-
1
-
-
0035319804
-
To err (meiotically) is human: The genesis of human aneuploidy
-
doi:10.1038/35066065. PubMed: 11283700
-
Hassold T, Hunt P (2001) To err (meiotically) is human: the genesis of human aneuploidy. Nat Rev Genet 2: 280-291. doi:10.1038/35066065. PubMed: 11283700.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 280-291
-
-
Hassold, T.1
Hunt, P.2
-
2
-
-
0000049938
-
Chromosome Abnormalities in Human Reproductive Wastage
-
doi: 10.1016/0168-9525(86)90194-0
-
Hassold T (1986) Chromosome Abnormalities in Human Reproductive Wastage. Trends Genet 2: 105-110. doi: 10.1016/0168-9525(86)90194-0.
-
(1986)
Trends Genet
, vol.2
, pp. 105-110
-
-
Hassold, T.1
-
3
-
-
0029818072
-
Human aneuploidy: Incidence, origin, and etiology
-
Available online at: doi:10.1002/(SICI)1098-2280(1996)28:3<167:AID-E
-
Hassold T, Abruzzo M, Adkins K, Griffin D, Merrill M et al. (1996) Human aneuploidy: Incidence, origin, and etiology. Environ Mol Mutagen 28: 167-175. Available online at: doi:10.1002/(SICI)1098-2280(1996)28:3<167:AID-EM2>3. 0.CO;2-B.
-
(1996)
Environ Mol Mutagen
, vol.28
, pp. 167-175
-
-
Hassold, T.1
Abruzzo, M.2
Adkins, K.3
Griffin, D.4
Merrill, M.5
-
4
-
-
84863892710
-
Human aneuploidy: Mechanisms and new insights into an age-old problem
-
doi:10.1038/nrg3245. PubMed: 22705668
-
Nagaoka SI, Hassold TJ, Hunt PA (2012) Human aneuploidy: mechanisms and new insights into an age-old problem. Nat Rev Genet 13: 493-504. doi:10.1038/nrg3245. PubMed: 22705668.
-
(2012)
Nat Rev Genet
, vol.13
, pp. 493-504
-
-
Nagaoka, S.I.1
Hassold, T.J.2
Hunt, P.A.3
-
5
-
-
0030003995
-
Exchanges are not equally able to enhance meiotic chromosome segregation in yeast
-
doi:10.1073/pnas.93.10.4979. PubMed: 8643515
-
Ross LO, Maxfield R, Dawson D (1996) Exchanges are not equally able to enhance meiotic chromosome segregation in yeast. Proc Natl Acad Sci U S A 93: 4979-4983. doi:10.1073/pnas.93.10.4979. PubMed: 8643515.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 4979-4983
-
-
Ross, L.O.1
Maxfield, R.2
Dawson, D.3
-
6
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
doi:10.1038/ng0796-336. PubMed: 8673133
-
Baker SM, Plug AW, Prolla TA, Bronner CE, Harris AC et al. (1996) Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat Genet 13: 336-342. doi:10.1038/ng0796-336. PubMed: 8673133.
-
(1996)
Nat Genet
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
Bronner, C.E.4
Harris, A.C.5
-
7
-
-
0029118422
-
Recombination and maternal age-dependent nondisjunction: Molecular studies of trisomy 16
-
PubMed: 7573048
-
Hassold T, Merrill M, Adkins K, Freeman S, Sherman S (1995) Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. Am J Hum Genet 57: 867-874. PubMed: 7573048.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 867-874
-
-
Hassold, T.1
Merrill, M.2
Adkins, K.3
Freeman, S.4
Sherman, S.5
-
8
-
-
0034001512
-
Down syndrome: Genetic recombination and the origin of the extra chromosome 21
-
doi: 10.1034/j.1399-0004.2000.570201.x. PubMed: 10735628
-
Hassold T, Sherman S (2000) Down syndrome: genetic recombination and the origin of the extra chromosome 21. Clin Genet 57: 95-100. doi: 10.1034/j.1399-0004.2000.570201.x. PubMed: 10735628.
-
(2000)
Clin Genet
, vol.57
, pp. 95-100
-
-
Hassold, T.1
Sherman, S.2
-
9
-
-
0023236677
-
Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome
-
doi: 10.1126/science.2955519. PubMed: 2955519
-
Warren AC, Chakravarti A, Wong C, Slaugenhaupt SA, Halloran SL et al. (1987) Evidence for Reduced Recombination on the Nondisjoined Chromosomes 21 in Down Syndrome. Science 237: 652-654. doi: 10.1126/science.2955519. PubMed: 2955519.
