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Items: 1 to 50 of 106

1.

Genomic Structure of Hstx2 Modifier of Prdm9-Dependent Hybrid Male Sterility in Mice.

Lustyk D, Kinský S, Ullrich KK, Yancoskie M, Kašíková L, Gergelits V, Sedlacek R, Chan YF, Odenthal-Hesse L, Forejt J, Jansa P.

Genetics. 2019 Nov;213(3):1047-1063. doi: 10.1534/genetics.119.302554. Epub 2019 Sep 27.

PMID:
31562180
2.

Mouse ANKRD31 Regulates Spatiotemporal Patterning of Meiotic Recombination Initiation and Ensures Recombination between X and Y Sex Chromosomes.

Papanikos F, Clément JAJ, Testa E, Ravindranathan R, Grey C, Dereli I, Bondarieva A, Valerio-Cabrera S, Stanzione M, Schleiffer A, Jansa P, Lustyk D, Fei JF, Adams IR, Forejt J, Barchi M, de Massy B, Toth A.

Mol Cell. 2019 Jun 6;74(5):1069-1085.e11. doi: 10.1016/j.molcel.2019.03.022. Epub 2019 Apr 15.

PMID:
31000436
3.

Cisplatin-induced DNA double-strand breaks promote meiotic chromosome synapsis in PRDM9-controlled mouse hybrid sterility.

Wang L, Valiskova B, Forejt J.

Elife. 2018 Dec 28;7. pii: e42511. doi: 10.7554/eLife.42511.

4.

Modulation of Prdm9-controlled meiotic chromosome asynapsis overrides hybrid sterility in mice.

Gregorova S, Gergelits V, Chvatalova I, Bhattacharyya T, Valiskova B, Fotopulosova V, Jansa P, Wiatrowska D, Forejt J.

Elife. 2018 Mar 14;7. pii: e34282. doi: 10.7554/eLife.34282.

5.

High-Resolution Maps of Mouse Reference Populations.

Simecek P, Forejt J, Williams RW, Shiroishi T, Takada T, Lu L, Johnson TE, Bennett B, Deschepper CF, Scott-Boyer MP, Pardo-Manuel de Villena F, Churchill GA.

G3 (Bethesda). 2017 Oct 5;7(10):3427-3434. doi: 10.1534/g3.117.300188.

6.

Hybrid Sterility Locus on Chromosome X Controls Meiotic Recombination Rate in Mouse.

Balcova M, Faltusova B, Gergelits V, Bhattacharyya T, Mihola O, Trachtulec Z, Knopf C, Fotopulosova V, Chvatalova I, Gregorova S, Forejt J.

PLoS Genet. 2016 Apr 22;12(4):e1005906. doi: 10.1371/journal.pgen.1005906. eCollection 2016 Apr.

7.

Genetics: Asymmetric breaks in DNA cause sterility.

Forejt J.

Nature. 2016 Feb 11;530(7589):167-8. doi: 10.1038/nature16870. Epub 2016 Feb 3. No abstract available.

PMID:
26840487
8.

Maternal-foetal genomic conflict and speciation: no evidence for hybrid placental dysplasia in crosses between two house mouse subspecies.

Kropáčková L, Piálek J, Gergelits V, Forejt J, Reifová R.

J Evol Biol. 2015 Mar;28(3):688-98. doi: 10.1111/jeb.12602. Epub 2015 Mar 6.

9.

Dosage compensation of an aneuploid genome in mouse spermatogenic cells.

Jansa P, Homolka D, Blatny R, Mistrik M, Bartek J, Forejt J.

Biol Reprod. 2014 Jun;90(6):124. doi: 10.1095/biolreprod.114.118497. Epub 2014 Apr 30.

PMID:
24790161
10.

Prdm9 incompatibility controls oligospermia and delayed fertility but no selfish transmission in mouse intersubspecific hybrids.

Flachs P, Bhattacharyya T, Mihola O, Piálek J, Forejt J, Trachtulec Z.

PLoS One. 2014 Apr 22;9(4):e95806. doi: 10.1371/journal.pone.0095806. eCollection 2014.

11.

X chromosome control of meiotic chromosome synapsis in mouse inter-subspecific hybrids.

Bhattacharyya T, Reifova R, Gregorova S, Simecek P, Gergelits V, Mistrik M, Martincova I, Pialek J, Forejt J.

PLoS Genet. 2014 Feb 6;10(2):e1004088. doi: 10.1371/journal.pgen.1004088. eCollection 2014 Feb.

12.

Mechanistic basis of infertility of mouse intersubspecific hybrids.

