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1
Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice
Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice
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Deficiency of the Tbc1d21 gene causes male infertility with morphological abnormalities of the sperm mitochondria and flagellum in mice

PLoS genetics, 2020-09, Vol.16 (9), p.e1009020 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 Wang et al 2020 Wang et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1009020 ;PMID: 32976492

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2
Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice
Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice
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Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice

PLoS genetics, 2019-08, Vol.15 (8), p.e1008315-e1008315 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Moye et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Moye et al 2019 Moye et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008315 ;PMID: 31425546

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3
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility
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Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertility

PLoS genetics, 2018-08, Vol.14 (8), p.e1007602-e1007602 [Peer Reviewed Journal]

COPYRIGHT 2018 Public Library of Science ;COPYRIGHT 2018 Public Library of Science ;2018 Ta-Shma et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2018 Ta-Shma et al 2018 Ta-Shma et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1007602 ;PMID: 30148830

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4
Sperm acrosome overgrowth and infertility in mice lacking chromosome 18 pachytene piRNA
Sperm acrosome overgrowth and infertility in mice lacking chromosome 18 pachytene piRNA
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Sperm acrosome overgrowth and infertility in mice lacking chromosome 18 pachytene piRNA

PLoS genetics, 2021-04, Vol.17 (4), p.e1009485-e1009485 [Peer Reviewed Journal]

COPYRIGHT 2021 Public Library of Science ;This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1009485 ;PMID: 33831001

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5
Oligoasthenoteratozoospermia and infertility in mice deficient for miR-34b/c and miR-449 loci
Oligoasthenoteratozoospermia and infertility in mice deficient for miR-34b/c and miR-449 loci
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Oligoasthenoteratozoospermia and infertility in mice deficient for miR-34b/c and miR-449 loci

PLoS genetics, 2014-10, Vol.10 (10), p.e1004597-e1004597 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 O'Carroll et al 2014 O'Carroll et al ;2014 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Comazzetto S, Di Giacomo M, Rasmussen KD, Much C, Azzi C, Perlas E, et al. (2014) Oligoasthenoteratozoospermia and Infertility in Mice Deficient for miR-34b/c and miR-449 Loci. PLoS Genet 10(10): e1004597. doi:10.1371/journal.pgen.1004597 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1004597 ;PMID: 25329700

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6
The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans
The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans
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The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans

PLoS genetics, 2013-08, Vol.9 (8), p.e1003645-e1003645 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Wang et al 2013 Wang et al ;2013 Wang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Wang XN, Li ZS, Ren Y, Jiang T, Wang YQ, et al. (2013) The Wilms Tumor Gene, Wt1, Is Critical for Mouse Spermatogenesis via Regulation of Sertoli Cell Polarity and Is Associated with Non-Obstructive Azoospermia in Humans. PLoS Genet 9(8): e1003645. doi:10.1371/journal.pgen.1003645 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003645 ;PMID: 23935527

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7
HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse
HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse
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HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse

PLoS genetics, 2015-10, Vol.11 (10), p.e1005620-e1005620 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Lim et al 2015 Lim et al ;2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Lim SL, Qu ZP, Kortschak RD, Lawrence DM, Geoghegan J, Hempfling A-L, et al. (2015) HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse. PLoS Genet 11(10): e1005620. doi:10.1371/journal.pgen.1005620 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1005620 ;PMID: 26496356

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8
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1
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Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1

PLoS genetics, 2013-03, Vol.9 (3), p.e1003349 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Lopes et al 2013 Lopes et al ;2013 Lopes et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Lopes AM, Aston KI, Thompson E, Carvalho F, Gonçalves J, et al. (2013) Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1. PLoS Genet 9(3): e1003349. doi:10.1371/journal.pgen.1003349 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003349 ;PMID: 23555275

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9
A nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattle
A nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattle
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A nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattle

PLoS genetics, 2014-01, Vol.10 (1), p.e1004044-e1004044 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Pausch et al 2014 Pausch et al ;2014 Pausch et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Pausch H, Kölle S, Wurmser C, Schwarzenbacher H, Emmerling R, et al. (2014) A Nonsense Mutation in TMEM95 Encoding a Nondescript Transmembrane Protein Causes Idiopathic Male Subfertility in Cattle. PLoS Genet 10(1): e1004044. doi:10.1371/journal.pgen.1004044 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1004044 ;PMID: 24391514

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10
Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice
Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice
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Nexin-Dynein regulatory complex component DRC7 but not FBXL13 is required for sperm flagellum formation and male fertility in mice

PLoS genetics, 2020-01, Vol.16 (1), p.e1008585-e1008585 [Peer Reviewed Journal]

COPYRIGHT 2020 Public Library of Science ;COPYRIGHT 2020 Public Library of Science ;2020 Morohoshi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2020 Morohoshi et al 2020 Morohoshi et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008585 ;PMID: 31961863

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11
A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse
A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse
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A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse

PLoS genetics, 2012-09, Vol.8 (9), p.e1002900-e1002900 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;Cocquet et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Cocquet J, Ellis PJI, Mahadevaiah SK, Affara NA, Vaiman D, et al. (2012) A Genetic Basis for a Postmeiotic X Versus Y Chromosome Intragenomic Conflict in the Mouse. PLoS Genet 8(9): e1002900. doi:10.1371/journal.pgen.1002900 ;2012 Cocquet et al 2012 Cocquet et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002900 ;PMID: 23028340

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12
Partial deletion of chromosome 8 β-defensin cluster confers sperm dysfunction and infertility in male mice
Partial deletion of chromosome 8 β-defensin cluster confers sperm dysfunction and infertility in male mice
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Partial deletion of chromosome 8 β-defensin cluster confers sperm dysfunction and infertility in male mice

