David C. Page, M.D. - Publications

Whitehead Institute (MIT), Cambridge, MA, United States 

144 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Kojima ML, de Rooij DG, Page DC. Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice. Elife. 8. PMID 30810530 DOI: 10.7554/eLife.43738  0.32
2018 Romer KA, de Rooij DG, Kojima ML, Page DC. Corrigendum to "Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting" [Dev. Biol. 443 (2018) 19-34]. Developmental Biology. PMID 30416000 DOI: 10.1016/j.ydbio.2018.10.021  0.32
2018 Romer KA, de Rooij DG, Kojima ML, Page DC. Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting. Developmental Biology. PMID 30149006 DOI: 10.1016/j.ydbio.2018.08.009  0.32
2017 Endo T, Freinkman E, de Rooij DG, Page DC. Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis. Proceedings of the National Academy of Sciences of the United States of America. PMID 29109271 DOI: 10.1073/pnas.1710837114  0.32
2017 Soh YQ, Mikedis MM, Kojima M, Godfrey AK, de Rooij DG, Page DC. Meioc maintains an extended meiotic prophase I in mice. Plos Genetics. 13: e1006704. PMID 28380054 DOI: 10.1371/journal.pgen.1006704  0.32
2016 Carmell MA, Dokshin GA, Skaletsky H, Hu YC, von Wolfswinkel JC, Igarashi KJ, Bellott DW, Nefedov M, Reddien PW, Enders GC, Uversky VN, Mello CC, Page DC. A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes. Elife. 5. PMID 27718356 DOI: 10.7554/eLife.19993  0.32
2016 Lesch BJ, Silber SJ, McCarrey JR, Page DC. Parallel evolution of male germline epigenetic poising and somatic development in animals. Nature Genetics. PMID 27294618 DOI: 10.1038/ng.3591  0.88
2015 Soh YQ, Junker JP, Gill ME, Mueller JL, van Oudenaarden A, Page DC. A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary. Plos Genetics. 11: e1005531. PMID 26378784 DOI: 10.1371/journal.pgen.1005531  0.88
2015 Yang F, Silber S, Leu NA, Oates RD, Marszalek JD, Skaletsky H, Brown LG, Rozen S, Page DC, Wang PJ. TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse. Embo Molecular Medicine. PMID 26136358 DOI: 10.15252/emmm.201404967  0.88
2015 Hughes JF, Skaletsky H, Koutseva N, Pyntikova T, Page DC. Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals. Genome Biology. 16: 104. PMID 26017895 DOI: 10.1186/s13059-015-0667-4  0.88
2015 Endo T, Romer KA, Anderson EL, Baltus AE, de Rooij DG, Page DC. Periodic retinoic acid-STRA8 signaling intersects with periodic germ-cell competencies to regulate spermatogenesis. Proceedings of the National Academy of Sciences of the United States of America. 112: E2347-56. PMID 25902548 DOI: 10.1073/pnas.1505683112  0.88
2015 Hu YC, Nicholls PK, Soh YQ, Daniele JR, Junker JP, van Oudenaarden A, Page DC. Licensing of primordial germ cells for gametogenesis depends on genital ridge signaling. Plos Genetics. 11: e1005019. PMID 25739037 DOI: 10.1371/journal.pgen.1005019  0.88
2014 Soh YQ, Alföldi J, Pyntikova T, Brown LG, Graves T, Minx PJ, Fulton RS, Kremitzki C, Koutseva N, Mueller JL, Rozen S, Hughes JF, Owens E, Womack JE, Murphy WJ, ... ... Page DC, et al. Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes. Cell. 159: 800-13. PMID 25417157 DOI: 10.1016/j.cell.2014.09.052  0.88
2014 Lesch BJ, Page DC. Poised chromatin in the mammalian germ line. Development (Cambridge, England). 141: 3619-26. PMID 25249456 DOI: 10.1242/dev.113027  0.88
2014 Koubova J, Hu YC, Bhattacharyya T, Soh YQ, Gill ME, Goodheart ML, Hogarth CA, Griswold MD, Page DC. Retinoic acid activates two pathways required for meiosis in mice. Plos Genetics. 10: e1004541. PMID 25102060 DOI: 10.1371/journal.pgen.1004541  0.88
2014 Bellott DW, Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Cho TJ, Koutseva N, Zaghlul S, Graves T, Rock S, Kremitzki C, Fulton RS, Dugan S, Ding Y, Morton D, ... ... Page DC, et al. Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators. Nature. 508: 494-9. PMID 24759411 DOI: 10.1038/nature13206  0.88
