References analysis of the Wikipedia article "Inactivación do cromosoma X" in the Galician version

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Gartler SM, Varadarajan KR, Luo P, Canfield TK, Traynor J, Francke U, Hansen RS (September 2004). "Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins". BMC Biology 2: 21. PMC 521681. PMID 15377381. doi:10.1186/1741-7007-2-21.

Reinius B, Shi C, Hengshuo L, Sandhu KS, Radomska KJ, Rosen GD, Lu L, Kullander K, Williams RW, Jazin E (November 2010). "Female-biased expression of long non-coding RNAs in domains that escape X-inactivation in mouse". BMC Genomics 11: 614. PMC 3091755. PMID 21047393. doi:10.1186/1471-2164-11-614.

Ohno S, Kaplan WD, Kinosita R (October 1959). "Formation of the sex chromatin by a single X-chromosome in liver cells of Rattus norvegicus". Experimental Cell Research 18 (2): 415–8. PMID 14428474. doi:10.1016/0014-4827(59)90031-X.

Lyon MF (April 1961). "Gene action in the X-chromosome of the mouse (Mus musculus L.)". Nature 190 (4773): 372–3. Bibcode:1961Natur.190..372L. PMID 13764598. doi:10.1038/190372a0.

Beutler E (January 2008). "Glucose-6-phosphate dehydrogenase deficiency: a historical perspective". Blood 111 (1): 16–24. PMID 18156501. doi:10.1182/blood-2007-04-077412.

Beutler E, Yeh M, Fairbanks VF (January 1962). "The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker". Proceedings of the National Academy of Sciences of the United States of America 48 (1): 9–16. Bibcode:1962PNAS...48....9B. PMC 285481. PMID 13868717. doi:10.1073/pnas.48.1.9.

Takagi N, Sasaki M (August 1975). "Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse". Nature 256 (5519): 640–2. Bibcode:1975Natur.256..640T. PMID 1152998. doi:10.1038/256640a0.

Cheng MK, Disteche CM (August 2004). "Silence of the fathers: early X inactivation". BioEssays 26 (8): 821–4. PMID 15273983. doi:10.1002/bies.20082. (require subscrición (?)).

Okamoto I, Otte AP, Allis CD, Reinberg D, Heard E (January 2004). "Epigenetic dynamics of imprinted X inactivation during early mouse development". Science 303 (5658): 644–9. Bibcode:2004Sci...303..644O. PMID 14671313. doi:10.1126/science.1092727.

Deng Q, Ramsköld D, Reinius B, Sandberg R (January 2014). "Single-cell RNA-seq reveals dynamic, random monoallelic gene expression in mammalian cells". Science 343 (6167): 193–6. Bibcode:2014Sci...343..193D. PMID 24408435. doi:10.1126/science.1245316.

Xue Z, Huang K, Cai C, Cai L, Jiang CY, Feng Y, Liu Z, Zeng Q, Cheng L, Sun YE, Liu JY, Horvath S, Fan G (August 2013). "Genetic programs in human and mouse early embryos revealed by single-cell RNA sequencing". Nature (en inglés) 500 (7464): 593–7. Bibcode:2013Natur.500..593X. PMC 4950944. PMID 23892778. doi:10.1038/nature12364.

Borensztein M, Syx L, Ancelin K, Diabangouaya P, Picard C, Liu T, Liang JB, Vassilev I, Galupa R, Servant N, Barillot E, Surani A, Chen CJ, Heard E (March 2017). "Xist-dependent imprinted X inactivation and the early developmental consequences of its failure". Nature Structural & Molecular Biology (en inglés) 24 (3): 226–233. PMC 5337400. PMID 28134930. doi:10.1038/nsmb.3365.

Deng X, Berletch JB, Nguyen DK, Disteche CM (June 2014). "X chromosome regulation: diverse patterns in development, tissues and disease". Nature Reviews. Genetics (en inglés) 15 (6): 367–78. PMC 4117651. PMID 24733023. doi:10.1038/nrg3687.

Vértesy Á, Arindrarto W, Roost MS, Reinius B, Torrens-Juaneda V, Bialecka M, et al. (May 2018). "Parental haplotype-specific single-cell transcriptomics reveal incomplete epigenetic reprogramming in human female germ cells". Nature Communications (en inglés) 9 (1): 1873. Bibcode:2018NatCo...9.1873V. PMC 5951918. PMID 29760424. doi:10.1038/s41467-018-04215-7.

