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La ricerca find articoli where soggetti phrase all words 'CHROMOSOME-10' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 351 riferimenti
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    1. Macoska, JA; Xu, JL; Ziemnicka, D; Schwab, TS; Rubin, MA; Kotula, L
      Loss of expression of human spectrin src homology domain binding protein 1is associated with 10p loss in human prostatic adenocarcinoma

      NEOPLASIA
    2. Di Palma, F; Holme, RH; Bryda, EC; Belyantseva, IA; Pellegrino, R; Kachar, B; Steel, KP; Noben-Trauth, K
      Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

      NATURE GENETICS
    3. Ljubimova, JY; Khazenzon, NM; Chen, ZT; Neyman, YI; Turner, L; Riedinger, MS; Black, KL
      Gene expression abnormalities in human glial tumors identified by gene array

      INTERNATIONAL JOURNAL OF ONCOLOGY
    4. Julies, MG; Moore, SW; Kotze, MJ; du Plessis, L
      Novel RET mutations in Hirschsprung's disease patients from the diverse South African population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Chernova, OB; Hunyadi, A; Malaj, E; Pan, HQ; Crooks, C; Roe, B; Cowell, JK
      A novel member of the WD-repeat gene family, WDR11, maps to the 10q26 region and is disrupted by a chromosome translocation in human glioblastoma cells

      ONCOGENE
    6. Liu, JM; Yuan, Y; Huan, J; Shen, ZY
      Inhibition of breast and brain cancer cell growth by BCCIP alpha, an evolutionarily conserved nuclear protein that interacts with BRCA2

      ONCOGENE
    7. Deng, AY; Dutil, J; Sivo, Z
      Utilization of marker-assisted congenics to map two blood pressure quantitative trait loci in Dahl rats

      MAMMALIAN GENOME
    8. Brannan, CI; Disteche, CM; Park, LS; Copeland, NG; Jenkins, NA
      Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice

      MAMMALIAN GENOME
    9. Hino, O; Okimoto, K; Kouchi, M; Sakurai, J
      A novel renal carcinoma predisposing gene of the Nihon rat maps on chromosome 10

      JAPANESE JOURNAL OF CANCER RESEARCH
    10. Davisson, MT; Bechtel, LJ; Akeson, EC; Fortna, A; Slavov, D; Gardiner, K
      Evolutionary breakpoints on human chromosome 21

      GENOMICS
    11. Pletcher, MT; Wiltshire, T; Cabin, DE; Villanueva, M; Reeves, RH
      Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21

      GENOMICS
    12. Zheng, QY; Johnson, KR
      Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice

      HEARING RESEARCH
    13. Lernmers, RJLF; de Kievit, P; van Geel, M; van der Wielen, MJR; Bakker, E; Padberg, GW; Frants, RR; van der Maarel, SM
      Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis

      ANNALS OF NEUROLOGY
    14. Loeper, S; Romeike, BFM; Heckmann, N; Jung, V; Henn, W; Feiden, W; Zang, KD; Urbschat, S
      Frequent mitotic errors in tumor cells of genetically micro-heterogeneous glioblastomas

      CYTOGENETICS AND CELL GENETICS
    15. Taj, MM; Tawil, RJ; Engstrom, LD; Zeng, Z; Hwang, C; Sanda, MG; Wechsler, DS
      Mxil, a Myc antagonist, suppresses proliferation of DU145 human prostate cells

      PROSTATE
    16. Strefford, JC; Lillington, DM; Young, BD; Oliver, RTD
      The use of multicolor fluorescence technologies in the characterization ofprostate carcinoma cell lines: a comparison of multiplex fluorescence in situ hybridization and spectral karyotyping data

      CANCER GENETICS AND CYTOGENETICS
    17. Jain, R; Jones, C
      Hydrops fetalis in an interstitial deletion of chromosome 10

      AMERICAN JOURNAL OF MEDICAL GENETICS
    18. Tada, K; Shiraishi, S; Kamiryo, T; Nakamura, H; Hirano, H; Kuratsu, JI; Kochi, M; Saya, H; Ushio, Y
      Analysis of loss of heterozygosity on chromosome 10 in patients with malignant astrocytic tumors: correlation with patient age and survival

      JOURNAL OF NEUROSURGERY
    19. Li, FY; Nikali, K; Gregan, J; Leibiger, I; Leibiger, B; Schweyen, R; Larsson, C; Suomalainen, A
      Characterization of a novel human putative mitochondrial transporter homologous to the yeast mitochondrial RNA splicing proteins 3 and 4

