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La ricerca find articoli where soggetti phrase all words 'X chromosome inactivation' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 493 riferimenti
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    1. Ostrer, H
      Genome and hormones: Gender differences in physiology - Invited review: Sex-based differences in gene expression

      JOURNAL OF APPLIED PHYSIOLOGY
    2. Brown, CJ
      Equality of the sexes: Mammalian dosage compensation

      SEMINARS IN REPRODUCTIVE MEDICINE
    3. Robinson, WP; Beever, C; Brown, CJ; Stephenson, MD
      Skewed X inactivation and recurrent spontaneous abortion

      SEMINARS IN REPRODUCTIVE MEDICINE
    4. Uehara, S; Sato, K; Hashiyada, M; Obara, Y; Matsuzaki, S; Nata, M; Okamura, K
      X chromosome inactivation patterns in 45,X/46,XX mosaics

      JOURNAL OF HUMAN GENETICS
    5. Erdmann, VA; Barciszewska, MZ; Hochberg, A; de Groot, N; Barciszewski, J
      Regulatory RNAs

      CELLULAR AND MOLECULAR LIFE SCIENCES
    6. Vasques, LR; Pereira, LV
      Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs)

      DNA RESEARCH
    7. Nesterova, TB; Slobodyanyuk, SY; Elisaphenko, EA; Shevchenko, AI; Johnston, C; Pavlova, ME; Rogozin, IB; Kolesnikov, NN; Brockdorff, N; Zakian, SM
      Characterization of the genomic Xist locus in rodents reveals conservationof overall gene structure and tandem repeats but rapid evolution of uniquesequence

      GENOME RESEARCH
    8. Paulsen, M; Takada, S; Youngson, NA; Benchaib, M; Charlier, C; Segers, K; Georges, M; Ferguson-Smith, AC
      Comparative sequence analysis of the imprinted Dlk1-Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2-H19 region

      GENOME RESEARCH
    9. Urnov, FD; Wolffe, AP
      Above and within the genome: Epigenetics past and present

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    10. Fischer, A
      Primary T-lymphocyte immunodeficiencies

      CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
    11. Jungbluth, AA; King, R; Fisher, DE; Iversen, K; Coplan, K; Kolb, D; Williamson, B; Chen, YT; Stockert, E; Old, LJ; Busam, KJ
      Immunohistochemical and reverse transcription-polymerase chain reaction expression analysis of tyrosinase and microphthalmia-associated transcriptionfactor in angiomyolipomas

      APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY
    12. Diaz-Cano, SJ; Blanes, A; Wolfe, HJ
      PCR techniques for clonality assays

      DIAGNOSTIC MOLECULAR PATHOLOGY
    13. Levy, A
      Monoclonality of endocrine tumours: what does it mean?

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    14. Girard, M; Couvert, P; Carrie, A; Tardieu, M; Chelly, J; Beldjord, C; Bienvenu, T
      Parental origin of de novo MECP2 mutations in Rett syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    15. LaSalle, JM; Goldstine, J; Balmer, D; Greco, CM
      Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

      HUMAN MOLECULAR GENETICS
    16. Wan, MM; Zhao, KJ; Lee, SSJ; Francke, U
      MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome

      HUMAN MOLECULAR GENETICS
    17. Ellaway, C; Christodoulou, J
      Rett syndrome: clinical characteristics and recent genetic advances

      DISABILITY AND REHABILITATION
    18. Romero, NB; De Lonlay, P; Llense, S; Leturcq, F; Touati, G; Urtizberea, JA; Saudubray, JM; Munnich, A; Kaplan, JC; Recan, D
      Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomaticcarrier with 'de novo' duplication of dystrophin gene

      NEUROMUSCULAR DISORDERS
    19. Chen, TC; Chou, TB; Ng, KF; Hsieh, LL; Chou, YHW
      Hepatocellular carcinoma associated with focal nodular hyperplasia - Report of a case with clonal analysis

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    20. Karasawa, M; Tsukamoto, N; Yamane, A; Okamoto, K; Maehara, T; Yokohama, A; Nojima, Y; Omine, M
      Analysis of the distribution of CAG repeats and X-chromosome inactivation status of HUMARA gene in healthy female subjects using improved fluorescence-based assay

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    21. Boultwood, J; Wainscoat, JS
      Clonality in the myelodysplastic syndromes