-
(1987)
Science
, vol.237
, pp. 652-654
-
-
Warren, A.C.1
Chakravarti, A.2
Wong, C.3
Slaugenhaupt, S.A.4
Halloran, S.L.5
-
10
-
-
5444246038
-
Variation in Human Meiotic Recombination
-
doi: 10.1146/annurev.genom.4.070802.110217. PubMed: 15485352
-
Lynn A, Ashley T, Hassold T (2004) Variation in Human Meiotic Recombination. Annu Rev Genomics Hum Genet 5: 317-349. doi: 10.1146/annurev. genom.4.070802.110217. PubMed: 15485352.
-
(2004)
Annu Rev Genomics Hum Genet
, vol.5
, pp. 317-349
-
-
Lynn, A.1
Ashley, T.2
Hassold, T.3
-
11
-
-
0032231877
-
Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination
-
doi: 10.1086/302011. PubMed: 9718341
-
Broman KW, Murray JC, Sheffield VC, White RL, Weber JL (1998) Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination. Am J Hum Genet 63: 861-869. doi: 10.1086/302011. PubMed: 9718341.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
12
-
-
19944431111
-
Ethnicity and Human Genetic Linkage Maps
-
doi:10.1086/427926. PubMed: 15627237
-
Jorgenson E, Tang H, Gadde M, Province M, Leppert M et al. (2005) Ethnicity and Human Genetic Linkage Maps. Am J Hum Genet 76: 276-290. doi:10.1086/427926. PubMed: 15627237.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 276-290
-
-
Jorgenson, E.1
Tang, H.2
Gadde, M.3
Province, M.4
Leppert, M.5
-
13
-
-
58149331851
-
A genome-wide Asian genetic map and ethnic comparison: The GENDISCAN study
-
doi:10.1186/1471-2164-9-554. PubMed: 19025666
-
Ju YS, Park H, Lee MK, Kim J-I, Sung J et al. (2008) A genome-wide Asian genetic map and ethnic comparison: The GENDISCAN study. BMC Genomics 9: 554. doi:10.1186/1471-2164-9-554. PubMed: 19025666.
-
(2008)
BMC Genomics
, vol.9
, pp. 554
-
-
Ju, Y.S.1
Park, H.2
Lee, M.K.3
Kim, J.-I.4
Sung, J.5
-
14
-
-
38849084666
-
A second-generation combined linkage-physical map of the human genome
-
doi:10.1101/gr.7156307. PubMed: 17989245
-
Matise TC, Chen F, Chen W, Vega FMDL, Hansen M et al. (2007) A second-generation combined linkage-physical map of the human genome. Genome Res 17: 1783-1786. doi:10.1101/gr.7156307. PubMed: 17989245.
-
(2007)
Genome Res
, vol.17
, pp. 1783-1786
-
-
Matise, T.C.1
Chen, F.2
Chen, W.3
Fmdl, V.4
Hansen, M.5
-
15
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
doi:10.1038/ng917. PubMed: 12053178
-
Kong A, Gudbjartsson DF, Sainz J, Jonsdottir GM, Gudjonsson SA et al. (2002) A high-resolution recombination map of the human genome. Nat Genet 31: 241-247. doi:10.1038/ng917. PubMed: 12053178.
-
(2002)
Nat Genet
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
-
16
-
-
0032918559
-
Distribution of Crossing Over on Mouse Synaptonemal Complexes Using Immunofluorescent Localization of MLH1 Protein
-
PubMed: 10101178
-
Anderson LK, Reeves A, Webb LM, Ashley T (1999) Distribution of Crossing Over on Mouse Synaptonemal Complexes Using Immunofluorescent Localization of MLH1 Protein. Genetics 151: 1569-1579. PubMed: 10101178.
-
(1999)
Genetics
, vol.151
, pp. 1569-1579
-
-
Anderson, L.K.1
Reeves, A.2
Webb, L.M.3
Ashley, T.4
-
17
-
-
52949098362
-
MUS81 Generates a Subset of MLH1-MLH3-Independent Crossovers in Mammalian Meiosis
-
doi:10.1371/journal.pgen.1000186
-
Holloway JK, Booth J, Edelmann W, McGowan CH, Cohen PE (2008) MUS81 Generates a Subset of MLH1-MLH3-Independent Crossovers in Mammalian Meiosis. PLOS Genet 4: e1000186. doi:10.1371/journal.pgen.1000186.