2013 Hughes JF, Skaletsky H, Bellott DW, Chowdhary BP, Warren WC, Worley KC, Wilson RK, Gibbs RA, Page DC. No bull: upholding community standards in public sharing of biological datasets. Proceedings of the National Academy of Sciences of the United States of America. 110: E4277. PMID 24173037 DOI: 10.1073/pnas.1315122110  0.88
2013 Lesch BJ, Dokshin GA, Young RA, McCarrey JR, Page DC. A set of genes critical to development is epigenetically poised in mouse germ cells from fetal stages through completion of meiosis. Proceedings of the National Academy of Sciences of the United States of America. 110: 16061-6. PMID 24043772 DOI: 10.1073/pnas.1315204110  0.88
2013 Hu YC, Okumura LM, Page DC. Gata4 is required for formation of the genital ridge in mice. Plos Genetics. 9: e1003629. PMID 23874227 DOI: 10.1371/journal.pgen.1003629  0.88
2013 Mueller JL, Skaletsky H, Brown LG, Zaghlul S, Rock S, Graves T, Auger K, Warren WC, Wilson RK, Page DC. Independent specialization of the human and mouse X chromosomes for the male germ line. Nature Genetics. 45: 1083-7. PMID 23872635 DOI: 10.1038/ng.2705  0.88
2013 Hu YC, de Rooij DG, Page DC. Tumor suppressor gene Rb is required for self-renewal of spermatogonial stem cells in mice. Proceedings of the National Academy of Sciences of the United States of America. 110: 12685-90. PMID 23858447 DOI: 10.1073/pnas.1311548110  0.88
2013 Dokshin GA, Baltus AE, Eppig JJ, Page DC. Oocyte differentiation is genetically dissociable from meiosis in mice. Nature Genetics. 45: 877-83. PMID 23770609 DOI: 10.1038/ng.2672  0.88
2013 Okumura LM, Lesch BJ, Page DC. The ligand binding domain of GCNF is not required for repression of pluripotency genes in mouse fetal ovarian germ cells. Plos One. 8: e66062. PMID 23762465 DOI: 10.1371/journal.pone.0066062  0.88
2013 Wang H, Hu YC, Markoulaki S, Welstead GG, Cheng AW, Shivalila CS, Pyntikova T, Dadon DB, Voytas DF, Bogdanove AJ, Page DC, Jaenisch R. TALEN-mediated editing of the mouse Y chromosome. Nature Biotechnology. 31: 530-2. PMID 23666012 DOI: 10.1038/nbt.2595  0.88
2013 Lange J, Noordam MJ, van Daalen SK, Skaletsky H, Clark BA, Macville MV, Page DC, Repping S. Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms. Genomics. 102: 257-64. PMID 23643616 DOI: 10.1016/j.ygeno.2013.04.018  0.88
2012 Rozen SG, Marszalek JD, Irenze K, Skaletsky H, Brown LG, Oates RD, Silber SJ, Ardlie K, Page DC. AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes. American Journal of Human Genetics. 91: 890-6. PMID 23103232 DOI: 10.1016/j.ajhg.2012.09.003  0.88
2012 Hughes JF, Skaletsky H, Page DC. Sequencing of rhesus macaque Y chromosome clarifies origins and evolution of the DAZ (Deleted in AZoospermia) genes. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 34: 1035-44. PMID 23055411 DOI: 10.1002/bies.201200066  0.88
2012 Lesch BJ, Page DC. Genetics of germ cell development. Nature Reviews. Genetics. 13: 781-94. PMID 23044825 DOI: 10.1038/nrg3294  0.88
2012 Buganim Y, Itskovich E, Hu YC, Cheng AW, Ganz K, Sarkar S, Fu D, Welstead GG, Page DC, Jaenisch R. Direct reprogramming of fibroblasts into embryonic Sertoli-like cells by defined factors. Cell Stem Cell. 11: 373-86. PMID 22958931 DOI: 10.1016/j.stem.2012.07.019  0.88
2012 Chen N, Bellott DW, Page DC, Clark AG. Identification of avian W-linked contigs by short-read sequencing. Bmc Genomics. 13: 183. PMID 22583744 DOI: 10.1186/1471-2164-13-183  0.88
2012 Heaney JD, Anderson EL, Michelson MV, Zechel JL, Conrad PA, Page DC, Nadeau JH. Germ cell pluripotency, premature differentiation and susceptibility to testicular teratomas in mice. Development (Cambridge, England). 139: 1577-86. PMID 22438569 DOI: 10.1242/dev.076851  0.88
2012 Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Graves T, Fulton RS, Dugan S, Ding Y, Buhay CJ, Kremitzki C, Wang Q, Shen H, Holder M, Villasana D, Nazareth LV, ... ... Page DC, et al. Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes. Nature. 483: 82-6. PMID 22367542 DOI: 10.1038/nature10843  0.88
2011 Medeiros LA, Dennis LM, Gill ME, Houbaviy H, Markoulaki S, Fu D, White AC, Kirak O, Sharp PA, Page DC, Jaenisch R. Mir-290-295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects. Proceedings of the National Academy of Sciences of the United States of America. 108: 14163-8. PMID 21844366 DOI: 10.1073/pnas.1111241108  0.88
