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La ricerca find articoli where soggetti phrase all words 'CHROMOSOME-17' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 581 riferimenti
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    1. Hutton, M; Lewis, J; Dickson, D; Yen, SH; McGowan, E
      Analysis of tauopathies with transgenic mice

      TRENDS IN MOLECULAR MEDICINE
    2. Kowalska, A; Asada, T; Arima, K; Kumakiri, C; Kozubski, W; Takahashi, K; Tabira, T
      Genetic analysis in patients with familial and sporadic frontotemporal dementia: Two tau mutations in only familial cases and no association with apolipoprotein epsilon 4

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    3. Herrington, CS; Worsham, M; Southern, SA; Mackowiak, P; Wolman, SR
      Loss of sequences on the short arm of chromosome 17 is a late event in squamous carcinoma of the cervix

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    4. Matsumoto, Y; Ishiko, O; Deguchi, M; Nakagawa, E; Ogita, S
      Cyclooxygenase-2 expression in normal ovaries and epithelial ovarian neoplasms

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    5. Terada, R; Yasutake, T; Nakamura, S; Hisamatsu, T; Nakagoe, T; Ayabe, H; Tagawa, Y
      Evaluation of metastatic potential of gastric tumors by staining for proliferating cell nuclear antigen and chromosome 17 numerical aberrations

      ANNALS OF SURGICAL ONCOLOGY
    6. Drut, R; Drut, RM; Ortolani, C
      Metastatic metanephric adenoma with foci of papillary carcinoma in a child- A combined histologic, immunohistochemical, and FISH study

      INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY
    7. Van Roy, N; Van Limbergen, H; Vandesompele, J; Van Gele, M; Poppe, B; Salwen, H; Laureys, G; Manoel, N; De Paepe, A; Speleman, F
      Combined M-FISH and CGH analysis allows comprehensive description of genetic alterations in neuroblastoma cell lines

      GENES CHROMOSOMES & CANCER
    8. Wang, G; Zhao, Y; Liu, XM; Wang, L; Wu, CG; Zhang, WL; Liu, WQ; Zhang, PP; Cong, WM; Zhu, YR; Zhang, LS; Chen, SJ; Wan, DF; Zhao, XT; Haung, W; Gu, JR
      Allelic loss and gain, but not genomic instability, as the major somatic mutation in primary hepatocellular carcinoma

      GENES CHROMOSOMES & CANCER
    9. Kohno, A; Tsuzuki, S; Kasai, M; Miyamura, K; Emi, N; Tanimoto, M; Saito, H
      Acute promyelocytic leukemia with apparently normal karyotype: Molecular findings and response to all-trans retinoic acid

      LEUKEMIA & LYMPHOMA
    10. Matsumoto, Y; Ishiko, O; Sumi, T; Yoshida, H; Deguchi, M; Nakagawa, E; Haba, T; Wakasa, K; Ogita, S; Ando, Y
      Cyclooxygenase-2 expression in malignant mesenchymal tumors and related uterine lesions

      ONCOLOGY REPORTS
    11. Gotte, K; Riedel, F; Neubauer, J; Schafer, C; Coy, JF; Hormann, K
      The relationship between allelic imbalance on 17p, p53 mutation and p53 overexpression in head and neck cancer

      INTERNATIONAL JOURNAL OF ONCOLOGY
    12. Van der Looij, M; Papp, J; Sztan, M; Pulay, T; Elfadil, I; Besznyak, I; Toth, J; Devilee, P; Olah, E
      Allelic imbalance and microsatellite instability in BRCA1 associated breast and ovarian tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    13. Huang, SW; Ardlie, KG; Yu, HT
      Frequency and distribution of t-haplotypes in the Southeast Asian house mouse (Mus musculus castaneus) in Taiwan

      MOLECULAR ECOLOGY
    14. Garcia, ML; Cleveland, DV
      Going new places using an old MAP: tau, microtubules and human neurodegenerative disease

      CURRENT OPINION IN CELL BIOLOGY
    15. Zwart, R; Verhaagh, S; de Jong, J; Lyon, M; Barlow, DP
      Genetic analysis of the organic cation transporter genes Orct2/Slc22a2 andOrct3/Slc22a3 reduces the critical region for the t haplotype mutant t(w73) to 200 kb

      MAMMALIAN GENOME
    16. Kim, J; Yook, JI; Lee, EH; Ryu, MH; Yoon, JH; Hong, JC; Kim, DJ; Kim, HS
      Evaluation of premalignant potential in oral lichen planus using interphase cytogenetics