-
(2008)
PLOS Genet
, vol.4
-
-
Holloway, J.K.1
Booth, J.2
Edelmann, W.3
McGowan, C.H.4
Cohen, P.E.5
-
18
-
-
0037854709
-
The Mus81/Mms4 Endonuclease Acts Independently of Double-Holliday Junction Resolution to Promote a Distinct Subset of Crossovers During Meiosis in Budding Yeast
-
PubMed: 12750322
-
de los Santos T, Hunter N, Lee C, Larkin B, Loidl J et al. (2003) The Mus81/Mms4 Endonuclease Acts Independently of Double-Holliday Junction Resolution to Promote a Distinct Subset of Crossovers During Meiosis in Budding Yeast. Genetics 164: 81-94. PubMed: 12750322.
-
(2003)
Genetics
, vol.164
, pp. 81-94
-
-
De Los Santos, T.1
Hunter, N.2
Lee, C.3
Larkin, B.4
Loidl, J.5
-
19
-
-
5644225562
-
Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells
-
doi:10.1159/000080599. PubMed: 15467366
-
Tease C, Hultén MA (2004) Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells. Cytogenet Genome Res 107: 208-215. doi:10.1159/000080599. PubMed: 15467366.
-
(2004)
Cytogenet Genome Res
, vol.107
, pp. 208-215
-
-
Tease, C.1
Hultén, M.A.2
-
20
-
-
0031829611
-
Crossing over analysis at pachytene in man
-
doi:10.1038/sj.ejhg.5200200. PubMed: 9781043
-
Barlow AL, Hultén Ma (1998) Crossing over analysis at pachytene in man. Eur J Hum Genet 6: 350-358. doi:10.1038/sj.ejhg.5200200. PubMed: 9781043.
-
(1998)
Eur J Hum Genet
, vol.6
, pp. 350-358
-
-
Barlow, A.L.1
Hultén, M.A.2
-
21
-
-
70349659695
-
Meiotic recombination in human oocytes
-
doi:10.1371/journal.pgen.1000661. PubMed: 19763179
-
Cheng EY, Hunt PA, Naluai-Cecchini TA, Fligner CL, Fujimoto VY et al. (2009) Meiotic recombination in human oocytes. PLoS Genet 5: e1000661. doi:10.1371/journal.pgen.1000661. PubMed: 19763179.
-
(2009)
PLoS Genet
, vol.5
-
-
Cheng, E.Y.1
Hunt, P.A.2
Naluai-Cecchini, T.A.3
Fligner, C.L.4
Fujimoto, V.Y.5
-
22
-
-
11144325648
-
Extreme Heterogeneity in the Molecular Events Leading to the Establishment of Chiasmata during Meiosis I in Human Oocytes
-
doi:10.1086/427268. PubMed: 15558497
-
Lenzi ML, Smith J, Snowden T, Kim M, Fishel R et al. (2005) Extreme Heterogeneity in the Molecular Events Leading to the Establishment of Chiasmata during Meiosis I in Human Oocytes. Am J Hum Genet 76: 112-127. doi:10.1086/427268. PubMed: 15558497.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 112-127
-
-
Lenzi, M.L.1
Smith, J.2
Snowden, T.3
Kim, M.4
Fishel, R.5
-
23
-
-
5644293069
-
Cytological studies of meiotic recombination in human males
-
doi:10.1159/000080602. PubMed: 15467369
-
Hassold T, Judis L, Chan ER, Schwartz S, Seftel A et al. (2004) Cytological studies of meiotic recombination in human males. Cytogenet Genome Res 107: 249-255. doi:10.1159/000080602. PubMed: 15467369.
-
(2004)
Cytogenet Genome Res
, vol.107
, pp. 249-255
-
-
Hassold, T.1
Judis, L.2
Chan, E.R.3
Schwartz, S.4
Seftel, A.5
-
24
-
-
9444239304
-
Defective recombination in infertile men
-
doi:10.1093/hmg/ddh302. PubMed: 15385442
-
Gonsalves J, Sun F, Schlegel PN, Turek PJ, Hopps CV et al. (2004) Defective recombination in infertile men. Hum Mol Genet 13: 2875-2883. doi:10.1093/hmg/ddh302. PubMed: 15385442.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2875-2883
-
-
Gonsalves, J.1
Sun, F.2
Schlegel, P.N.3
Turek, P.J.4
Hopps, C.V.5
-
25
-
-
45549099981
-
The relationship between meiotic recombination in human spermatocytes and aneuploidy in sperm
-
doi:10.1093/humrep/den027. PubMed: 18482994
-
Sun F, Mikhaail-Philips M, Oliver-Bonet M, Ko E, Rademaker A et al. (2008) The relationship between meiotic recombination in human spermatocytes and aneuploidy in sperm. Hum Reprod 23: 1691-1697. doi:10.1093/humrep/den027. PubMed: 18482994.