Bhattacharyya T, Gregorova S, Mihola O, Anger M, Sebestova J, Denny P, Simecek P, Forejt J.

Proc Natl Acad Sci U S A. 2013 Feb 5;110(6):E468-77. doi: 10.1073/pnas.1219126110. Epub 2013 Jan 17.

13.

Interallelic and intergenic incompatibilities of the Prdm9 (Hst1) gene in mouse hybrid sterility.

Flachs P, Mihola O, Simeček P, Gregorová S, Schimenti JC, Matsui Y, Baudat F, de Massy B, Piálek J, Forejt J, Trachtulec Z.

PLoS Genet. 2012;8(11):e1003044. doi: 10.1371/journal.pgen.1003044. Epub 2012 Nov 1.

14.

Dissecting the genetic architecture of F1 hybrid sterility in house mice.

Dzur-Gejdosova M, Simecek P, Gregorova S, Bhattacharyya T, Forejt J.

Evolution. 2012 Nov;66(11):3321-35. doi: 10.1111/j.1558-5646.2012.01684.x. Epub 2012 May 25.

PMID:
23106700
15.

Chromosome substitution strains: gene discovery, functional analysis, and systems studies.

Nadeau JH, Forejt J, Takada T, Shiroishi T.

Mamm Genome. 2012 Oct;23(9-10):693-705. doi: 10.1007/s00335-012-9426-y. Epub 2012 Sep 8. Review.

16.
17.

Genetically enhanced asynapsis of autosomal chromatin promotes transcriptional dysregulation and meiotic failure.

Homolka D, Jansa P, Forejt J.

Chromosoma. 2012 Feb;121(1):91-104. doi: 10.1007/s00412-011-0346-5. Epub 2011 Oct 16.

18.

Differential expression of non-coding RNAs and continuous evolution of the X chromosome in testicular transcriptome of two mouse species.

Homolka D, Ivanek R, Forejt J, Jansa P.

PLoS One. 2011 Feb 14;6(2):e17198. doi: 10.1371/journal.pone.0017198.

19.

A mouse speciation gene encodes a meiotic histone H3 methyltransferase.

Mihola O, Trachtulec Z, Vlcek C, Schimenti JC, Forejt J.

Science. 2009 Jan 16;323(5912):373-5. doi: 10.1126/science.1163601. Epub 2008 Dec 11.

20.

PPARG by dietary fat interaction influences bone mass in mice and humans.

Ackert-Bicknell CL, Demissie S, Marín de Evsikova C, Hsu YH, DeMambro VE, Karasik D, Cupples LA, Ordovas JM, Tucker KL, Cho K, Canalis E, Paigen B, Churchill GA, Forejt J, Beamer WG, Ferrari S, Bouxsein ML, Kiel DP, Rosen CJ.

J Bone Miner Res. 2008 Sep;23(9):1398-408. doi: 10.1359/jbmr.080419.

21.

Segmental trisomy of mouse chromosome 17: introducing an alternative model of Down's syndrome.

Forejt J, Vacík T, Gregorová S.

Comp Funct Genomics. 2003;4(6):647-52. doi: 10.1002/cfg.334.

22.

Radio-opaque appearance of lanthanum carbonate in a patient with chronic renal failure.

Pafcugová J, Horácková M, Hrasková M, Forejt J, Szabo M, Pádr R.

Nephrol Dial Transplant. 2008 May;23(5):1776-7; author reply 1777-8. doi: 10.1093/ndt/gfn015. Epub 2008 Feb 18. No abstract available.

PMID:
18283090
23.

Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies.

Gregorová S, Divina P, Storchova R, Trachtulec Z, Fotopulosova V, Svenson KL, Donahue LR, Paigen B, Forejt J.

Genome Res. 2008 Mar;18(3):509-15. doi: 10.1101/gr.7160508. Epub 2008 Feb 6.

24.

Fine haplotype structure of a chromosome 17 region in the laboratory and wild mouse.

Trachtulec Z, Vlcek C, Mihola O, Gregorova S, Fotopulosova V, Forejt J.

Genetics. 2008 Mar;178(3):1777-84. doi: 10.1534/genetics.107.082404. Epub 2008 Feb 3.

25.

Identification of mutated Srebf1 as a QTL influencing risk for hepatic steatosis in the spontaneously hypertensive rat.

Pravenec M, Kazdova L, Landa V, Zidek V, Mlejnek P, Simakova M, Jansa P, Forejt J, Kren V, Krenova D, Qi N, Wang JM, Chan D, Aitman TJ, Kurtz TW.

Hypertension. 2008 Jan;51(1):148-53. Epub 2007 Dec 10.