      FEBS LETTERS
    20. Price, RA; Li, WD; Bernstein, A; Crystal, A; Golding, EM; Weisberg, SJ; Zuckerman, WA
      A locus affecting obesity in human chromosome region 10p12

      DIABETOLOGIA
    21. Yehia, G; Razavi, R; Memin, E; Schlotter, F; Molina, CA
      The expression of inducible cAMP early repressor (ICER) is altered in prostate cancer cells and reverses the transformed phenotype of the LNCaP prostate tumor cell line

      CANCER RESEARCH
    22. Bork, JM; Peters, LM; Riazuddin, S; Bernstein, SL; Ahmed, ZM; Ness, SL; Polomeno, R; Ramesh, A; Schloss, M; Srisailpathy, CRS; Wayne, S; Bellman, S; Desmukh, D; Ahmed, Z; Khan, SN; Kaloustian, VMD; Li, XC; Lalwani, A; Riazuddin, S; Bitner-Glindzicz, M; Nance, WE; Liu, XZ; Wistow, G; Smith, RJH; Griffith, AJ; Wilcox, ER; Friedman, TB; Morell, RJ
      Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 arecaused by allelic mutations of the novel cadherin-like gene CDH23

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. Reis, RH; Nakamura, M; Masuoka, J; Watanabe, T; Colella, S; Yonekawa, Y; Kleihues, P; Ohgaki, H
      Mutation analysis of hBUB1, hBUBR1 and hBUB3 genes in glioblastomas

      ACTA NEUROPATHOLOGICA
    24. Le, HN; Norton, JA
      Perspective on RET proto-oncogene and thyroid cancer

      CANCER JOURNAL
    25. Zhou, X; Kemp, BL; Khuri, FR; Liu, D; Lee, JJ; Wu, WG; Hong, WK; Mao, L
      Prognostic implication of microsatellite alteration profiles in early-stage non-small cell lung cancer

      CLINICAL CANCER RESEARCH
    26. Kato, H; Kato, S; Kumabe, T; Sonoda, Y; Yoshimoto, T; Kato, S; Han, SY; Suzuki, T; Shibata, H; Kanamaru, R; Ishioka, C
      Functional evaluation of p53 and PTEN gene mutations in gliomas

      CLINICAL CANCER RESEARCH
    27. Scheuba, C; Kaserer, K; Kotzmann, H; Bieglmayer, C; Niederle, B; Vierhapper, H
      Prevalence of C-cell hyperplasia in patients with normal basal and pentagastrin-stimulated calcitonin

      THYROID
    28. Cargill, SL; Medrano, JF; Famula, TR; Anderson, GB
      Effects of the high growth (HG) mutation on reproduction in high growth (HG) female mice

      GROWTH DEVELOPMENT AND AGING
    29. Lorda-Sanchez, I; Garcia-Ruiz, PJ; De Alba, MR; Montoya, J; Playan, A; Sarasa, JL; Trujillo, MJ; Sanz, R; Ramos, C; Ayuso, C
      A MELAS phenotype and a paternal inherited inversion of chromosome 10 in afemale patient

      GENETIC COUNSELING
    30. Lukusa, T; Fryns, JP
      Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence

      GENETIC COUNSELING
    31. Corvi, R; Berger, N; Balczon, R; Romeo, G
      RET/PCM-1: a novel fusion gene in papillary thyroid carcinoma

      ONCOGENE
    32. Reifenberger, J; Wolter, M; Bostrom, J; Buschges, R; Schulte, KW; Megahed, M; Ruzicka, T; Reifenberger, G
      Allelic losses on chromosome arm 10q and mutation of the PTEN (MMAC1) tumour suppressor gene in primary and metastatic malignant melanomas

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    33. Krenova, D; Jirsova, Z; Bila, V; Kasparek, R; Pravenec, M; Kren, V
      Genetics of rat hypodactyly

      JOURNAL OF EXPERIMENTAL ANIMAL SCIENCE
    34. Moore, SW; Johnson, G; Schneider, JW
      Elevated tissue immunoglobulins in Hirschsprung's disease - Indication of early immunologic response

      EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    35. Somerville, RPT; Chernova, O; Liu, SQ; Shoshan, Y; Cowell, JK
      Identification of the promoter, genomic structure, and mouse ortholog of LGI1

      MAMMALIAN GENOME
    36. Fukaya, H; Suzuki, C; Yasuta, H; Ohtani, I
      Temporal bone findings in multiple endocrine neoplasia type 2B

      EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY
    37. Majima, S; Kajino, K; Fukuda, T; Otsuka, F; Hino, O
      A novel gene "Niban" upregulated in renal carcinogenesis: Cloning by the cDNA-amplified fragment length polymorphism approach

      JAPANESE JOURNAL OF CANCER RESEARCH
    38. Liu, JH; Babaian, DC; Liebert, M; Steck, PA; Kagan, J
      Inactivation of MMAC1 in bladder transitional-cell carcinoma cell lines and specimens

      MOLECULAR CARCINOGENESIS
    39. Alagramam, KN; Zahorsky-Reeves, J; Wright, CG; Pawlowski, KS; Erway, LC; Stubbs, L; Woychik, RP
      Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

      HEARING RESEARCH
    40. Majores, M; Bagli, M; Papassotiropoulos, A; Schwab, SG; Jessen, F; Rao, ML; Maier, W; Heun, R
      Allelic association between the D10S1423 marker and Alzheimer's disease ina German population

      NEUROSCIENCE LETTERS
    41. Caterina, JJ; Shi, J; Kozak, CA; Engler, JA; Birkedal-Hansen, H
      Characterization, expression analysis and chromosomal mapping of mouse Matrix Metalloproteinase-19 (MMP-19)

      MOLECULAR BIOLOGY REPORTS
    42. Maddox, JF; Andrews, AE; Gill, CA; Bottema, CD
      Linkage and physical mapping of the sheep perforin (PRF1) gene to OAR 25

      ANIMAL GENETICS
    43. Peyrollier, K; Hajduch, E; Gray, A; Litherland, GJ; Prescott, AR; Leslie, NR; Hundal, HS
      A role for the actin cytoskeleton in the hormonal and growth-factor-mediated activation of protein kinase B

      BIOCHEMICAL JOURNAL
    44. van der Knaap, JA; van den Boom, V; Kuipers, J; van Eijk, MJT; van der Vliet, PC; Timmers, HTM
      The gene for human TATA-binding-protein-associated factor (TAF(II)) 170: structure, promoter and chromosomal localization

      BIOCHEMICAL JOURNAL
    45. Fleishman, EV; Sokova, OI; Kirichenko, OP; Konstantinova, LN; Popa, AV; Volkova, MA
      Chromosome translocation t(10;11) in acute nonlymphoblastic leukemia.

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    46. Levy, D; DeStefano, AL; Larson, MG; O'Donnell, CJ; Lifton, RP; Gavras, H; Cupples, LA; Myers, RH
      Evidence for a gene influencing blood pressure on chromosome 17 - Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the Framingham Heart Study

      HYPERTENSION
    47. Gesk, S; Siebert, R; Wacker, HH; Nurnberg, N; Harder, L; Lehmann, J; Kloppel, G; Grote, W; Stockle, M; Schlegelberger, B
      Lack of deletions of the PTEN/MMAC1 and MXI1 loci in renal cell carcinoma by interphase cytogenetics

      CANCER GENETICS AND CYTOGENETICS
    48. McCandless, SE; Schwartz, S; Morrison, S; Garlapati, K; Robin, NH
      Adult with an interstitial deletion of chromosome 10 [del(10)(q25.1q25.3)]: Overlap with Coffin-Lowry syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Munnes, M; Fanaei, S; Schmitz, B; Muiznieks, I; Holschneider, AM; Doerfler, W
      Familial form of Hirschsprung disease: Nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not inother candidate genes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Rubin, MA; Gerstein, A; Reid, K; Bostwick, DG; Cheng, L; Parsons, R; Papadopoulos, N
      10q23.3 loss of heterozygosity is higher in lymph node-positive (pT2-3,N+)versus lymph node-negative (pT2-3,NO) prostate cancer

      HUMAN PATHOLOGY
    51. Martucciello, G; Ceccherini, I; Lerone, M; Jasonni, V
      Pathogenesis of Hirschsprung's disease

      JOURNAL OF PEDIATRIC SURGERY
    52. Borrego, S; Ruiz, A; Saez, ME; Gimm, O; Gao, X; Lopez-Alonso, M; Hernandez, A; Wright, FA; Antinolo, G; Eng, C
      RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease

      JOURNAL OF MEDICAL GENETICS
    53. Nagasawa, K; Kitamura, K; Yasui, A; Nimura, Y; Ikeda, K; Hirai, M; Matsukage, A; Nakanishi, M
      Identification and characterization of human DNA polymerase beta 2, a DNA polymerase beta-related enzyme