-
(2008)
Hum Reprod
, vol.23
, pp. 1691-1697
-
-
Sun, F.1
Mikhaail-Philips, M.2
Oliver-Bonet, M.3
Ko, E.4
Rademaker, A.5
-
26
-
-
33645514471
-
Crossover frequency and synaptonemal complex length: Their variability and effects on human male meiosis
-
doi:10.1093/molehr/gal007. PubMed: 16449239
-
Codina-Pascual M, Campillo M, Kraus J, Speicher MR, Egozcue J et al. (2006) Crossover frequency and synaptonemal complex length: their variability and effects on human male meiosis. Mol Hum Reprod 12: 123-133. doi:10.1093/molehr/gal007. PubMed: 16449239.
-
(2006)
Mol Hum Reprod
, vol.12
, pp. 123-133
-
-
Codina-Pascual, M.1
Campillo, M.2
Kraus, J.3
Speicher, M.R.4
Egozcue, J.5
-
27
-
-
33747891214
-
Variation in MLH1 distribution in recombination maps for individual chromosomes from human males
-
doi: 10.1093/hmg/ddl162. PubMed: 16803849
-
Sun F, Oliver-Bonet M, Liehr T, Starke H, Turek P et al. (2006) Variation in MLH1 distribution in recombination maps for individual chromosomes from human males. Hum Mol Genet 15: 2376-2391. doi: 10.1093/hmg/ddl162. PubMed: 16803849.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2376-2391
-
-
Sun, F.1
Oliver-Bonet, M.2
Liehr, T.3
Starke, H.4
Turek, P.5
-
28
-
-
0037150706
-
Covariation of Synaptonemal Complex Length and Mammalian Meiotic Exchange Rates
-
doi:10.1126/science.1071220. PubMed: 12052900
-
Lynn A, Koehler KE, Judis L, Chan ER, Cherry JP et al. (2002) Covariation of Synaptonemal Complex Length and Mammalian Meiotic Exchange Rates. Science 296: 2222-2225. doi:10.1126/science.1071220. PubMed: 12052900.
-
(2002)
Science
, vol.296
, pp. 2222-2225
-
-
Lynn, A.1
Koehler, K.E.2
Judis, L.3
Chan, E.R.4
Cherry, J.P.5
-
29
-
-
25444478350
-
Meiotic Synapsis Proceeds from a Limited Number of Subtelomeric Sites in the Human Male
-
doi: 10.1086/468188. PubMed: 16175502
-
Brown PW, Judis L, Chan ER, Schwartz S, Seftel A et al. (2005) Meiotic Synapsis Proceeds from a Limited Number of Subtelomeric Sites in the Human Male. Am J Hum Genet 77: 556-566. doi: 10.1086/468188. PubMed: 16175502.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 556-566
-
-
Brown, P.W.1
Judis, L.2
Chan, E.R.3
Schwartz, S.4
Seftel, A.5
-
30
-
-
0021700771
-
The Synaptonemal Complex in Genetic Segregation
-
doi: 10.1146/annurev.ge.18.120184.001555. PubMed: 6241453
-
Wettstein D, Rasmussen SW, Holm PB (1984) The Synaptonemal Complex in Genetic Segregation. Annu Rev Genet 18: 331-411. doi: 10.1146/annurev.ge.18. 120184.001555. PubMed: 6241453.
-
(1984)
Annu Rev Genet
, vol.18
, pp. 331-411
-
-
Wettstein, D.1
Rasmussen, S.W.2
Holm, P.B.3
-
31
-
-
34547673378
-
Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis
-
doi:10.1007/s10577-007-1140-3. PubMed: 17674146
-
Baudat F, de Massy B (2007) Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis. Chromosome Res 15: 565-577. doi:10.1007/s10577-007-1140-3. PubMed: 17674146.
-
(2007)
Chromosome Res
, vol.15
, pp. 565-577
-
-
Baudat, F.1
De Massy, B.2
-
32
-
-
0032127849
-
Role of the human RAD51 protein in homologous recombination and double-stranded-break repair
-
doi:10.1016/S0968-0004(98)01232-8. PubMed: 9697414
-
Baumann P, West SC (1998) Role of the human RAD51 protein in homologous recombination and double-stranded-break repair. Trends Biochem Sci 23: 247-251. doi:10.1016/S0968-0004(98)01232-8. PubMed: 9697414.