PMID:
18071061
26.

Development of unique house mouse resources suitable for evolutionary studies of speciation.

Piálek J, Vyskocilová M, Bímová B, Havelková D, Piálková J, Dufková P, Bencová V, Dureje L, Albrecht T, Hauffe HC, Macholán M, Munclinger P, Storchová R, Zajícová A, Holán V, Gregorová S, Forejt J.

J Hered. 2008 Jan-Feb;99(1):34-44. Epub 2007 Oct 26.

PMID:
17965200
27.

Chromosomal rearrangement interferes with meiotic X chromosome inactivation.

Homolka D, Ivanek R, Capkova J, Jansa P, Forejt J.

Genome Res. 2007 Oct;17(10):1431-7. Epub 2007 Aug 23.

28.

Conserved alternative and antisense transcripts at the programmed cell death 2 locus.

Mihola O, Forejt J, Trachtulec Z.

BMC Genomics. 2007 Jan 18;8:20.

30.

Segmental trisomy of chromosome 17: a mouse model of human aneuploidy syndromes.

Vacík T, Ort M, Gregorová S, Strnad P, Blatny R, Conte N, Bradley A, Bures J, Forejt J.

Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4500-5. Epub 2005 Mar 8.

31.

Life-threatening renal failure caused by vasomotor nephropathy associated with nonsteroidal anti-inflammatory drugs.

Horackova M, Charvat J, Hasa J, Forejt J, Kvapil M.

Int J Clin Pharmacol Res. 2004;24(4):117-22.

PMID:
15754916
32.

Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order.

Divina P, Vlcek C, Strnad P, Paces V, Forejt J.

BMC Genomics. 2005 Mar 5;6:29.

33.

Behavioral characterization of wild derived male mice (Mus musculus musculus) of the PWD/Ph inbred strain: high exploration compared to C57BL/6J.

Fernandes C, Liu L, Paya-Cano JL, Gregorová S, Forejt J, Schalkwyk LC.

Behav Genet. 2004 Nov;34(6):621-30.

PMID:
15520518
34.

The Collaborative Cross, a community resource for the genetic analysis of complex traits.

Churchill GA, Airey DC, Allayee H, Angel JM, Attie AD, Beatty J, Beavis WD, Belknap JK, Bennett B, Berrettini W, Bleich A, Bogue M, Broman KW, Buck KJ, Buckler E, Burmeister M, Chesler EJ, Cheverud JM, Clapcote S, Cook MN, Cox RD, Crabbe JC, Crusio WE, Darvasi A, Deschepper CF, Doerge RW, Farber CR, Forejt J, Gaile D, Garlow SJ, Geiger H, Gershenfeld H, Gordon T, Gu J, Gu W, de Haan G, Hayes NL, Heller C, Himmelbauer H, Hitzemann R, Hunter K, Hsu HC, Iraqi FA, Ivandic B, Jacob HJ, Jansen RC, Jepsen KJ, Johnson DK, Johnson TE, Kempermann G, Kendziorski C, Kotb M, Kooy RF, Llamas B, Lammert F, Lassalle JM, Lowenstein PR, Lu L, Lusis A, Manly KF, Marcucio R, Matthews D, Medrano JF, Miller DR, Mittleman G, Mock BA, Mogil JS, Montagutelli X, Morahan G, Morris DG, Mott R, Nadeau JH, Nagase H, Nowakowski RS, O'Hara BF, Osadchuk AV, Page GP, Paigen B, Paigen K, Palmer AA, Pan HJ, Peltonen-Palotie L, Peirce J, Pomp D, Pravenec M, Prows DR, Qi Z, Reeves RH, Roder J, Rosen GD, Schadt EE, Schalkwyk LC, Seltzer Z, Shimomura K, Shou S, Sillanpää MJ, Siracusa LD, Snoeck HW, Spearow JL, Svenson K, Tarantino LM, Threadgill D, Toth LA, Valdar W, de Villena FP, Warden C, Whatley S, Williams RW, Wiltshire T, Yi N, Zhang D, Zhang M, Zou F; Complex Trait Consortium.

Nat Genet. 2004 Nov;36(11):1133-7.

PMID:
15514660
35.

Genetic analysis of X-linked hybrid sterility in the house mouse.

Storchová R, Gregorová S, Buckiová D, Kyselová V, Divina P, Forejt J.

Mamm Genome. 2004 Jul;15(7):515-24.

PMID:
15366371
36.

The European dimension for the mouse genome mutagenesis program.