Guo F, Yan L, Guo H, Li L, Hu B, Zhao Y, et al. (June 2015). "The Transcriptome and DNA Methylome Landscapes of Human Primordial Germ Cells". Cell 161 (6): 1437–52. PMID 26046443. doi:10.1016/j.cell.2015.05.015.

Puck JM, Willard HF (January 1998). "X inactivation in females with X-linked disease". The New England Journal of Medicine 338 (5): 325–8. PMID 9445416. doi:10.1056/NEJM199801293380611.

Balaton BP, Cotton AM, Brown CJ (30 December 2015). "Derivation of consensus inactivation status for X-linked genes from genome-wide studies". Biology of Sex Differences 6 (35): 35. PMC 4696107. PMID 26719789. doi:10.1186/s13293-015-0053-7.

Graves JA (1996). "Mammals that break the rules: genetics of marsupials and monotremes". Annual Review of Genetics 30: 233–60. PMID 8982455. doi:10.1146/annurev.genet.30.1.233.

Lyon MF (January 1972). "X-chromosome inactivation and developmental patterns in mammals". Biological Reviews of the Cambridge Philosophical Society 47 (1): 1–35. PMID 4554151. doi:10.1111/j.1469-185X.1972.tb00969.x.

Connallon T, Clark AG (April 2013). "Sex-differential selection and the evolution of X inactivation strategies". PLoS Genetics 9 (4): e1003440. PMC 3630082. PMID 23637618. doi:10.1371/journal.pgen.1003440.

Ma L, Hoffman G, Keinan A (March 2015). "X-inactivation informs variance-based testing for X-linked association of a quantitative trait". BMC Genomics 16: 241. PMC 4381508. PMID 25880738. doi:10.1186/s12864-015-1463-y.

Habekost CT, Pereira FS, Vargas CR, Coelho DM, Torrez V, Oses JP, Portela LV, Schestatsky P, Felix VT, Matte U, Torman VL, Jardim LB (October 2015). "Progression rate of myelopathy in X-linked adrenoleukodystrophy heterozygotes". Metabolic Brain Disease 30 (5): 1279–84. PMID 25920484. doi:10.1007/s11011-015-9672-2.

Holle JR, Marsh RA, Holdcroft AM, Davies SM, Wang L, Zhang K, Jordan MB (July 2015). "Hemophagocytic lymphohistiocytosis in a female patient due to a heterozygous XIAP mutation and skewed X chromosome inactivation". Pediatric Blood & Cancer 62 (7): 1288–90. PMID 25801017. doi:10.1002/pbc.25483.

Burgemeister AL, Zirn B, Oeffner F, Kaler SG, Lemm G, Rossier E, Büttel HM (November 2015). "Menkes disease with discordant phenotype in female monozygotic twins". American Journal of Medical Genetics. Part A 167A (11): 2826–9. PMID 26239182. doi:10.1002/ajmg.a.37276.

Brioschi S, Gualandi F, Scotton C, Armaroli A, Bovolenta M, Falzarano MS, Sabatelli P, Selvatici R, D'Amico A, Pane M, Ricci G, Siciliano G, Tedeschi S, Pini A, Vercelli L, De Grandis D, Mercuri E, Bertini E, Merlini L, Mongini T, Ferlini A (August 2012). "Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype". BMC Medical Genetics 13: 73. PMC 3459813. PMID 22894145. doi:10.1186/1471-2350-13-73.

Lee JT, Jaenisch R (March 1997). "Long-range cis effects of ectopic X-inactivation centres on a mouse autosome". Nature 386 (6622): 275–9. Bibcode:1997Natur.386..275L. PMID 9069285. doi:10.1038/386275a0.

Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre". Nature Genetics 21 (4): 400–4. PMID 10192391. doi:10.1038/7734.

Hoki Y, Kimura N, Kanbayashi M, Amakawa Y, Ohhata T, Sasaki H, Sado T (January 2009). "A proximal conserved repeat in the Xist gene is essential as a genomic element for X-inactivation in mouse". Development 136 (1): 139–46. PMID 19036803. doi:10.1242/dev.026427.