2011 Dawlaty MM, Ganz K, Powell BE, Hu YC, Markoulaki S, Cheng AW, Gao Q, Kim J, Choi SW, Page DC, Jaenisch R. Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development. Cell Stem Cell. 9: 166-75. PMID 21816367 DOI: 10.1016/j.stem.2011.07.010  0.88
2011 Gill ME, Hu YC, Lin Y, Page DC. Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells. Proceedings of the National Academy of Sciences of the United States of America. 108: 7443-8. PMID 21504946 DOI: 10.1073/pnas.1104501108  0.88
2010 Bellott DW, Skaletsky H, Pyntikova T, Mardis ER, Graves T, Kremitzki C, Brown LG, Rozen S, Warren WC, Wilson RK, Page DC. Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition. Nature. 466: 612-6. PMID 20622855 DOI: 10.1038/nature09172  0.88
2010 Hughes JF, Skaletsky H, Pyntikova T, Graves TA, van Daalen SK, Minx PJ, Fulton RS, McGrath SD, Locke DP, Friedman C, Trask BJ, Mardis ER, Warren WC, Repping S, Rozen S, ... ... Page DC, et al. Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content. Nature. 463: 536-9. PMID 20072128 DOI: 10.1038/nature08700  0.88
2009 Bellott DW, Page DC. Reconstructing the evolution of vertebrate sex chromosomes. Cold Spring Harbor Symposia On Quantitative Biology. 74: 345-53. PMID 20508063 DOI: 10.1101/sqb.2009.74.048  0.88
2009 Rozen S, Marszalek JD, Alagappan RK, Skaletsky H, Page DC. Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection. American Journal of Human Genetics. 85: 923-8. PMID 20004767 DOI: 10.1016/j.ajhg.2009.11.011  0.88
2009 Lange J, Skaletsky H, van Daalen SK, Embry SL, Korver CM, Brown LG, Oates RD, Silber S, Repping S, Page DC. Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes. Cell. 138: 855-69. PMID 19737515 DOI: 10.1016/j.cell.2009.07.042  0.88
2008 Lin Y, Gill ME, Koubova J, Page DC. Germ cell-intrinsic and -extrinsic factors govern meiotic initiation in mouse embryos. Science (New York, N.Y.). 322: 1685-7. PMID 19074348 DOI: 10.1126/science.1166340  0.88
2008 Anderson EL, Baltus AE, Roepers-Gajadien HL, Hassold TJ, de Rooij DG, van Pelt AM, Page DC. Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 14976-80. PMID 18799751 DOI: 10.1073/pnas.0807297105  0.88
2008 Mueller JL, Mahadevaiah SK, Park PJ, Warburton PE, Page DC, Turner JM. The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression. Nature Genetics. 40: 794-9. PMID 18454149 DOI: 10.1038/ng.126  0.88
2008 Yang F, Gell K, van der Heijden GW, Eckardt S, Leu NA, Page DC, Benavente R, Her C, Höög C, McLaughlin KJ, Wang PJ. Meiotic failure in male mice lacking an X-linked factor. Genes & Development. 22: 682-91. PMID 18316482 DOI: 10.1101/gad.1613608  0.88
2008 Lange J, Skaletsky H, Bell GW, Page DC. MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome. Nucleic Acids Research. 36: D809-14. PMID 17965095 DOI: 10.1093/nar/gkm849  0.88
2007 Kimble J, Page DC. The mysteries of sexual identity. The germ cell's perspective. Science (New York, N.Y.). 316: 400-1. PMID 17446389 DOI: 10.1126/science.1142109  0.88
2007 Cheng Y, Buffone MG, Kouadio M, Goodheart M, Page DC, Gerton GL, Davidson I, Wang PJ. Abnormal sperm in mice lacking the Taf7l gene. Molecular and Cellular Biology. 27: 2582-9. PMID 17242199 DOI: 10.1128/MCB.01722-06  0.88
2006 Baltus AE, Menke DB, Hu YC, Goodheart ML, Carpenter AE, de Rooij DG, Page DC. In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication. Nature Genetics. 38: 1430-4. PMID 17115059 DOI: 10.1038/ng1919  0.88
2006 Hughes JF, Skaletsky H, Rozen S, Wilson RK, Page DC. Has the chimpanzee Y chromosome been sequenced? Nature Genetics. 38: 853-4; author reply . PMID 16874316 DOI: 10.1038/ng0806-853b  0.88
2006 Repping S, van Daalen SK, Brown LG, Korver CM, Lange J, Marszalek JD, Pyntikova T, van der Veen F, Skaletsky H, Page DC, Rozen S. High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nature Genetics. 38: 463-7. PMID 16501575 DOI: 10.1038/ng1754  0.88