-
(1998)
Trends Biochem Sci
, vol.23
, pp. 247-251
-
-
Baumann, P.1
West, S.C.2
-
33
-
-
0030818573
-
Distribution of the Rad51 recombinase in human and mouse spermatocytes
-
doi:10.1093/emboj/16.17.5207. PubMed: 9311981
-
Barlow AL, Benson FE, West SC, Hultén MA (1997) Distribution of the Rad51 recombinase in human and mouse spermatocytes. EMBO J 16: 5207-5215. doi:10.1093/emboj/16.17.5207. PubMed: 9311981.
-
(1997)
EMBO J
, vol.16
, pp. 5207-5215
-
-
Barlow, A.L.1
Benson, F.E.2
West, S.C.3
Hultén, M.A.4
-
34
-
-
24344445963
-
Temporal progression of recombination in human males
-
doi:10.1093/molehr/gah193. PubMed: 16123081
-
Oliver-Bonet M, Turek PJ, Sun F, Ko E, Martin RH (2005) Temporal progression of recombination in human males. Mol Hum Reprod 11: 517-522. doi:10.1093/molehr/gah193. PubMed: 16123081.
-
(2005)
Mol Hum Reprod
, vol.11
, pp. 517-522
-
-
Oliver-Bonet, M.1
Turek, P.J.2
Sun, F.3
Ko, E.4
Martin, R.H.5
-
35
-
-
0034697965
-
Zip3 Provides a Link between Recombination Enzymes and Synaptonemal Complex Proteins
-
doi:10.1016/S0092-8674(00)00029-5. PubMed: 10943844
-
Agarwal S, Roeder GS (2000) Zip3 Provides a Link between Recombination Enzymes and Synaptonemal Complex Proteins. Cell 102: 245-255. doi:10.1016/S0092-8674(00)00029-5. PubMed: 10943844.
-
(2000)
Cell
, vol.102
, pp. 245-255
-
-
Agarwal, S.1
Roeder, G.S.2
-
36
-
-
0026697409
-
Correlation between pairing initiation sites, recombination nodules and meiotic recombination in Sordaria macrospora
-
PubMed: 1398050
-
Zickler D, Moreau PJ, Huynh AD, Slezec AM (1992) Correlation between pairing initiation sites, recombination nodules and meiotic recombination in Sordaria macrospora. Genetics 132: 135-148. PubMed: 1398050.
-
(1992)
Genetics
, vol.132
, pp. 135-148
-
-
Zickler, D.1
Moreau, P.J.2
Huynh, A.D.3
Slezec, A.M.4
-
37
-
-
34848815083
-
The origin of trisomy 13
-
doi:10.1002/ajmg.a.31913. PubMed: 17853475
-
Hall HE, Chan ER, Collins A, Judis L, Shirley S et al. (2007) The origin of trisomy 13. Am J Med Genet A 143A: 2242-2248. doi:10.1002/ajmg.a.31913. PubMed: 17853475.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 2242-2248
-
-
Hall, H.E.1
Chan, E.R.2
Collins, A.3
Judis, L.4
Shirley, S.5
-
38
-
-
65649140050
-
Cytological studies of recombination in rhesus males
-
doi:10.1159/000207519. PubMed: 19420925
-
Hassold T, Hansen T, Hunt P, VandeVoort C (2009) Cytological studies of recombination in rhesus males. Cytogenet Genome Res 124: 132-138. doi:10.1159/000207519. PubMed: 19420925.
-
(2009)
Cytogenet Genome Res
, vol.124
, pp. 132-138
-
-
Hassold, T.1
Hansen, T.2
Hunt, P.3
VandeVoort, C.4
-
39
-
-
84867919854
-
Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey
-
doi:10.1073/pnas.1207854109. PubMed: 23012422
-
Hunt PA, Lawson C, Gieske M, Murdoch B, Smith H et al. (2012) Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey. Proc Natl Acad Sci U S A 109: 17525-17530. doi:10.1073/pnas.1207854109. PubMed: 23012422.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 17525-17530
-
-
Hunt, P.A.1
Lawson, C.2
Gieske, M.3
Murdoch, B.4
Smith, H.5
-
40
-
-
67349172256
-
A New Standard Genetic Map for the Laboratory Mouse
-
doi:10.1534/genetics.109.105486. PubMed: 19535546
-
Cox A, Ackert-Bicknell CL, Dumont BL, Ding Y, Bell JT et al. (2009) A New Standard Genetic Map for the Laboratory Mouse. Genetics 182: 1335-1344. doi:10.1534/genetics.109.105486. PubMed: 19535546.