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    22. Tefferi, A
      The pathogenesis of chronic myeloproliferative diseases

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    23. Guo, ZM; Wu, F; Asplund, A; Hu, XR; Mazurenko, N; Kisseljov, F; Ponten, J; Wilander, E
      Analysis of intratumoral heterogeneity of chromosome 3p deletions and genetic evidence of polyclonal origin of cervical squamous carcinoma

      MODERN PATHOLOGY
    24. Tada, T; Tada, M
      Toti-/pluripotential stem cells and epigenetic modifications

      CELL STRUCTURE AND FUNCTION
    25. Gringras, P; Chen, W
      Mechanisms for differences in monozygous twins

      EARLY HUMAN DEVELOPMENT
    26. Memili, E; Hong, YK; Kim, DH; Ontiveros, SD; Strauss, WM
      Murine Xist RNA isoforms are different at their 3 ' ends: a role for differential polyadenylation

      GENE
    27. Ishihara, H; Kanda, F; Nishio, H; Sumino, K; Chihara, K
      Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy

      JOURNAL OF NEUROLOGY
    28. Solari, AJ; Rahn, IM; Ferreyra, ME; Carballo, MA
      The behavior of sex chromosomes in two human X-autosome translocations: Failure of extensive x-inactivation spreading

      BIOCELL
    29. Monk, M; Salpekar, A
      Expression of imprinted genes in human preimplantation development

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    30. Hui, P; Perkins, AS; Glusac, EJ
      Assessment of clonality in melanocytic nevi

      JOURNAL OF CUTANEOUS PATHOLOGY
    31. Shih, LY; Lin, TL; Dunn, P; Wu, JH; Tseng, CP; Lai, CL; Wang, PN; Kuo, MC
      Clonality analysis using X-chromosome inactivation patterns by HUMARA-PCR assay in female controls and patients with idiopathic thrombocytosis in Taiwan

      EXPERIMENTAL HEMATOLOGY
    32. Van Pottelbergh, I; Lumbroso, S; Goemaere, S; Sultan, C; Kaufman, JM
      Lack of influence of the androgen receptor gene CAG-repeat polymorphism onsex steroid status and bone metabolism in elderly men

      CLINICAL ENDOCRINOLOGY
    33. Luikenhuis, S; Wutz, A; Jaenisch, R
      Antisense transcription through the Xist locus mediates Tsix function in embryonic stem cells

      MOLECULAR AND CELLULAR BIOLOGY
    34. Carlone, DL; Skalnik, DG
      CpG binding protein is crucial for early embryonic development

      MOLECULAR AND CELLULAR BIOLOGY
    35. Tefferi, A; Murphy, S
      Current opinion in essential thrombocythemia: pathogenesis, diagnosis, andmanagement

      BLOOD REVIEWS
    36. Yamane, A; Karasawa, M; Maeharal, T; Tsukamoto, N; Nojima, Y
      X chromosome methylation-based chimerism assay for sex-mismatched hematopoietic stem cell transplantation

      BONE MARROW TRANSPLANTATION
    37. Monk, M
      Of microbes, mice and man

      INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
    38. Shastry, BS
      Molecular genetics of Rett syndrome

      NEUROCHEMISTRY INTERNATIONAL
    39. Uehara, S; Hanew, K; Harada, N; Yamamori, S; Nata, M; Niikawa, N; Okamura, K
      Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature

      AMERICAN JOURNAL OF MEDICAL GENETICS
    40. Rivero, MB; Olicio, R; Lima, CR; Bonvicino, CR; Moreira, MAM; Llerena, JC; Seuanez, HN
      Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrierof an HPRT1 mutation responsible for Lesch-Nyhan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    41. Cheng, L; Gu, RA; Eble, JN; Bostwick, DG; Younger, C; MacLennan, GT; Abdul-Karim, FW; Geary, WA; Koch, MO; Zhang, SB; Ulbright, TM
      Molecular genetic evidence for different clonal origin of components of human renal angiomyolipomas

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    42. Jordan, JH; Fritsche-Polanz, R; Sperr, WR; Mitterbauer, G; Fodinger, M; Schernthaner, GH; Bankl, HC; Gebhart, W; Chott, A; Lechner, K; Valent, P
      A case of 'smouldering' mastocytosis with high mast cell burden, monoclonal myeloid cells, and C-KIT mutation Asp-816-Val