Auwerx J, Avner P, Baldock R, Ballabio A, Balling R, Barbacid M, Berns A, Bradley A, Brown S, Carmeliet P, Chambon P, Cox R, Davidson D, Davies K, Duboule D, Forejt J, Granucci F, Hastie N, de Angelis MH, Jackson I, Kioussis D, Kollias G, Lathrop M, Lendahl U, Malumbres M, von Melchner H, Müller W, Partanen J, Ricciardi-Castagnoli P, Rigby P, Rosen B, Rosenthal N, Skarnes B, Stewart AF, Thornton J, Tocchini-Valentini G, Wagner E, Wahli W, Wurst W.

Nat Genet. 2004 Sep;36(9):925-7. Erratum in: Nat Genet. 2004 Nov;36(11):1238.

37.

Comparative analysis of the PDCD2-TBP-PSMB1 region in vertebrates.

Trachtulec Z, Vlcek C, Mihola O, Forejt J.

Gene. 2004 Jun 23;335:151-7.

PMID:
15194198
38.

The Mouse SAGE Site: database of public mouse SAGE libraries.

Divina P, Forejt J.

Nucleic Acids Res. 2004 Jan 1;32(Database issue):D482-3.

39.
40.

Accumulation of the proteolytic marker peptide ubiquitin in the trophoblast of mammalian blastocysts.

Sutovsky P, Motlik J, Neuber E, Pavlok A, Schatten G, Palecek J, Hyttel P, Adebayo OT, Adwan K, Alberio R, Bagis H, Bataineh Z, Bjerregaard B, Bodo S, Bryja V, Carrington M, Couf M, de la Fuente R, Diblik J, Esner M, Forejt J, Fulka J Jr, Geussova G, Gjorret JO, Libik M, Hampl A, Hassane MS, Houshmand M, Hozak P, Jezova M, Kania G, Kanka J, Kandil OM, Kishimoto T, Klima J, Kohoutek J, Kopska T, Kubelka M, Lapathitis G, Laurincik J, Lefevre B, Mihalik J, Novakova M, Oko R, Omelka R, Owiny D, Pachernik J, Pacholikova J, Peknicova J, Pesty A, Ponya Z, Preclikova H, Sloskova A, Svoboda P, Strejcek F, Toth S, Tepla O, Valdivia M, Vodicka P, Zudova D.

Cloning Stem Cells. 2001;3(3):157-61.

PMID:
11945225
41.

[Pharmacologic insult as a cause of acute kidney failure with a need for acute hemodialysis therapy].

Forejt J, Horácková M, Hása J, Safárová R, Vanková S, Votocek J.

Vnitr Lek. 2001 Nov;47(11):733-8. Czech.

PMID:
11795176
42.

Expression of BRCA1, NBR1 and NBR2 genes in human breast cancer cells.

Dimitrov SD, Matousková E, Forejt J.

Folia Biol (Praha). 2001;47(4):120-7.

PMID:
11508855
43.

[Central salt-wasting diuresis syndrome as a cause of hyponatremia in patients at the internal medicine department].

Safárová R, Horácková M, Vanková S, Forejt J, Hása J.

Vnitr Lek. 2001 Jul;47(7):484-7. Czech.

PMID:
11505721
44.

Identification of a mutation in ADD1/SREBP-1 in the spontaneously hypertensive rat.

Pravenec M, Jansa P, Kostka V, Zídek V, Kren V, Forejt J, Kurtz TW.

Mamm Genome. 2001 Apr;12(4):295-8.

PMID:
11309661
45.

The nomenclature of major histocompatibility complex class I gene regulatory regions -- the case of two different downstream regulatory elements.

Hatina J, Jansa P, Forejt J.

Mol Immunol. 2000 Aug-Sep;37(12-13):799-800. No abstract available.

PMID:
11286219
46.

Synteny of orthologous genes conserved in mammals, snake, fly, nematode, and fission yeast.

Trachtulec Z, Forejt J.

Mamm Genome. 2001 Mar;12(3):227-31.

PMID:
11252172
47.

Expression profiles and intergenic structure of head-to-head oriented Brca1 and Nbr1 genes.

Dimitrov S, Brennerova M, Forejt J.

Gene. 2001 Jan 10;262(1-2):89-98.

PMID:
11179671
48.
49.

New resources of functional genomics: unique vertebrate models from Prague.

Forejt J.

Folia Biol (Praha). 2000;46(1):1-2. No abstract available.

PMID:
10730875
50.

Monoallelic expression of reactivated imprinted genes in embryonal carcinoma cell hybrids.

Forejt J, Saam JR, Gregorová S, Tilghman SM.

Exp Cell Res. 1999 Nov 1;252(2):416-22.

PMID:
10527631

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