-
(2009)
Genetics
, vol.182
, pp. 1335-1344
-
-
Cox, A.1
Ackert-Bicknell, C.L.2
Dumont, B.L.3
Ding, Y.4
Bell, J.T.5
-
41
-
-
80755175828
-
A Pathway for Synapsis Initiation during Zygotene in Drosophila Oocytes
-
doi:10.1016/j.cub.2011.10.005. PubMed: 22036181
-
Tanneti NS, Landy K, Joyce EF, McKim KS (2011) A Pathway for Synapsis Initiation during Zygotene in Drosophila Oocytes. Curr Biol 21: 1852-1857. doi:10.1016/j.cub.2011.10.005. PubMed: 22036181.
-
(2011)
Curr Biol
, vol.21
, pp. 1852-1857
-
-
Tanneti, N.S.1
Landy, K.2
Joyce, E.F.3
McKim, K.S.4
-
42
-
-
84874617280
-
RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis
-
doi:10.1038/ng.2541. PubMed: 23396135
-
Reynolds A, Qiao H, Yang Y, Chen JK, Jackson N et al. (2013) RNF212 is a dosage-sensitive regulator of crossing-over during mammalian meiosis. Nat Genet 45: 269-278. doi:10.1038/ng.2541. PubMed: 23396135.
-
(2013)
Nat Genet
, vol.45
, pp. 269-278
-
-
Reynolds, A.1
Qiao, H.2
Yang, Y.3
Chen, J.K.4
Jackson, N.5
-
43
-
-
39449106471
-
Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate
-
doi: 10.1126/science.1152422. PubMed: 18239089
-
Kong A, Thorleifsson G, Stefansson H, Masson G, Helgason A et al. (2008) Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate. Science 319: 1398-1401. doi: 10.1126/science.1152422. PubMed: 18239089.
-
(2008)
Science
, vol.319
, pp. 1398-1401
-
-
Kong, A.1
Thorleifsson, G.2
Stefansson, H.3
Masson, G.4
Helgason, A.5
-
44
-
-
70349659703
-
Genetic Analysis of Variation in Human Meiotic Recombination
-
doi:10.1371/journal.pgen.1000648. PubMed: 19763160
-
Chowdhury R, Bois PRJ, Feingold E, Sherman SL, Cheung VG (2009) Genetic Analysis of Variation in Human Meiotic Recombination. PLoS Genet 5: e1000648. doi:10.1371/journal.pgen.1000648. PubMed: 19763160.
-
(2009)
PLoS Genet
, vol.5
-
-
Chowdhury, R.1
Bois, P.R.J.2
Feingold, E.3
Sherman, S.L.4
Cheung, V.G.5
-
45
-
-
79959257505
-
Variation in Human Recombination Rates and Its Genetic Determinants
-
doi:10.1371/journal.pone.0020321. PubMed: 21698098
-
Fledel-Alon A, Leffler EM, Guan Y, Stephens M, Coop G et al. (2011) Variation in Human Recombination Rates and Its Genetic Determinants. PLOS ONE 6: e20321. doi:10.1371/journal.pone.0020321. PubMed: 21698098.
-
(2011)
PLOS ONE
, vol.6
-
-
Fledel-Alon, A.1
Leffler, E.M.2
Guan, Y.3
Stephens, M.4
Coop, G.5
-
46
-
-
13944278863
-
A common inversion under selection in Europeans
-
doi:10.1038/ng1508. PubMed: 15654335
-
Stefansson H, Helgason A, Thorleifsson G, Steinthorsdottir V, Masson G et al. (2005) A common inversion under selection in Europeans. Nat Genet 37: 129-137. doi:10.1038/ng1508. PubMed: 15654335.
-
(2005)
Nat Genet
, vol.37
, pp. 129-137
-
-
Stefansson, H.1
Helgason, A.2
Thorleifsson, G.3
Steinthorsdottir, V.4
Masson, G.5
-
47
-
-
78149474587
-
Epigenetic Transitions in Germ Cell Development and Meiosis
-
doi:10.1016/j.devcel.2010.10.009. PubMed: 21074718
-
Kota SK, Feil R (2010) Epigenetic Transitions in Germ Cell Development and Meiosis. Dev Cell 19: 675-686. doi:10.1016/j.devcel.2010.10.009. PubMed: 21074718.
