keeney S, Tóth A.

Nat Cell Biol. 2011 May;13(5):599-610. doi: 10.1038/ncb2213. Epub 2011 Apr 10.


A G-quadruplex DNA structure resolvase, RHAU, is essential for spermatogonia differentiation.

Gao X, Ma W, Nie J, Zhang C, Zhang J, Yao G, Han J, Xu J, Hu B, Du Y, Shi Q, Yang Z, Huang X, Zhang Y.

Cell Death Dis. 2015 Jan 22;6:e1610. doi: 10.1038/cddis.2014.571.


Oogenesis requires germ cell-specific transcriptional regulators Sohlh1 and Lhx8.

Pangas SA, Choi Y, Ballow DJ, Zhao Y, Westphal H, Matzuk MM, Rajkovic A.

Proc Natl Acad Sci U S A. 2006 May 23;103(21):8090-5. Epub 2006 May 11.


Polo-like kinase is required for synaptonemal complex disassembly and phosphorylation in mouse spermatocytes.

Jordan PW, Karppinen J, Handel MA.

J Cell Sci. 2012 Nov 1;125(Pt 21):5061-72. doi: 10.1242/jcs.105015. Epub 2012 Aug 1.

Supplemental Content

Support Center