2006 Koubova J, Menke DB, Zhou Q, Capel B, Griswold MD, Page DC. Retinoic acid regulates sex-specific timing of meiotic initiation in mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 2474-9. PMID 16461896 DOI: 10.1073/pnas.0510813103  0.88
2005 Lin Y, Page DC. Dazl deficiency leads to embryonic arrest of germ cell development in XY C57BL/6 mice. Developmental Biology. 288: 309-16. PMID 16310179 DOI: 10.1016/j.ydbio.2005.06.032  0.88
2005 Hughes JF, Skaletsky H, Pyntikova T, Minx PJ, Graves T, Rozen S, Wilson RK, Page DC. Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee. Nature. 437: 100-3. PMID 16136134 DOI: 10.1038/nature04101  0.88
2005 Wang PJ, Page DC, McCarrey JR. Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse. Human Molecular Genetics. 14: 2911-8. PMID 16118233 DOI: 10.1093/hmg/ddi322  0.88
2005 Pan J, Goodheart M, Chuma S, Nakatsuji N, Page DC, Wang PJ. RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis. Development (Cambridge, England). 132: 4029-39. PMID 16093322 DOI: 10.1242/dev.02003  0.88
2004 Repping S, Korver CM, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Are sequence family variants useful for identifying deletions in the human Y chromosome? American Journal of Human Genetics. 75: 514-7; author reply . PMID 15284951 DOI: 10.1086/423394  0.88
2004 Bradley J, Baltus A, Skaletsky H, Royce-Tolland M, Dewar K, Page DC. An X-to-autosome retrogene is required for spermatogenesis in mice. Nature Genetics. 36: 872-6. PMID 15258580 DOI: 10.1038/ng1390  0.88
2004 Repping S, van Daalen SK, Korver CM, Brown LG, Marszalek JD, Gianotten J, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics. 83: 1046-52. PMID 15177557 DOI: 10.1016/j.ygeno.2003.12.018  0.88
2004 Yao HH, Matzuk MM, Jorgez CJ, Menke DB, Page DC, Swain A, Capel B. Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 230: 210-5. PMID 15162500 DOI: 10.1002/dvdy.20042  0.88
2004 Natoli TA, Alberta JA, Bortvin A, Taglienti ME, Menke DB, Loring J, Jaenisch R, Page DC, Housman DE, Kreidberg JA. Wt1 functions in the development of germ cells in addition to somatic cell lineages of the testis. Developmental Biology. 268: 429-40. PMID 15063178 DOI: 10.1016/j.ydbio.2003.12.033  0.88
2004 Page DC. 2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome. American Journal of Human Genetics. 74: 399-402. PMID 15053010 DOI: 10.1086/382659  0.88
2004 Bortvin A, Goodheart M, Liao M, Page DC. Dppa3 / Pgc7 / stella is a maternal factor and is not required for germ cell specification in mice. Bmc Developmental Biology. 4: 2. PMID 15018652 DOI: 10.1186/1471-213X-4-2  0.88
2003 Menke DB, Koubova J, Page DC. Sexual differentiation of germ cells in XX mouse gonads occurs in an anterior-to-posterior wave. Developmental Biology. 262: 303-12. PMID 14550793 DOI: 10.1016/S0012-1606(03)00391-9  0.88
2003 Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nature Genetics. 35: 247-51. PMID 14528305 DOI: 10.1038/ng1250  0.88
2003 Tomasi PA, Oates R, Brown L, Delitala G, Page DC. The pituitary-testicular axis in Klinefelter's syndrome and in oligo-azoospermic patients with and without deletions of the Y chromosome long arm. Clinical Endocrinology. 59: 214-22. PMID 12864799 DOI: 10.1046/j.1365-2265.2003.01828.x  0.88
2003 Rozen S, Skaletsky H, Marszalek JD, Minx PJ, Cordum HS, Waterston RH, Wilson RK, Page DC. Abundant gene conversion between arms of palindromes in human and ape Y chromosomes. Nature. 423: 873-6. PMID 12815433 DOI: 10.1038/nature01723  0.88
2003 Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG, Repping S, Pyntikova T, Ali J, Bieri T, Chinwalla A, Delehaunty A, Delehaunty K, Du H, Fewell G, ... ... Page DC, et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature. 423: 825-37. PMID 12815422 DOI: 10.1038/nature01722  0.88
2003 Bortvin A, Eggan K, Skaletsky H, Akutsu H, Berry DL, Yanagimachi R, Page DC, Jaenisch R. Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei. Development (Cambridge, England). 130: 1673-80. PMID 12620990 DOI: 10.1242/dev.00366  0.88