Penny GD, Kay GF, Sheardown SA, Rastan S, Brockdorff N (1996). "Requirement for Xist in X chromosome inactivation". Nature 379 (6561): 131–7. Bibcode:1996Natur.379..131P. PMID 8538762. doi:10.1038/379131a0. Erro no estilo Vancouver: wikilink (Axuda)

Herzing LB, Romer JT, Horn JM, Ashworth A (March 1997). "Xist has properties of the X-chromosome inactivation centre". Nature 386 (6622): 272–5. Bibcode:1997Natur.386..272H. PMID 9069284. doi:10.1038/386272a0.

Ng K, Pullirsch D, Leeb M, Wutz A (January 2007). "Xist and the order of silencing" (Review Article). EMBO Reports 8 (1): 34–9. PMC 1796754. PMID 17203100. doi:10.1038/sj.embor.7400871. Table 1 Features of the inactive X territory – Orixinado de;
Chow JC, Yen Z, Ziesche SM, Brown CJ (2005). "Silencing of the mammalian X chromosome". Annual Review of Genomics and Human Genetics 6: 69–92. PMID 16124854. doi:10.1146/annurev.genom.6.080604.162350.
Lucchesi JC, Kelly WG, Panning B (2005). "Chromatin remodeling in dosage compensation". Annual Review of Genetics 39: 615–51. PMID 16285873. doi:10.1146/annurev.genet.39.073003.094210.

Veneti Z, Gkouskou KK, Eliopoulos AG (July 2017). "Polycomb Repressor Complex 2 in Genomic Instability and Cancer". Int J Mol Sci 18 (8). PMC 5578047. PMID 28758948. doi:10.3390/ijms18081657.

Costanzi C, Pehrson JR (June 1998). "Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals". Nature 393 (6685): 599–601. Bibcode:1998Natur.393..599C. PMID 9634239. doi:10.1038/31275.

Barr ML, Bertram EG (April 1949). "A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis". Nature 163 (4148): 676–677. Bibcode:1949Natur.163..676B. PMID 18120749. doi:10.1038/163676a0.

Plath K, Mlynarczyk-Evans S, Nusinow DA, Panning B (2002). "Xist RNA and the mechanism of X chromosome inactivation". Annual Review of Genetics 36: 233–78. PMID 12429693. doi:10.1146/annurev.genet.36.042902.092433.

Carrel L, Willard HF (March 2005). "X-inactivation profile reveals extensive variability in X-linked gene expression in females". Nature 434 (7031): 400–4. Bibcode:2005Natur.434..400C. PMID 15772666. doi:10.1038/nature03479.

Calabrese JM, Sun W, Song L, Mugford JW, Williams L, Yee D, Starmer J, Mieczkowski P, Crawford GE, Magnuson T (November 2012). "Site-specific silencing of regulatory elements as a mechanism of X inactivation". Cell 151 (5): 951–63. PMC 3511858. PMID 23178118. doi:10.1016/j.cell.2012.10.037.

Yang F, Babak T, Shendure J, Disteche CM (May 2010). "Global survey of escape from X inactivation by RNA-sequencing in mouse". Genome Research 20 (5): 614–22. PMC 2860163. PMID 20363980. doi:10.1101/gr.103200.109.

Berletch JB, Yang F, Disteche CM (June 2010). "Escape from X inactivation in mice and humans". Genome Biology 11 (6): 213. PMC 2911101. PMID 20573260. doi:10.1186/gb-2010-11-6-213.

Linder D, Gartler SM (October 1965). "Glucose-6-phosphate dehydrogenase mosaicism: utilization as a cell marker in the study of leiomyomas". Science 150 (3692): 67–9. Bibcode:1965Sci...150...67L. PMID 5833538. doi:10.1126/science.150.3692.67.

Parsons BL (2008). "Many different tumor types have polyclonal tumor origin: evidence and implications". Mutation Research 659 (3): 232–47. PMID 18614394. doi:10.1016/j.mrrev.2008.05.004.

Chen GL, Prchal JT (September 2007). "X-linked clonality testing: interpretation and limitations". Blood 110 (5): 1411–9. PMC 1975831. PMID 17435115. doi:10.1182/blood-2006-09-018655.