      JOURNAL OF ORAL PATHOLOGY & MEDICINE
    17. Mendez, MF; Lipton, A
      Emergent neuroleptic hypersensitivity as a herald of presenile dementia

      JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
    18. Davisson, MT; Bechtel, LJ; Akeson, EC; Fortna, A; Slavov, D; Gardiner, K
      Evolutionary breakpoints on human chromosome 21

      GENOMICS
    19. Tufarelli, C; Frischauf, AM; Hardison, R; Flint, J; Higgs, DR
      Characterization of a widely expressed gene (LUC7-LIKE; LUC7L) defining the centromeric boundary of the human alpha-globin domain

      GENOMICS
    20. Dugas, JC; Ngai, J
      Analysis and characterization of an odorant receptor gene cluster in the zebrafish genome

      GENOMICS
    21. Weinstein, MH; Dal Cin, P
      Genetics of epithelial tumors of the renal parenchyma in adults and renal cell carcinoma in children

      ANALYTICAL AND QUANTITATIVE CYTOLOGY AND HISTOLOGY
    22. Sawai, T; Nanashima, A; Tsuji, T; Yamaguchi, H; Yasutake, T; Nakagoe, T; Ayabe, H; Tagawa, Y
      Instability of chromosome 17 and the p53 locus in non-familial colorectal cancer with multiple primary malignancies

      JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH
    23. Fukushi, Y; Sato, S; Yokoyama, Y; Kudo, K; Maruyama, H; Saito, Y
      Detection of numerical aberration in chromosome 17 and c-erbB2 gene amplification in epithelial ovarian cancer using recently established dual color FISH

      EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY
    24. Boabang, P; Kurbacher, CM; Waida, A; Amo-Takyi, BK
      Detection of aberrations of chromosome 17 and p53 gene expression and their correlation to histologic grading and prognosis in primary invasive squamous cell carcinoma of the cervix

      GYNECOLOGIC AND OBSTETRIC INVESTIGATION
    25. Marchenko, GN; Strongin, AY
      MMP-28, a new human matrix metalloproteinase with an unusual cysteine-switch sequence is widely expressed in tumors

      GENE
    26. Geschwind, DH; Robidoux, J; Alarcon, M; Miller, BL; Wilhelmsen, KC; Cummings, JL; Nasreddine, ZS
      Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia

      ANNALS OF NEUROLOGY
    27. Neumann, M; Schulz-Schaeffer, W; Crowther, RA; Smith, MJ; Spillantini, MG; Goedert, M; Kretzschmar, HA
      Pick's disease associated with the novel Tau gene mutation K369I

      ANNALS OF NEUROLOGY
    28. Bird, TD; Schellenberg, GD
      The case of the missing tau, or, why didn't the mRNA bark?

      ANNALS OF NEUROLOGY
    29. Zhukareva, V; Vogelsberg-Ragaglia, V; Van Deerlin, VMD; Bruce, J; Shuck, T; Grossman, M; Clark, CM; Arnold, SE; Masliah, E; Galasko, D; Trojanowski, JQ; Lee, VMY
      Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia

      ANNALS OF NEUROLOGY
    30. Nagiec, EE; Sampson, KE; Abraham, I
      Mutated tau binds less avidly to microtubules than wildtype tau in living cells

      JOURNAL OF NEUROSCIENCE RESEARCH
    31. de Silva, R; Weiler, M; Morris, HR; Martin, ER; Wood, NW; Lees, AJ
      Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

      NEUROSCIENCE LETTERS
    32. Mann, DMA; McDonagh, AM; Pickering-Brown, SM; Kowa, H; Iwatsubo, T
      Amyloid beta protein deposition in patients with frontotemporal lobar degeneration: relationship to age and apolipoprotein E genotype

      NEUROSCIENCE LETTERS
    33. Russ, C; Lovestone, S; Baker, M; Pickering-Brown, SM; Andersen, PM; Furlong, R; Mann, D; Powell, JF
      The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease

      NEUROSCIENCE LETTERS
    34. Tajiri, T; Tanaka, S; Shono, K; Kinoshita, Y; Fujii, Y; Suita, S; Ihara, K; Hara, T
      Quick quantitative analysis of gene dosages associated with prognosis in neuroblastoma

      CANCER LETTERS
    35. Tolnay, M; Probst, A
      Frontotemporal lobar degeneration - An update on clinical, pathological and genetic findings