2003 Phelan MC, Rogers RC, Crawford EC, Brown LG, Page DC. Velocardiofacial syndrome in an unexplained XX male. American Journal of Medical Genetics. Part A. 116: 77-9. PMID 12476456 DOI: 10.1002/ajmg.a.10833  0.88
2002 Menke DB, Page DC. Sexually dimorphic gene expression in the developing mouse gonad. Gene Expression Patterns : Gep. 2: 359-67. PMID 12617826 DOI: 10.1016/S1567-133X(02)00022-4  0.88
2002 Oates RD, Silber S, Brown LG, Page DC. Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI. Human Reproduction (Oxford, England). 17: 2813-24. PMID 12407032  0.88
2002 Repping S, Skaletsky H, Lange J, Silber S, Van Der Veen F, Oates RD, Page DC, Rozen S. Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure. American Journal of Human Genetics. 71: 906-22. PMID 12297986 DOI: 10.1086/342928  0.88
2002 Wang PJ, Page DC. Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis. Human Molecular Genetics. 11: 2341-6. PMID 12217962  0.88
2002 Lahn BT, Tang ZL, Zhou J, Barndt RJ, Parvinen M, Allis CD, Page DC. Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis. Proceedings of the National Academy of Sciences of the United States of America. 99: 8707-12. PMID 12072557 DOI: 10.1073/pnas.082248899  0.88
2001 Jaruzelska J, Korcz A, Wojda A, Jedrzejczak P, Bierla J, Surmacz T, Pawelczyk L, Page DC, Kotecki M. Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion. Journal of Medical Genetics. 38: 798-802. PMID 11732492  0.88
2001 Kuroda-Kawaguchi T, Skaletsky H, Brown LG, Minx PJ, Cordum HS, Waterston RH, Wilson RK, Silber S, Oates R, Rozen S, Page DC. The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nature Genetics. 29: 279-86. PMID 11687796 DOI: 10.1038/ng757  0.88
2001 Yang J, Bogerd HP, Wang PJ, Page DC, Cullen BR. Two closely related human nuclear export factors utilize entirely distinct export pathways. Molecular Cell. 8: 397-406. PMID 11545741 DOI: 10.1016/S1097-2765(01)00303-3  0.88
2001 Wang PJ, McCarrey JR, Yang F, Page DC. An abundance of X-linked genes expressed in spermatogonia. Nature Genetics. 27: 422-6. PMID 11279525 DOI: 10.1038/86927  0.88
2001 Tilford CA, Kuroda-Kawaguchi T, Skaletsky H, Rozen S, Brown LG, Rosenberg M, McPherson JD, Wylie K, Sekhon M, Kucaba TA, Waterston RH, Page DC. A physical map of the human Y chromosome. Nature. 409: 943-5. PMID 11237016 DOI: 10.1038/35057170  0.88
2000 Ion A, Crosby AH, Kremer H, Kenmochi N, Van Reen M, Fenske C, Van Der Burgt I, Brunner HG, Montgomery K, Kucherlapati RS, Patton MA, Page C, Mariman E, Jeffery S. Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2, DCN, EPS8, and RPL6. Journal of Medical Genetics. 37: 884-6. PMID 11185075  0.88
2000 Reijo RA, Dorfman DM, Slee R, Renshaw AA, Loughlin KR, Cooke H, Page DC. DAZ family proteins exist throughout male germ cell development and transit from nucleus to cytoplasm at meiosis in humans and mice. Biology of Reproduction. 63: 1490-6. PMID 11058556  0.88
2000 Sun C, Skaletsky H, Rozen S, Gromoll J, Nieschlag E, Oates R, Page DC. Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. Human Molecular Genetics. 9: 2291-6. PMID 11001932  0.88
2000 Giacalone J, Delobette S, Gibaja V, Ni L, Skiadas Y, Qi R, Edington J, Lai Z, Gebauer D, Zhao H, Anantharaman T, Mishra B, Brown LG, Saxena R, Page DC, et al. Optical mapping of BAC clones from the human Y chromosome DAZ locus. Genome Research. 10: 1421-9. PMID 10984460 DOI: 10.1101/gr.112100  0.88
2000 Bohossian HB, Skaletsky H, Page DC. Unexpectedly similar rates of nucleotide substitution found in male and female hominids. Nature. 406: 622-5. PMID 10949301 DOI: 10.1038/35020557  0.88
2000 Saxena R, de Vries JW, Repping S, Alagappan RK, Skaletsky H, Brown LG, Ma P, Chen E, Hoovers JM, Page DC. Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome. Genomics. 67: 256-67. PMID 10936047 DOI: 10.1006/geno.2000.6260  0.88
2000 Warren EH, Gavin MA, Simpson E, Chandler P, Page DC, Disteche C, Stankey KA, Greenberg PD, Riddell SR. The human UTY gene encodes a novel HLA-B8-restricted H-Y antigen. Journal of Immunology (Baltimore, Md. : 1950). 164: 2807-14. PMID 10679124  0.88