      LEUKEMIA RESEARCH
    43. Tefferi, A
      Recent progress in the pathogenesis and management of essential thrombocythemia

      LEUKEMIA RESEARCH
    44. Whybra, C; Kampmann, C; Willers, I; Davies, J; Winchester, B; Kriegsmann, J; Bruhl, K; Gal, A; Bunge, S; Beck, M
      Anderson-Fabry disease: Clinical manifestations of disease in female heterozygotes

      JOURNAL OF INHERITED METABOLIC DISEASE
    45. Kochhar, HPS; Peippo, J; King, WA
      Sex related embryo development

      THERIOGENOLOGY
    46. Lamb, DJ; Weigel, NL; Marcelli, M
      Androgen receptors and their biology

      VITAMINS AND HORMONES - ADVANCES IN RESEARCH AND APPLICATIONS, VOL 62
    47. Diaz-Cano, SJ; De Miguel, M; Blanes, A; Galera, H; Wolfe, HJ
      Contribution of the microvessel network to the clonal and kinetic profilesof adrenal cortical proliferative lesions

      HUMAN PATHOLOGY
    48. Auranen, M; Vanhala, R; Vosman, M; Levander, M; Varilo, T; Hietala, M; Riikonen, R; Peltonen, L; Jarvela, I
      MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features

      NEUROLOGY
    49. Hoffbuhr, K; Devaney, JM; LaFleur, B; Sirianni, N; Scacheri, C; Giron, J; Schuette, J; Innis, J; Marino, M; Philippart, M; Narayanan, V; Umansky, R; Kronn, D; Hoffman, EP; Naidu, S
      MeCP2 mutations in children with and without the phenotype of Rett syndrome

      NEUROLOGY
    50. Surani, MA
      Reprogramming of genome function through epigenetic inheritance

      NATURE
    51. Heim, S; Teixeira, MAR; Pandis, N
      Are some breast carcinomas polyclonal in origin?

      JOURNAL OF PATHOLOGY
    52. Diallo, R; Schaefer, KL; Poremba, C; Shivazi, N; Willmann, V; Buerger, H; Dockhorn-Dworniczak, B; Boecker, W
      Monoclonality in normal epithelium and in hyperplastic and neoplastic lesions of the breast

      JOURNAL OF PATHOLOGY
    53. Villard, L; Levy, N; Xiang, FQ; Kpebe, A; Labelle, V; Chevillard, C; Zhang, ZP; Schwartz, CE; Tardieu, M; Chelly, J; Anvret, M; Fontes, M
      Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications forthe disease

      JOURNAL OF MEDICAL GENETICS
    54. Costello, JF; Plass, C
      Methylation matters

      JOURNAL OF MEDICAL GENETICS
    55. Asplund, A; Guo, ZM; Hu, XR; Wassberg, C; Ponten, F
      Mosaic pattern of maternal and paternal keratinocyte clones in normal human epidermis revealed by analysis of X-chromosome inactivation

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    56. Nakamura, H; Hirota, S; Adachi, S; Ozaki, K; Asada, H; Kitamura, Y
      Clonal nature of seborrheic keratosis demonstrated by using the polymorphism of the human androgen receptor locus as a marker

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    57. Boye, E; Yu, Y; Paranya, G; Mulliken, JB; Olsen, BR; Bischoff, J
      Clonality and altered behavior of endothelial cells from hemangiomas

      JOURNAL OF CLINICAL INVESTIGATION
    58. Diaz-Cano, SJ; de Miguel, M; Blanes, A; Tashjian, R; Wolfe, HJ
      Germline RET 634 mutation positive MEN 2A-related C-cell hyperplasias havegenetic features consistent with intraepithelial neoplasia

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    59. Chadwick, BP; Willard, HF
      A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome

      JOURNAL OF CELL BIOLOGY
    60. Burritt, JB; DeLeo, FR; McDonald, CL; Prigge, JR; Dinauer, MC; Nakamura, M; Nauseef, WM; Jesaitis, AJ
      Phage display epitope mapping of human neutrophil flavocytochrome b(558) -Identification of two juxtaposed extracellular domains

      JOURNAL OF BIOLOGICAL CHEMISTRY
    61. Chen, CC; Fang, M; Majumder, A; Wu, HY
      A 72-base pair AT-rich DNA sequence element functions as a bacterial gene silencer