      GERONTOLOGY
    36. Disse-Nicodeme, S; Desitter, I; Fiquet-Kempf, B; Houot, AM; Stern, N; Delahousse, M; Potier, J; Ader, JL; Jeunemaitre, X
      Genetic heterogeneity of familial hyperkalaemic hypertension

      JOURNAL OF HYPERTENSION
    37. Querzoli, P; Albonico, G; de Iasio, MG; Ferretti, S; Rinaldi, R; Cariello, A; Pedriali, M; Matteuzzi, M; Maestri, I; Nenci, I
      Biophenotypes and survival of BRCA1 and TP53 deleted breast cancer in young women

      BREAST CANCER RESEARCH AND TREATMENT
    38. Portwine, C; Chilton-MacNeill, S; Brown, C; Sexsmith, E; McLaughlin, J; Malkin, D
      Absence of germline and somatic p53 alterations in children with sporadic brain tumors

      JOURNAL OF NEURO-ONCOLOGY
    39. Mavrogiannis, LA; Argyrokastritis, A; Tzitzikas, N; Dermitzakis, E; Sarafidou, T; Patsalis, PC; Moschonas, NK
      ZNF232: structure and expression analysis of a novel human C2H2 zinc finger gene(1), member of the SCAN/LeR domain subfamily

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    40. Liu, SH; Li, Q; Pang, WX; Bo, LJ; Qin, S; Liu, XP; Teng, QL; Qian, LS; Wang, JX
      A new complex variant t(4;15;17) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation and literature review

      CANCER GENETICS AND CYTOGENETICS
    41. Hoff, C; Mollenhauer, J; Waldau, B; Hamann, U; Poustka, A
      Allelic imbalance and fine mapping of the 17p13.3 subregion in sporadic breast carcinomas

      CANCER GENETICS AND CYTOGENETICS
    42. Muir, TE; Cheville, JC; Lager, DJ
      Metanephric adenoma, nephrogenic rests, and Wilms' tumor - A histologic and immunophenotypic comparison

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    43. Vandesompele, J; Speleman, F; Van Roy, N; Laureys, C; Brinkschmidt, C; Christiansen, H; Lampert, F; Lastowska, M; Bown, N; Pearson, A; Nicholson, JC; Ross, F; Combaret, V; Delattre, O; Feuerstein, BC; Plantaz, D
      Multicentre analysis of patterns of DNA gains and losses in 204 neuroblastoma tumors: How many genetic subgroups are there?

      MEDICAL AND PEDIATRIC ONCOLOGY
    44. Houlden, H; Baker, M; Morris, HR; MacDonald, N; Pickering-Brown, S; Adamson, J; Lees, AJ; Rossor, MN; Quinn, NP; Kertesz, A; Khan, MN; Hardy, J; Lantos, PL; George-Hyslop, PS; Munoz, DG; Mann, D; Lang, AE; Bergeron, C; Bigio, EH; Litvan, I; Bhatia, KP; Dickson, D; Wood, NW; Hutton, M
      Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

      NEUROLOGY
    45. Hutton, M
      Missense and splice site mutations in tau associated with FTDP-17: Multiple pathogenic mechanisms

      NEUROLOGY
    46. Lee, VMY; Trojanowski, JQ
      Transgenic mouse models of tauopathies: Prospects for animal models of Pick's disease

      NEUROLOGY
    47. Watanabe, T; Oda, Y; Tamiya, S; Masuda, K; Tsuneyoshi, M
      Malignant peripheral nerve sheath tumour arising within neurofibroma. An immunohistochemical analysis in the comparison between benign and malignant components

      JOURNAL OF CLINICAL PATHOLOGY
    48. Alpy, F; Stoeckel, ME; Dierich, A; Escola, JM; Wendling, C; Chenard, MP; Vanier, MT; Gruenberg, J; Tomasetto, C; Rio, MC
      The steroidogenic acute regulatory protein homolog MLN64, a late endosomalcholesterol-binding protein

      JOURNAL OF BIOLOGICAL CHEMISTRY
    49. Connell, JW; Gibb, GM; Betts, JC; Blackstock, WP; Gallo, JM; Lovestone, S; Hutton, M; Anderton, BH
      Effects of FTDP-17 mutations on the in vitro phosphorylation of tau by glycogen synthase kinase 3 beta identified by mass spectrometry demonstrate certain mutations exert long-range conformational changes

      FEBS LETTERS
    50. Fabre, SF; Forsell, C; Viitanen, M; Sjogren, M; Wallin, A; Blennow, K; Blomberg, M; Andersen, C; Wahlund, LO; Lannfelt, L
      Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon 4 frequency, but no tau genemutations