2000 Rocchietti-March M, Weinbauer GF, Page DC, Nieschlag E, Gromoll J. Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated. International Journal of Andrology. 23: 51-6. PMID 10632763 DOI: 10.1046/j.1365-2605.2000.00207.x  0.88
2000 Lahn BT, Page DC. A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins. Human Molecular Genetics. 9: 311-9. PMID 10607842  0.88
1999 Sun C, Skaletsky H, Birren B, Devon K, Tang Z, Silber S, Oates R, Page DC. An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y. Nature Genetics. 23: 429-32. PMID 10581029 DOI: 10.1038/70539  0.88
1999 Lahn BT, Page DC. Four evolutionary strata on the human X chromosome. Science (New York, N.Y.). 286: 964-7. PMID 10542153 DOI: 10.1126/science.286.5441.964  0.88
1999 Gromoll J, Weinbauer GF, Skaletsky H, Schlatt S, Rocchietti-March M, Page DC, Nieschlag E. The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome. Human Molecular Genetics. 8: 2017-24. PMID 10484770 DOI: 10.1093/hmg/8.11.2017  0.88
1999 Raymond CS, Parker ED, Kettlewell JR, Brown LG, Page DC, Kusz K, Jaruzelska J, Reinberg Y, Flejter WL, Bardwell VJ, Hirsch B, Zarkower D. A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. Human Molecular Genetics. 8: 989-96. PMID 10332030 DOI: 10.1093/hmg/8.6.989  0.88
1999 Lahn BT, Page DC. Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome. Nature Genetics. 21: 429-33. PMID 10192397 DOI: 10.1038/7771  0.88
1998 Silber SJ, Alagappan R, Brown LG, Page DC. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Human Reproduction (Oxford, England). 13: 3332-7. PMID 9886509 DOI: 10.1093/humrep/13.12.3332  0.88
1998 Railly PR, Page DC. We're off to see the genome Nature Genetics. 20: 15-17. PMID 9731523 DOI: 10.1038/1668  0.88
1998 Jegalian K, Page DC. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated Nature. 394: 776-780. PMID 9723615 DOI: 10.1038/29522  0.88
1998 Seligman J, Page DC. The Dazh gene is expressed in male and female embryonic gonads before germ cell sex differentiation Biochemical and Biophysical Research Communications. 245: 878-882. PMID 9588208 DOI: 10.1006/bbrc.1998.8530  0.88
1998 Kenmochi N, Kawaguchi T, Rozen S, Davis E, Goodman N, Hudson TJ, Tanaka T, Page DC. A map of 75 human ribosomal protein genes Genome Research. 8: 509-523. PMID 9582194  0.88
1998 Schwartz A, Chan DC, Brown LG, Alagappan R, Pettay D, Disteche C, McGillivray B, De La Chapelle A, Page DC. Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination Human Molecular Genetics. 7: 1-11. PMID 9384598 DOI: 10.1093/hmg/7.1.1  0.88
1997 Lahn BT, Page DC. Functional coherence of the human Y chromosome. Science (New York, N.Y.). 278: 675-80. PMID 9381176 DOI: 10.1126/science.278.5338.675  0.88
1997 Schiebel K, Winkelmann M, Mertz A, Xu X, Page DC, Weil D, Petit C, Rappold GA. Abnormal XY interchange between a novel isolated protein kinase gene, PRKY and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females Human Molecular Genetics. 6: 1985-1989. PMID 9302280 DOI: 10.1093/hmg/6.11.1985  0.88
1997 Page DC. Save the males! Nature Genetics. 17: 3. PMID 9288083 DOI: 10.1038/ng0997-3  0.88
1997 Luoh SW, Bain PA, Polakiewicz RD, Goodheart ML, Gardner H, Jaenisch R, Page DC. Zfx mutation results in small animal size and reduced germ cell number in male and female mice. Development (Cambridge, England). 124: 2275-84. PMID 9187153  0.88
1997 Mahaffey CL, Bayleran JK, Yeh GY, Lee TC, Page DC, Simpson EM. Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family Genomics. 41: 123-127. PMID 9126493 DOI: 10.1006/geno.1997.4611  0.88
1997 Menke DB, Mutter GL, Page DC. Expression of DAZ, an Azoospermia factor candidate, in human spermatogonia [5] American Journal of Human Genetics. 60: 237-241. PMID 8981970  0.88
1996 Saxena R, Brown LG, Hawkins T, Alagappan RK, Skaletsky H, Reeve MP, Reijo R, Rozen S, Dinulos MB, Disteche CM, Page DC. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned Nature Genetics. 14: 292-299. PMID 8896558  0.88
1996 Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, ... ... Page DC, et al. A gene map of the human genome. Science (New York, N.Y.). 274: 540-6. PMID 8849440 DOI: 10.1126/science.274.5287.540  0.88