      JOURNAL OF BIOLOGICAL CHEMISTRY
    62. Lucarelli, M; Fuso, A; Strom, R; Scarpa, S
      The dynamics of myogenin site-specific demethylation is strongly correlated with its expression and with muscle differentiation

      JOURNAL OF BIOLOGICAL CHEMISTRY
    63. Lebrun, E; Revardel, E; Boscheron, C; Li, R; Gilson, E; Fourel, G
      Protosilencers in Saccharomyces cerevisiae subtelomeric regions

      GENETICS
    64. Uehara, S; Hashiyada, M; Sato, K; Sato, Y; Fujimori, K; Okamura, K
      Preferential X-chromosome inactivation in women with idiopathic recurrent pregnancy loss

      FERTILITY AND STERILITY
    65. Mermoud, JE; Tassin, AM; Pehrson, JR; Brockdorff, N
      Centrosomal association of histone macroH2A1.2 in embryonic stem cells andsomatic cells

      EXPERIMENTAL CELL RESEARCH
    66. Nesterova, TB; Barton, SC; Surani, MA; Brockdorff, N
      Loss of Xist imprinting in diploid parthenogenetic preimplantation embryos

      DEVELOPMENTAL BIOLOGY
    67. Izawa, T; Obara, T; Tanno, S; Mizukami, Y; Yanagawa, N; Kohgo, Y
      Clonality and field cancerization in intraductal papillary-mutinous tumorsof the pancreas

      CANCER
    68. Lanasa, MC; Hogge, WA; Kubik, CJ; Ness, RB; Harger, J; Nagel, T; Prosen, T; Markovic, N; Hoffman, EP
      A novel X chromosome-linked genetic cause of recurrent spontaneous abortion

      AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY
    69. Niida, Y; Stemmer-Rachamimov, AO; Logrip, M; Tapon, D; Perez, R; Kwiatkowski, DJ; Sims, K; MacCollin, M; Louis, DN; Ramesh, V
      Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomassuggests different genetic mechanisms for pathogenesis of TSC lesions

      AMERICAN JOURNAL OF HUMAN GENETICS
    70. Robertson, SP; Walsh, S; Oldridge, M; Gunn, T; Becroft, D; Wilkie, AOM
      Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: Evidence for allelism with OPD1

      AMERICAN JOURNAL OF HUMAN GENETICS
    71. Trappe, R; Laccone, F; Cobilanschi, J; Meins, M; Huppke, P; Hanefeld, F; Engel, W
      MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

      AMERICAN JOURNAL OF HUMAN GENETICS
    72. Gu, J; Roth, LM; Younger, C; Michael, H; Abdul-Karim, FW; Zhang, SB; Ulbright, TM; Eble, JN; Cheng, L
      Molecular evidence for the independent origin of extra-ovarian papillary serous tumors of low malignant potential

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    73. Lanasa, MC; Hogge, WA
      X chromosome defects as an etiology of recurrent spontaneous abortion

      SEMINARS IN REPRODUCTIVE MEDICINE
    74. Wentworth, AL; Wentworth, BC
      The avian primordial germ cell ... - An enigma of germline evolution, development and immortality

      AVIAN AND POULTRY BIOLOGY REVIEWS
    75. Uehara, S; Tamura, M; Nata, M; Ji, GJ; Yaegashi, N; Okamura, K; Yajima, A
      X-chromosome inactivation in the human trophoblast of early pregnancy

      JOURNAL OF HUMAN GENETICS
    76. Ochiai, T; Urata, Y; Yamano, T; Sonoyama, T; Yamagishi, H; Ashihara, T
      A long-term survival case of multiple hepatocellular carcinoma with metachronous lymph node metastasis

      HEPATOLOGY RESEARCH
    77. Holding, C; Bolton, V; Monk, M
      Detection of human novel developmental genes in cDNA derived from replicate individual preimplantation embryos

      MOLECULAR HUMAN REPRODUCTION
    78. De Gregorio, L; Nyhan, WL; Serafin, E; Chamoles, NA
      An unexpected affected female patient in a classical Lesch-Nyhan family

      MOLECULAR GENETICS AND METABOLISM
    79. Vrana, PB; Fossella, JA; Matteson, P; del Rio, T; O'Neill, MJ; Tilghman, SM
      Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus

      NATURE GENETICS
    80. Man, YG; Martinez, A; Avis, IM; Hong, SH; Cuttitta, F; Venzon, DJ; Mulshine, JL
      Phenotypically different cells with heterogeneous nuclear ribonucleoprotein A2/B1 overexpression show similar genetic alterations

      AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
    81. Bunting, KD; Lu, TH; Kelly, PF; Sorrentino, BP
      Self-selection by genetically modified committed lymphocyte precursors reverses the phenotype of JAK3-deficient mice without myeloablation

      HUMAN GENE THERAPY
    82. Huppke, P; Laccone, F; Kramer, N; Engel, W; Hanefeld, F
      Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients

      HUMAN MOLECULAR GENETICS
    83. Hansen, RS; Stoger, R; Wijmenga, C; Stanek, AM; Canfield, TK; Luo, P; Matarazzo, MR; D'Esposito, M; Feil, R; Gimelli, G; Weemaes, CMR; Laird, CD; Gartler, SM
      Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant

      HUMAN MOLECULAR GENETICS
    84. Grunau, C; Hindermann, W; Rosenthal, A
      Large-scale methylation analysis of human genomic DNA reveals tissue-specific differences between the methylation profiles of genes and pseudogenes

      HUMAN MOLECULAR GENETICS
    85. Meller, VH
      Dosage compensation: making 1X equal 2X

      TRENDS IN CELL BIOLOGY
    86. Garcia, SB; Novelli, M; Wright, NA
      The clonal origin and clonal evolution of epithelial tumours

      INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY
    87. Van den Veyver, IB; Zoghbi, HY
      Methyl-CpG-binding protein 2 mutations in Rett syndrome

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    88. Okamoto, I; Tan, SS; Takagi, N
      X-chromosome inactivation in XX androgenetic mouse embryos surviving implantation

      DEVELOPMENT
    89. Tada, T; Obata, Y; Tada, M; Goto, Y; Nakatsuji, N; Tan, SS; Kono, T; Takagi, N
      Imprint switching for non-random X-chromosome inactivation during mouse oocyte growth

      DEVELOPMENT
    90. Costanzi, C; Stein, P; Worrad, DM; Schultz, RM; Pehrson, JR
      Histone macroH2A1 is concentrated in the inactive X chromosome of female preimplantation mouse embryos

      DEVELOPMENT
    91. Romer, JT; Ashworth, A
      The upstream region of the mouse Xist gene contains two ribosomal protein pseudogenes

      MAMMALIAN GENOME
    92. Hong, YK; Ontiveros, SD; Strauss, WM
      A revision of the human XIST gene organization and structural comparison with mouse Xist

      MAMMALIAN GENOME
    93. Guo, ZM; Ponten, F; Wilander, E; Ponten, J
      Clonality of precursors of cervical cancer and their genetical links to invasive cancer

      MODERN PATHOLOGY
    94. Cheng, TH; Gartenberg, MR
      Yeast heterochromatin is a dynamic structure that requires silencers continuously

      GENES & DEVELOPMENT
    95. Fischer, A
      T-lymphocyte immunodeficiencies - Novel phenotypes

      IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA
    96. Hol, FA; Schepens, MT; van Beersum, SEC; Redolfi, E; Affer, M; Vezzoni, P; Hamel, BCJ; Karnes, PS; Mariman, ECM; Zucchi, I
      Identification and characterization of an Xq26-q27 duplication in a familywith spina bifida and panhypopituitarism suggests the involvement of two distinct genes

      GENOMICS
    97. Reizis, B; Lee, JT; Leder, P
      Homologous genomic fragments in the mouse pre-T cell receptor alpha (pTa) and Xist loci

      GENOMICS
    98. Uchida, T; Ohashi, H; Aoki, E; Nakahara, Y; Hotta, T; Murate, T; Saito, H; Kinoshita, T
      Clonality analysis by methylation-specific PCR for the human androgen-receptor gene (HUMARA-MSP)

      LEUKEMIA
    99. Miedlich, S; Krohn, K; Lamesch, P; Muller, A; Paschke, R
      Frequency of somatic MEN1 gene mutations in monoclonal parathyroid tumoursof patients with primary hyperparathyroidism

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    100. Gregg, XT; Kralovics, R; Prchal, JT
      A polymorphism of the X-linked gene IDS increases the number of females informative for transcriptional clonality assays

      AMERICAN JOURNAL OF HEMATOLOGY


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Documento generato il 25/01/21 alle ore 12:45:08