      EXPERIMENTAL NEUROLOGY
    51. Kauraniemi, P; Barlund, M; Monni, O; Kallioniemi, A
      New amplified and highly expressed genes discovered in the ERBB2 amplicon in breast cancer by cDNA microarrays

      CANCER RESEARCH
    52. Gilbertson, R; Wickramasinghe, C; Hernan, R; Balaji, V; Hunt, D; Jones-Wallace, D; Crolla, J; Perry, R; Lunec, J; Pearson, A; Ellison, D
      Clinical and molecular stratification of disease risk in medulloblastoma

      BRITISH JOURNAL OF CANCER
    53. Anderson, J; Kempski, H; Hill, L; Rampling, D; Gordon, T; Michalski, A
      Neuroblastoma in monozygotic twins - a case of probable twin-to-twin metastasis

      BRITISH JOURNAL OF CANCER
    54. El-Shazly, SD; Seo, KW; El-Nahas, A; Ables, GP; Asano, A; Watanabe, T
      Male hybrid sterility of mice with the genomic region of the Kit(W) mutation and the Kit(S) allele from Mus spretus

      BIOCHEMICAL GENETICS
    55. Vandeputte, DAA; Meije, CB; van Dartel, M; Leenstra, S; IJlst-Keizers, H; Das, PK; Troost, D; Bosch, DA; Baas, F; Hulsebos, TJM
      GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytoma

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    56. Miller, BL
      Tan mutations - Center tent or sideshow?

      ARCHIVES OF NEUROLOGY
    57. Poorkaj, P; Grossman, M; Steinbart, E; Payami, H; Sadovnick, A; Nochlin, D; Tabira, T; Trojanowski, JQ; Borson, S; Galasko, D; Reich, S; Quinn, B; Schellenberg, G; Bird, TD
      Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia

      ARCHIVES OF NEUROLOGY
    58. Morris, HR; Khan, MN; Janssen, JC; Brown, JM; Perez-Tur, J; Baker, M; Ozansoy, M; Hardy, J; Hutton, M; Wood, NW; Lees, AJ; Revesz, T; Lantos, P; Rossor, MN
      The genetic and pathological classification of familial frontotemporal dementia

      ARCHIVES OF NEUROLOGY
    59. Poorkaj, P; Tsuang, D; Wijsman, E; Steinbart, E; Garruto, RM; Craig, UK; Chapman, NH; Anderson, L; Bird, TD; Plato, CC; Perl, DP; Weiderholt, W; Galasko, D; Schellenberg, GD
      TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonismdementia complex of Guam

      ARCHIVES OF NEUROLOGY
    60. Stockton, DW; Meade, RA; Netscher, DT; Epstein, MJ; Shenaq, SM; Shaffer, LG; Lupski, JR
      Hereditary neuropathy with liability to pressure palsies is not a major cause of idiopathic carpal tunnel syndrome

      ARCHIVES OF NEUROLOGY
    61. Perry, A; Roth, KA; Banerjee, R; Fuller, CE; Gutmann, DH
      NF1 deletions in S-100 protein-positive and negative cells of sporadic andneurofibromatosis 1 (NF1)-associated plexiform neurofibromas and malignantperipheral nerve sheath tumors

      AMERICAN JOURNAL OF PATHOLOGY
    62. D'Souza, I; Schellenberg, GD
      Regulation of four-repeat tau expression: Interactions between exon and intron splicing regulatory sequences

      ALZHEIMER'S DISEASE
    63. Xu, XW; Acs, G; Yu, GH; Guttenberg, M; Vautour, RJ
      Aspiration cytology of metanephric adenoma of the kidney

      DIAGNOSTIC CYTOPATHOLOGY
    64. Wang, J; Morimitsu, Y; Okamoto, S; Hisaoka, M; Ishida, T; Sheng, WQ; Hashimoto, H
      COL1A1-PDGFB fusion transcripts in fibrosarcomatous areas of six dermatofibrosarcomas protuberans

      JOURNAL OF MOLECULAR DIAGNOSTICS
    65. Gilad, Y; Segre, D; Skorecki, K; Nachman, MW; Lancet, D; Sharon, D
      Dichotomy of single-nucleotide polymorphism haplotypes in olfactory receptor genes and pseudogenes

      NATURE GENETICS
    66. Messiaen, LM; Callens, T; Mortier, G; Beysen, D; Vandenbroucke, I; Van Roy, N; Speleman, F; De Paepe, A
      Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects

      HUMAN MUTATION
    67. Wallace, MR; Rasmussen, SA; Lim, IT; Gray, BA; Zori, RT; Muir, D
      Culture of cytogenetically abnormal Schwann cells from benign and malignant NFI tumors

      GENES CHROMOSOMES & CANCER
    68. Safronova, LD; Shustrova, IV; Ryskov, AP
      Structural organization and evolution of the t complex in the genus Mus

      RUSSIAN JOURNAL OF GENETICS
    69. Onchi, H; Hirose, K; Yamaguchi, A; Noriki, S; Fukuda, M
      Prognostic value of numerical aberrations of chromosome 17 in differentiated gastric cancer: Evaluation by multivariate regression analysis

      ONCOLOGY REPORTS
    70. Thomas, DG; Jacques, SM; Flore, LA; Feldman, B; Evans, MI; Qureshi, F
      Prenatal diagnosis of Smith-Magenis syndrome (del 17p11.2)

      FETAL DIAGNOSIS AND THERAPY
    71. Berciano, J; Garcia, A; Calleja, J; Combarros, O
      Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication

      NEUROMUSCULAR DISORDERS
    72. Knight, J; Gardner, GTB; Clark, AJL; Caulfield, MJ
      Investigation of chromosome 17q as a locus for human essential hypertension in African Caribbeans

      JOURNAL OF HUMAN HYPERTENSION
    73. Islam, A; Kageyama, H; Takada, N; Kawamato, T; Takayasu, H; Isogai, E; Ohira, M; Hashizume, K; Kobayashi, H; Kaneko, Y; Nakagawara, A
      High expression of Survivin, mapped to 17q25, is significantly associated with poor prognostic factors and promotes cell survival in human neuroblastoma

      ONCOGENE
    74. Hatt, H
      Follow your nose: Mechanisms of signal transduction

      ZOOLOGY-ANALYSIS OF COMPLEX SYSTEMS
    75. Watatani, M; Inui, H; Nagayama, K; Imanishi, Y; Nishimura, K; Hashimoto, Y; Yamauchi, E; Hojo, T; Kotsuma, Y; Yamato, M; Matsunami, N; Yasutomi, M
      Identification of high-risk breast cancer patients from genetic changes oftheir tumors

      SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY
    76. Fossella, J; Samant, SA; Silver, LM; King, SM; Vaughan, KT; Olds-Clarke, P; Johnson, KA; Mikami, A; Vallee, RB; Pilder, SH
      An axonemal dynein at the Hybrid Sterility 6 locus: implications for t haplotype-specific male sterility and the evolution of species barriers

      MAMMALIAN GENOME
    77. Goedert, M; Spillantini, MG
      Tau mutations in frontotemporal dementia FTDP-17 and their relevance for Alzheimer's disease

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    78. Forman, MS; Lee, VMY; Trojanowski, JQ
      New insights into genetic and molecular mechanisms of brain degeneration in tauopathies

      JOURNAL OF CHEMICAL NEUROANATOMY
    79. Hoff, C; Seranski, P; Mollenhauer, J; Korn, B; Detzel, T; Reinhardt, R; Ramser, J; Poustka, A
      Physical and transcriptional mapping of the 17p13.3 region that is frequently deleted in human cancer

      GENOMICS
    80. van Slegtenhorst, M; Lewis, J; Hutton, M
      The molecular genetics of the tauopathies

      EXPERIMENTAL GERONTOLOGY
    81. Kudo, K; Sato, S; Yokoyama, Y; Fukushi, Y; Maruyama, H; Saito, Y
      Clinical significance of numerical aberrations on chromosome 17 in uterinecervical and endometrial neoplasias

      EUROPEAN JOURNAL OF GYNAECOLOGICAL ONCOLOGY
    82. Sharon, D; Gilad, Y; Glusman, G; Khen, M; Lancet, D; Kalush, F
      Identification and characterization of coding single-nucleotide polymorphisms within a human olfactory receptor gene cluster

      GENE
    83. Ijichi, H; Tanaka, T; Nakamura, T; Yagi, H; Hakuba, A; Sato, M
      Molecular cloning and characterization of a human homologue of TBPIP, a BRCA1 locus-related gene

      GENE
    84. Lippa, CF; Zhukareva, V; Kawarai, T; Uryu, K; Shafiq, M; Nee, LE; Grafman, J; Liang, Y; St George-Hyslop, PH; Trojanowski, JQ; Lee, VMY
      Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation

      ANNALS OF NEUROLOGY
    85. Pickering-Brown, S; Baker, M; Yen, SH; Liu, WK; Hasegawa, M; Cairns, N; Lantos, PL; Rossor, M; Iwatsubo, T; Davies, Y; Allsop, D; Furlong, R; Owen, F; Hardy, J; Mann, D; Hutton, M
      Pick's disease is associated with mutations in the tau gene

      ANNALS OF NEUROLOGY
    86. Spillantini, MG; Yoshida, H; Rizzini, C; Lantos, PL; Khan, N; Rossor, MN; Goedert, M; Brown, J
      A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies

      ANNALS OF NEUROLOGY
    87. Di Maria, E; Tabaton, M; Vigo, T; Abbruzzese, G; Bellone, E; Donati, C; Frasson, E; Marchese, R; Montagna, P; Munoz, DG; Pramstaller, PP; Zanusso, G; Ajmar, F; Mandich, P
      Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

      ANNALS OF NEUROLOGY
    88. Marinho, AF; Botelho, M; Schmitt, FC
      Evaluation of numerical abnormalities of chromosomes 1 and 17 in proliferative epithelial breast lesions using fluorescence in situ hybridization

      PATHOLOGY RESEARCH AND PRACTICE
    89. Tolnay, M; Spillantini, MG; Rizzini, C; Eccles, D; Lowe, J; Ellison, D
      A new case of frontotemporal dementia and parkinsonism resulting from an intron 10+3-splice site mutation in the tau gene: clinical and pathological features

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    90. Kwon, JM; Nowotny, P; Shah, PK; Chakraverty, S; Norton, J; Morris, JC; Goate, AM
      Tau polymorphisms are not associated with Alzheimer's disease

      NEUROSCIENCE LETTERS
    91. Ando, Y; Iwase, H; Ichihara, S; Toyoshima, S; Nakamura, T; Yamashita, H; Toyama, T; Omoto, Y; Karamatsu, S; Mitsuyama, S; Fujii, Y; Kobayashi, S
      Loss of heterozygosity and microsatellite instability in ductal carcinoma in situ of the breast

      CANCER LETTERS
    92. Sigel, JE; Bergfeld, WF; Goldblum, JR
      A morphologic study of dermatofibrosarcoma protuberans: expansion of a histologic profile

      JOURNAL OF CUTANEOUS PATHOLOGY
    93. Arnold, SE; Han, LY; Clark, CM; Grossman, M; Trojanowski, JQ
      Quantitative neurohistological features of frontotemporal degeneration

      NEUROBIOLOGY OF AGING
    94. Walther, T; Voigt, JP; Fink, H; Bader, M
      Sex specific behavioural alterations in Mas-deficient mice

      BEHAVIOURAL BRAIN RESEARCH
    95. Cipollini, G; Moretti, A; Ghimenti, C; Viacava, P; Bevilacqua, G; Caligo, MA
      Mutational analysis of the NM23.H1 gene in human breast cancer

      CANCER GENETICS AND CYTOGENETICS
    96. Sonobe, H; Iwata, J; Komatsu, T; Fukushima, A; Hayashi, N; Moriki, T; Shimizu, K; Ohtsuki, Y
      A giant cell angiofibroma involving 6q

      CANCER GENETICS AND CYTOGENETICS
    97. Mynett-Johnson, L; Kealey, C; Claffey, E; Curtis, D; Bouchier-Hayes, L; Powell, C; McKeon, P
      Multimarkerhaplotypes within the serotonin transporter gene suggest evidence of an association with bipolar disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    98. Hussain, SZ; Evans, AL; Ahmed, OA; Jones, D; McDermot, KD; Svennevik, EC; Hastings, RJ
      Non-syndromic mental retardation segregating with an apparently balanced t(1;17) reciprocal translocation through three generations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    99. Avery, AK; Beckstead, J; Renshaw, AA; Corless, CL
      Use of antibodies to RCC and CD10 in the differential diagnosis of renal neoplasms

      AMERICAN JOURNAL OF SURGICAL PATHOLOGY
    100. Otis, CN; Krebs, PA; Quezado, MM; Albuquerque, A; Bryant, B; San Juan, X; Kleiner, D; Sobel, ME; Merino, MJ
      Loss of heterozygosity in P53, BRCA1, and estrogen receptor genes and correlation to expression of p53 protein in ovarian epithelial tumors of different cell types and biological behavior

      HUMAN PATHOLOGY


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Documento generato il 21/01/21 alle ore 05:49:20