Petersson F, Branzovsky J, Martinek P, Korabecna M, Kruslin B, Hora M, et al. (July 2014). "The leiomyomatous stroma in renal cell carcinomas is polyclonal and not part of the neoplastic process". Virchows Archiv 465 (1): 89–96. PMID 24838683. doi:10.1007/s00428-014-1591-9.

Comertpay S, Pastorino S, Tanji M, Mezzapelle R, Strianese O, Napolitano A, Baumann F, Weigel T, Friedberg J, Sugarbaker P, Krausz T, Wang E, Powers A, Gaudino G, Kanodia S, Pass HI, Parsons BL, Yang H, Carbone M (December 2014). "Evaluation of clonal origin of malignant mesothelioma". Journal of Translational Medicine 12: 301. PMC 4255423. PMID 25471750. doi:10.1186/s12967-014-0301-3.

Jiang J, Jing Y, Cost GJ, Chiang JC, Kolpa HJ, Cotton AM, et al. (August 2013). "Translating dosage compensation to trisomy 21". Nature 500 (7462): 296–300. Bibcode:2013Natur.500..296J. PMC 3848249. PMID 23863942. doi:10.1038/nature12394.

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Lyon MF (April 1961). "Gene action in the X-chromosome of the mouse (Mus musculus L.)". Nature 190 (4773): 372–3. Bibcode:1961Natur.190..372L. PMID 13764598. doi:10.1038/190372a0.

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ncbi.nlm.nih.gov

Lyon MF (April 1961). "Gene action in the X-chromosome of the mouse (Mus musculus L.)". Nature 190 (4773): 372–3. Bibcode:1961Natur.190..372L. PMID 13764598. doi:10.1038/190372a0.

Beutler E (January 2008). "Glucose-6-phosphate dehydrogenase deficiency: a historical perspective". Blood 111 (1): 16–24. PMID 18156501. doi:10.1182/blood-2007-04-077412.

Cheng MK, Disteche CM (August 2004). "Silence of the fathers: early X inactivation". BioEssays 26 (8): 821–4. PMID 15273983. doi:10.1002/bies.20082. (require subscrición (?)).

Puck JM, Willard HF (January 1998). "X inactivation in females with X-linked disease". The New England Journal of Medicine 338 (5): 325–8. PMID 9445416. doi:10.1056/NEJM199801293380611.

Graves JA (1996). "Mammals that break the rules: genetics of marsupials and monotremes". Annual Review of Genetics 30: 233–60. PMID 8982455. doi:10.1146/annurev.genet.30.1.233.

Barakat TS, Gribnau J (2010). "X Chromosome Inactivation and Embryonic Stem Cells". En Meshorer E, Plath K. The Cell Biology of Stem Cells. Landes Bioscience and Springer Science+Business Media.

Belmont JW (June 1996). "Genetic control of X inactivation and processes leading to X-inactivation skewing". American Journal of Human Genetics 58 (6): 1101–8. PMC 1915050. PMID 8651285.

Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre". Nature Genetics 21 (4): 400–4. PMID 10192391. doi:10.1038/7734.

Veneti Z, Gkouskou KK, Eliopoulos AG (July 2017). "Polycomb Repressor Complex 2 in Genomic Instability and Cancer". Int J Mol Sci 18 (8). PMC 5578047. PMID 28758948. doi:10.3390/ijms18081657.

Costanzi C, Stein P, Worrad DM, Schultz RM, Pehrson JR (June 2000). "Histone macroH2A1 is concentrated in the inactive X chromosome of female preimplantation mouse embryos" (PDF). Development 127 (11): 2283–9. PMID 10804171.

Berletch JB, Yang F, Disteche CM (June 2010). "Escape from X inactivation in mice and humans". Genome Biology 11 (6): 213. PMC 2911101. PMID 20573260. doi:10.1186/gb-2010-11-6-213.

Parsons BL (2008). "Many different tumor types have polyclonal tumor origin: evidence and implications". Mutation Research 659 (3): 232–47. PMID 18614394. doi:10.1016/j.mrrev.2008.05.004.

Chen GL, Prchal JT (September 2007). "X-linked clonality testing: interpretation and limitations". Blood 110 (5): 1411–9. PMC 1975831. PMID 17435115. doi:10.1182/blood-2006-09-018655.

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Inactivación do cromosoma X (Galician Wikipedia)

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