1996 Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC. Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal. Nature Genetics. 14: 206-9. PMID 8841197 DOI: 10.1038/ng1096-206  0.88
1996 Reijo R, Seligman J, Dinulos MB, Jaffe T, Brown LG, Disteche CM, Page DC. Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty Genomics. 35: 346-352. PMID 8661148 DOI: 10.1006/geno.1996.0366  0.88
1996 Reijo R, Alagappan RK, Patrizio P, Page DC. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome Lancet. 347: 1290-1293. PMID 8622504 DOI: 10.1016/S0140-6736(96)90938-1  0.88
1996 Dietrich WF, Miller J, Steen R, Merchant MA, Damron-Boles D, Husain Z, Dredge R, Daly MJ, Ingalls KA, O'Connor TJ, Evans CA, DeAngelis MM, Levinson DM, Kruglyak L, Goodman N, ... ... Page DC, et al. A comprehensive genetic map of the mouse genome Nature. 380: 149-152. PMID 8600386 DOI: 10.1038/380149a0  0.88
1996 Reijo R, Lee TY, Salo P, Alagappan R, Brown LG, Rosenberg M, Rozen S, Jaffe T, Straus D, Hovatta O, De la Chapelle A, Silber S, Page DC, Edwards, Simpson. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Human Reproduction. 11: 27-54.  0.88
1995 Callen DF, Lane SA, Kozman H, Kremmidiotis G, Whitmore SA, Lowenstein M, Doggett NA, Kenmochi N, Page DC, Maglott DR, Nierman WC, Murakawa K, Berry R, Sikela JM, Houlgatte R, et al. Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: Demonstration of a 'hot spot' for recombination at 16p12 Genomics. 29: 503-511. PMID 8666401 DOI: 10.1006/geno.1995.9005  0.88
1995 LUOH SW, JEGALIAN K, LEE A, CHEN EY, RIDLEY A, PAGE DC. CpG Islands in HumanZFXandZFYand MouseZfxGenes: Sequence Similarities and Methylation Differences Genomics. 29: 353-363. PMID 8666382 DOI: 10.1006/geno.1995.9994  0.88
1995 Salo P, Kaariainen H, Petrovic V, Peltomaki P, Page DC, De la Chapelle A. Molecular mapping of the putative gonadoblastoma locus on the Y chromosome Genes Chromosomes and Cancer. 14: 210-214. PMID 8589038 DOI: 10.1002/gcc.2870140309  0.88
1995 Tsuchiya K, Reijo R, Page DC, Disteche CM. Gonadoblastoma: Molecular definition of the susceptibility region on the Y chromosome American Journal of Human Genetics. 57: 1400-1407. PMID 8533770  0.88
1995 Hudson TJ, Stein LD, Gerety SS, Ma J, Castle AB, Silva J, Slonim DK, Baptista R, Kruglyak L, Xu SH, Hu X, Colbert AM, Rosenberg C, Reeve-Daly MP, Rozen S, ... ... Page DC, et al. An STS-based map of the human genome. Science (New York, N.Y.). 270: 1945-54. PMID 8533086  0.88
1995 Salo P, Kääriäinen H, Page DC, de la Chapelle A. Deletion mapping of stature determinants on the long arm of the Y chromosome Human Genetics. 95: 283-286. PMID 7868119 DOI: 10.1007/BF00225194  0.88
1995 Polakiewicz RD, Munroe DJ, Sait SN, Tycowski KT, Nowak NJ, Shows TB, Housman DE, Page DC. Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. Genomics. 25: 577-80. PMID 7789996 DOI: 10.1016/0888-7543(95)80063-R  0.88
1995 Letterie GS, Page DC. Dysgerminoma and gonadal dysgenesis in a 46,XX female with no evidence of Y chromosomal DNA Gynecologic Oncology. 57: 423-425. PMID 7774849 DOI: 10.1006/gyno.1995.1166  0.88
1995 Chumakov HM, Rigault P, Le Gall I, Bellanné-Chantelot C, Billault A, Guillou S, Soularue P, Guasconi G, Poullier E, Gros I, Belova M, Sambucy JL, Susini L, Gervy P, Glibert F, ... ... Page DC, et al. A YAC contig map of the human genome Nature. 377: 175-183. PMID 7566096  0.88
1994 Luoh SW, Page DC. The Structure of the Zfx Gene on the Mouse X Chromosome Genomics. 19: 310-319. PMID 8188262 DOI: 10.1006/geno.1994.1063  0.88
1994 Zinn AR, Alagappan RK, Brown LG, Wool I, Page DC. Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes. Molecular and Cellular Biology. 14: 2485-92. PMID 8139551  0.88
1994 Bogan JS, Page DC. Ovary? Testis?-A mammalian dilemma Cell. 76: 603-607. PMID 8124705 DOI: 10.1016/0092-8674(94)90501-0  0.88
1994 Schmitt K, Lazzeroni LC, Foote S, Vollrath D, Fisher EMC, Goradia TM, Lange K, Page DC, Arnheim N. Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: Do double crossovers occur during male meiosis? American Journal of Human Genetics. 55: 423-430. PMID 8079986  0.88