-
(2010)
Dev Cell
, vol.19
, pp. 675-686
-
-
Kota, S.K.1
Feil, R.2
-
48
-
-
84879249639
-
Conceptual links between DNA methylation reprogramming in the early embryo and primordial germ cells
-
doi:10.1016/j.ceb.2013.02.013. PubMed: 23510682
-
Seisenberger S, Peat JR, Reik W (2013) Conceptual links between DNA methylation reprogramming in the early embryo and primordial germ cells. Curr Opin Cell Biol 25: 281-288. doi:10.1016/j.ceb.2013.02.013. PubMed: 23510682.
-
(2013)
Curr Opin Cell Biol
, vol.25
, pp. 281-288
-
-
Seisenberger, S.1
Peat, J.R.2
Reik, W.3
-
49
-
-
0036768615
-
Epigenetic reprogramming in mouse primordial germ cells
-
doi:10.1016/S0925-4773(02)00181-8. PubMed: 12204247
-
Hajkova P, Erhardt S, Lane N, Haaf T, El-Maarri O et al. (2002) Epigenetic reprogramming in mouse primordial germ cells. Mech Dev 117: 15-23. doi:10.1016/S0925-4773(02)00181-8. PubMed: 12204247.
-
(2002)
Mech Dev
, vol.117
, pp. 15-23
-
-
Hajkova, P.1
Erhardt, S.2
Lane, N.3
Haaf, T.4
El-Maarri, O.5
-
50
-
-
77249148019
-
Genomewide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency
-
doi:10.1038/nature08829. PubMed: 20098412
-
Popp C, Dean W, Feng S, Cokus SJ, Andrews S et al. (2010) Genomewide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency. Nature 463: 1101-1105. doi:10.1038/nature08829. PubMed: 20098412.
-
(2010)
Nature
, vol.463
, pp. 1101-1105
-
-
Popp, C.1
Dean, W.2
Feng, S.3
Cokus, S.J.4
Andrews, S.5
-
51
-
-
7944221225
-
Timing of establishment of paternal methylation imprints in the mouse
-
doi:10.1016/j.ygeno.2004.08.012. PubMed: 15533712
-
Li J-Y, Lees-Murdock DJ, Xu G-L, Walsh CP (2004) Timing of establishment of paternal methylation imprints in the mouse. Genomics 84: 952-960. doi:10.1016/j.ygeno.2004.08.012. PubMed: 15533712.
-
(2004)
Genomics
, vol.84
, pp. 952-960
-
-
Li, J.-Y.1
Lees-Murdock, D.J.2
Xu, G.-L.3
Walsh, C.P.4
-
52
-
-
1842529388
-
Reproductive epigenetics
-
doi:10.1111/j.0009-9163.2004.00236.x. PubMed: 15025714
-
Kelly TL, Trasler JM (2004) Reproductive epigenetics. Clin Genet 65: 247-260. doi:10.1111/j.0009-9163.2004.00236.x. PubMed: 15025714.
-
(2004)
Clin Genet
, vol.65
, pp. 247-260
-
-
Kelly, T.L.1
Trasler, J.M.2
-
53
-
-
0032079514
-
Suppression of crossing-over by DNA methylation in Ascobolus
-
doi:10.1101/gad.12.9.1381. PubMed: 9573054
-
Maloisel L, Rossignol J-L (1998) Suppression of crossing-over by DNA methylation in Ascobolus. Genes Dev 12: 1381-1389. doi:10.1101/gad.12.9.1381. PubMed: 9573054.
-
(1998)
Genes Dev
, vol.12
, pp. 1381-1389
-
-
Maloisel, L.1
Rossignol, J.-L.2
-
54
-
-
84859620561
-
Deficiency in DNA methylation increases meiotic crossover rates in euchromatic but not in heterochromatic regions in Arabidopsis
-
doi:10.1073/pnas.1120742109. PubMed: 22460791
-
Melamed-Bessudo C, Levy AA (2012) Deficiency in DNA methylation increases meiotic crossover rates in euchromatic but not in heterochromatic regions in Arabidopsis. Proc Natl Acad Sci U S A 109: E981-E988. doi:10.1073/pnas. 1120742109. PubMed: 22460791.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
-
-
Melamed-Bessudo, C.1
Levy, A.A.2
-
55
-
-
84866168941
-
Epigenetic Remodeling of Meiotic Crossover Frequency in Arabidopsis thaliana DNA Methyltransferase Mutants
-
doi:10.1371/journal.pgen.1002844. PubMed: 22876192
-
Yelina NE, Choi K, Chelysheva L, Macaulay M, de Snoo B et al. (2012) Epigenetic Remodeling of Meiotic Crossover Frequency in Arabidopsis thaliana DNA Methyltransferase Mutants. PLoS Genet 8: e1002844. doi:10.1371/journal.pgen. 1002844. PubMed: 22876192.