PLoS genetics, 2013-10, Vol.9 (10), p.e1003826 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;2013 Zhou et al 2013 Zhou et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003826 ;PMID: 24204287

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13
LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice
LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice
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LINE-1 Mediated Insertion into Poc1a (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice

PLoS genetics, 2015-10, Vol.11 (10), p.e1005569-e1005569 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Geister et al 2015 Geister et al ;2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: (Protein of Centriole 1 A) Causes Growth Insufficiency and Male Infertility in Mice. PLoS Genet 11(10): e1005569. doi:10.1371/journal.pgen.1005569 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1005569 ;PMID: 26496357

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14
Stability of the cytosine methylome during post-testicular sperm maturation in mouse
Stability of the cytosine methylome during post-testicular sperm maturation in mouse
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Stability of the cytosine methylome during post-testicular sperm maturation in mouse

PLoS genetics, 2021-03, Vol.17 (3), p.e1009416-e1009416 [Peer Reviewed Journal]

COPYRIGHT 2021 Public Library of Science ;COPYRIGHT 2021 Public Library of Science ;2021 Galan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 Galan et al 2021 Galan et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1009416 ;PMID: 33661909

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15
The meiotic nuclear lamina regulates chromosome dynamics and promotes efficient homologous recombination in the mouse
The meiotic nuclear lamina regulates chromosome dynamics and promotes efficient homologous recombination in the mouse
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The meiotic nuclear lamina regulates chromosome dynamics and promotes efficient homologous recombination in the mouse

PLoS genetics, 2013-01, Vol.9 (1), p.e1003261-e1003261 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Link et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Link J, Jahn D, Schmitt J, Göb E, Baar J, et al. (2013) The Meiotic Nuclear Lamina Regulates Chromosome Dynamics and Promotes Efficient Homologous Recombination in the Mouse. PLoS Genet 9(1): e1003261. doi:10.1371/journal.pgen.1003261 ;2013 Link et al 2013 Link et al ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003261 ;PMID: 23382700

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16
Y fuse? Sex chromosome fusions in fishes and reptiles
Y fuse? Sex chromosome fusions in fishes and reptiles
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Y fuse? Sex chromosome fusions in fishes and reptiles

PLoS genetics, 2015-05, Vol.11 (5), p.e1005237 [Peer Reviewed Journal]

COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Pennell et al 2015 Pennell et al ;2015 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Pennell MW, Kirkpatrick M, Otto SP, Vamosi JC, Peichel CL, Valenzuela N, et al. (2015) Y Fuse? Sex Chromosome Fusions in Fishes and Reptiles. PLoS Genet 11(5): e1005237. doi:10.1371/journal.pgen.1005237 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1005237 ;PMID: 25993542

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17
Recombination in the human Pseudoautosomal region PAR1
Recombination in the human Pseudoautosomal region PAR1
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Recombination in the human Pseudoautosomal region PAR1

PLoS genetics, 2014-07, Vol.10 (7), p.e1004503-e1004503 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Hinch et al 2014 Hinch et al ;2014 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hinch AG, Altemose N, Noor N, Donnelly P, Myers SR (2014) Recombination in the Human Pseudoautosomal Region PAR1. PLoS Genet 10(7): e1004503. doi:10.1371/journal.pgen.1004503 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1004503 ;PMID: 25033397

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18
Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes
Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes
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Acute versus chronic loss of mammalian Azi1/Cep131 results in distinct ciliary phenotypes

PLoS genetics, 2013-12, Vol.9 (12), p.e1003928-e1003928 [Peer Reviewed Journal]

COPYRIGHT 2013 Public Library of Science ;COPYRIGHT 2013 Public Library of Science ;2013 Hall et al 2013 Hall et al ;2013 Hall et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hall EA, Keighren M, Ford MJ, Davey T, Jarman AP, et al. (2013) Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes. PLoS Genet 9(12): e1003928. doi:10.1371/journal.pgen.1003928 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1003928 ;PMID: 24415959

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19
Two-By-One model of cytoplasmic incompatibility: Synthetic recapitulation by transgenic expression of cifA and cifB in Drosophila
Two-By-One model of cytoplasmic incompatibility: Synthetic recapitulation by transgenic expression of cifA and cifB in Drosophila
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Two-By-One model of cytoplasmic incompatibility: Synthetic recapitulation by transgenic expression of cifA and cifB in Drosophila

PLoS genetics, 2019-06, Vol.15 (6), p.e1008221-e1008221 [Peer Reviewed Journal]

COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Shropshire, Bordenstein. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Shropshire, Bordenstein 2019 Shropshire, Bordenstein ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1008221 ;PMID: 31242186

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20
DNA methylation of the gonadal aromatase (cyp19a) promoter is involved in temperature-dependent sex ratio shifts in the European sea bass
DNA methylation of the gonadal aromatase (cyp19a) promoter is involved in temperature-dependent sex ratio shifts in the European sea bass
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DNA methylation of the gonadal aromatase (cyp19a) promoter is involved in temperature-dependent sex ratio shifts in the European sea bass

PLoS genetics, 2011-12, Vol.7 (12), p.e1002447-e1002447 [Peer Reviewed Journal]

COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;Navarro-Martín et al. 2011 ;2011 Navarro-Martín et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Navarro-Martín L, Viñas J, Ribas L, Díaz N, Gutiérrez A, et al. (2011) DNA Methylation of the Gonadal Aromatase (cyp19a) Promoter Is Involved in Temperature-Dependent Sex Ratio Shifts in the European Sea Bass. PLoS Genet 7(12): e1002447. doi:10.1371/journal.pgen.1002447 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002447 ;PMID: 22242011

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