1994 Zambrowicz BP, Zimmermann JW, Harendza CJ, Simpson EM, Page DC, Brinster RL, Palmiter RD. Expression of a mouse Zfy-1/lacZ transgene in the somatic cells of the embryonic gonad and germ cells of the adult testis. Development (Cambridge, England). 120: 1549-59. PMID 8050362  0.88
1994 Dietrich WF, Miller JC, Steen RG, Merchant M, Damron D, Nahf R, Gross A, Joyce DC, Wessel M, Dredge RD. A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nature Genetics. 7: 220-45. PMID 7920646 DOI: 10.1038/ng0694supp-220  0.88
1994 Page DC. Y chromosome sequences in Turner's syndrome and risk of gonadoblastoma or virilisation The Lancet. 343: 240. PMID 7904699 DOI: 10.1016/S0140-6736(94)91028-6  0.88
1994 Lahn BT, Ma N, Breg WR, Stratton R, Surti U, Page DC. Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Nature Genetics. 8: 243-50. PMID 7874166 DOI: 10.1038/ng1194-243  0.88
1994 Zambrowicz BP, Findley SD, Simpson EM, Page DC, Palmiter RD. Characterization of the murine Zfy1 and Zfy2 promoters. Genomics. 24: 406-8. PMID 7698773 DOI: 10.1006/geno.1994.1641  0.88
1994 Rosenfeld RG, Tesch LG, Rodriguez-Rigau LJ, McCauley E, Albertsson-Wikland K, Asch R, Cara J, Conte F, Hall JG, Lippe B, Nagel TC, Neely EK, Page DC, Ranke M, Saenger P, et al. Recommendations for diagnosis, treatment, and management of individuals with tumer syndrome Endocrinologist. 4: 351-358.  0.88
1993 Zinn AR, Page DC, Fisher EM. Turner syndrome: the case of the missing sex chromosome. Trends in Genetics : Tig. 9: 90-3. PMID 8488568 DOI: 10.1016/0168-9525(93)90230-F  0.88
1993 Watanabe M, Zinn AR, Page DC, Nishimoto T. Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome. Nature Genetics. 4: 268-71. PMID 8358435 DOI: 10.1038/ng0793-268  0.88
1993 Schmitt K, Vollralh D, Foote S, Fisher EMC, Page DC, Arnheim N. Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes Human Molecular Genetics. 2: 1978. PMID 8281166  0.88
1993 Behlke MA, Bogan JS, Beer-Romero P, Page DC. Evidence That the SRY Protein Is Encoded by a Single Exon on the Human Y Chromosome Genomics. 17: 736-739. PMID 8244390 DOI: 10.1006/geno.1993.1395  0.88
1992 Hamvas RMJ, Zinn A, Keer JT, Fisher EMC, Beer-Romero P, Brown SDM, Page DC. Rps4 maps near the inactivation center on the mouse X chromosome Genomics. 12: 363-367. PMID 1740345 DOI: 10.1016/0888-7543(92)90386-7  0.88
1992 Lindgren V, Chen Cp, Bryke CR, Lichter P, Page DC, Yang-Feng TL. Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes Human Genetics. 88: 393-398. PMID 1740316 DOI: 10.1007/BF00215672  0.88
1992 Cantrell MA, Bogan JS, Simpson E, Bicknell JN, Goulmy E, Chandler P, Pagon RA, Walker DC, Thuline HC, Graham JM. Deletion mapping of H-Y antigen to the long arm of the human Y chromosome. Genomics. 13: 1255-60. PMID 1505957 DOI: 10.1016/0888-7543(92)90043-R  0.88
1992 Vollrath D, Foote S, Hilton A, Brown LG, Beer-Romero P, Bogan JS, Page DC. The human Y chromosome: A 43-interval map based on naturally occurring deletions Science. 258: 52-59. PMID 1439769  0.88
1992 Foote S, Vollrath D, Hilton A, Page DC. The human Y chromosome: Overlapping DNA clones spanning the euchromatic region Science. 258: 60-66. PMID 1359640  0.88
1991 Adler DA, Bressler SL, Chapman VM, Page DC, Disteche CM. Inactivation of the Zfx gene on the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 88: 4592-5. PMID 2052543  0.88
1991 Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region American Journal of Human Genetics. 49: 253-260. PMID 1867189  0.88
1991 Simpson EM, Page DC. An interstitial deletion in mouse Y chromosomal DNA created a transcribed Zfy fusion gene Genomics. 11: 601-608. PMID 1774064 DOI: 10.1016/0888-7543(91)90067-O  0.88
1986 Vergnaud G, Page DC, Simmler MC, Brown L, Rouyer F, Noel B, Botstein D, de la Chapelle A, Weissenbach J. A deletion map of the human Y chromosome based on DNA hybridization. American Journal of Human Genetics. 38: 109-24. PMID 3004206  0.88
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