-
(2012)
PLoS Genet
, vol.8
-
-
Yelina, N.E.1
Choi, K.2
Chelysheva, L.3
Macaulay, M.4
De Snoo, B.5
-
56
-
-
84859570036
-
Loss of DNA methylation affects the recombination landscape in Arabidopsis
-
doi:10.1073/pnas.1120841109. PubMed: 22451936
-
Mirouze M, Lieberman-Lazarovich M, Aversano R, Bucher E, Nicolet J et al. (2012) Loss of DNA methylation affects the recombination landscape in Arabidopsis. Proc Natl Acad Sci U S A 109: 5880-5885. doi:10.1073/pnas. 1120841109. PubMed: 22451936.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 5880-5885
-
-
Mirouze, M.1
Lieberman-Lazarovich, M.2
Aversano, R.3
Bucher, E.4
Nicolet, J.5
-
57
-
-
84867063134
-
Features of the Arabidopsis recombination landscape resulting from the combined loss of sequence variation and DNA methylation
-
doi:10.1073/pnas.1212955109. PubMed: 22988127
-
Colomé-Tatché M, Cortijo S, Wardenaar R, Morgado L, Lahouze B et al. (2012) Features of the Arabidopsis recombination landscape resulting from the combined loss of sequence variation and DNA methylation. Proc Natl Acad Sci U S A 109: 16240-16245. doi:10.1073/pnas.1212955109. PubMed: 22988127.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 16240-16245
-
-
Colomé-Tatché, M.1
Cortijo, S.2
Wardenaar, R.3
Morgado, L.4
Lahouze, B.5
-
58
-
-
84871438065
-
Tet1 controls meiosis by regulating meiotic gene expression
-
doi:10.1038/nature11709. PubMed: 23151479
-
Yamaguchi S, Hong K, Liu R, Shen L, Inoue A et al. (2012) Tet1 controls meiosis by regulating meiotic gene expression. Nature 492: 443-447. doi:10.1038/nature11709. PubMed: 23151479.
-
(2012)
Nature
, vol.492
, pp. 443-447
-
-
Yamaguchi, S.1
Hong, K.2
Liu, R.3
Shen, L.4
Inoue, A.5
-
59
-
-
0030937928
-
A drying-down technique for the spreading of mammalian meiocytes from the male and female germline
-
doi:10.1023/A:1018445520117. PubMed: 9088645
-
Peters AH, Plug AW, van Vugt MJ, de Boer P (1997) A drying-down technique for the spreading of mammalian meiocytes from the male and female germline. Chromosome Res 5: 66-68. doi:10.1023/A:1018445520117. PubMed: 9088645.
-
(1997)
Chromosome Res
, vol.5
, pp. 66-68
-
-
Peters, A.H.1
Plug, A.W.2
Van Vugt, M.J.3
De Boer, P.4
-
60
-
-
33751368660
-
Synaptic defects at meiosis I and non-obstructive azoospermia
-
doi:10.1093/humrep/del281. PubMed: 16861745
-
Topping D, Brown P, Judis L, Schwartz S, Seftel A et al. (2006) Synaptic defects at meiosis I and non-obstructive azoospermia. Hum Reprod 21: 3171-3177. doi:10.1093/humrep/del281. PubMed: 16861745.
-
(2006)
Hum Reprod
, vol.21
, pp. 3171-3177
-
-
Topping, D.1
Brown, P.2
Judis, L.3
Schwartz, S.4
Seftel, A.5
-
61
-
-
38349019812
-
Cohesin Smc1β determines meiotic chromatin axis loop organization
-
doi:10.1083/jcb.200706136. PubMed: 18180366
-
Novak I, Wang H, Revenkova E, Jessberger R, Scherthan H et al. (2008) Cohesin Smc1β determines meiotic chromatin axis loop organization. J Cell Biol 180: 83-90. doi:10.1083/jcb.200706136. PubMed: 18180366.
-
(2008)
J Cell Biol
, vol.180
, pp. 83-90
-
-
Novak, I.1
Wang, H.2
Revenkova, E.3
Jessberger, R.4
Scherthan, H.5
|