      JOURNAL OF BIOLOGICAL CHEMISTRY
    54. Lee, DW; Zhang, KJ; Ning, ZQ; Raabe, EH; Tintner, S; Wieland, R; Wilkins, BJ; Kim, JM; Blough, RI; Arceci, RJ
      Proliferation-associated SNF2-like gene (PASG): A SNF2 family member altered in leukemia

      CANCER RESEARCH
    55. Martinez, A; Malone, M; Hoeger, P; Palmer, R; Harper, JI
      Lipoatrophic panniculitis and chromosome 10 abnormality

      BRITISH JOURNAL OF DERMATOLOGY
    56. Pulver, AE
      Search for schizophrenia susceptibility genes

      BIOLOGICAL PSYCHIATRY
    57. Ramet, M; Haataja, R; Marttila, R; Floros, J; Hallman, M
      Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population

      AMERICAN JOURNAL OF HUMAN GENETICS
    58. Rothmund, M
      From genetic screening towards surgical cancer prophylaxis

      DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT
    59. Horiguchi, H; Hirose, T; Sano, T; Nagahiro, S
      Loss of chromosome 10 in glioblastoma: Relation to proliferation and angiogenesis

      PATHOLOGY INTERNATIONAL
    60. Shim, HH; Nakamura, BN; Cantor, RM; Schimmenti, LA
      Identification of two single nucleotide polymorphisms in exon 8 of PAX2

      MOLECULAR GENETICS AND METABOLISM
    61. Blechschmidt, K; Schweiger, M; Wertz, K; Poulson, R; Christensen, HM; Rosenthal, A; Lehrach, H; Yaspo, ML
      The mouse AIRE gene: Comparative genomic sequencing, gene organization, and expression

      GENOME RESEARCH
    62. Steck, PA; Lin, H; Langford, LA; Jasser, SA; Koul, D; Yung, WKA; Pershouse, MA
      Functional and molecular analyses of 10q deletions in human gliomas

      GENES CHROMOSOMES & CANCER
    63. Mizoguchi, M; Inamura, T; Ikezaki, K; Iwaki, T; Oda, S; Maehara, Y; Oki, E; Terasaki, M; Fukui, M
      Patient survival and microsatellite instability in gliomas by high-resolution fluorescent analysis

      ONCOLOGY REPORTS
    64. Nelen, MR; Kremer, H; Konings, IBM; Schoute, F; van Essen, AJ; Koch, R; Woods, CG; Fryns, JP; Hamel, B; Hoefsloot, LH; Peeters, EAJ; Padberg, GW
      Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    65. Eichler, EE
      Repetitive conundrums of centromere structure and function

      HUMAN MOLECULAR GENETICS
    66. Mollenhauer, J; Holmskov, U; Wiemann, S; Krebs, I; Herbertz, S; Madsen, J; Kioschis, P; Coy, JF; Poustka, A
      The genomic structure of the DMBT1 gene: evidence for a region with susceptibility to genomic instability

      ONCOGENE
    67. Hwang, SY; Oh, B; Zhang, Z; Miller, W; Solter, D; Knowles, BB
      The mouse cornichon gene family

      DEVELOPMENT GENES AND EVOLUTION
    68. Barr, NI; Stewart, M; Tsatsanis, C; Fulton, R; Hu, M; Tsujimoto, H; Neil, JC
      The fit-1 common integration locus in human and mouse is closely linked toMYB

      MAMMALIAN GENOME
    69. Mendiola, M; Bello, MJ; Alonso, J; Leone, PE; Vaquero, J; Sarasa, JL; Kusak, ME; De Campos, JM; Pestana, A; Rey, JA
      Search for mutations of the hRAD54 gene in sporadic meningiomas with deletion at 1p32

      MOLECULAR CARCINOGENESIS
    70. Ettinger, DS
      NCCN practice guidelines for neuroendocrine tumors

      ONCOLOGY-NEW YORK
    71. Feakes, R; Sawcer, S; Chataway, J; Coraddu, F; Broadley, S; Gray, J; Jones, HB; Clayton, D; Goodfellow, PN; Compston, A
      Exploring the dense mapping of a region of potential linkage in complex disease: An example in multiple sclerosis

      GENETIC EPIDEMIOLOGY
    72. Huang, WH; Escribano, J; Sarfarazi, M; Coca-Prados, M
      Identification, expression and chromosome localization of a human gene encoding a novel protein with similarity to the pilB family of transcriptionalfactors (pilin) and to bacterial peptide methionine sulfoxide reductases

      GENE
    73. Al-Sarraj, ST
      Molecular genetic analysis of non-astrocytic gliomas

      HISTOPATHOLOGY
    74. Baima, J; Nicolaou, M; Schwartz, F; DeStefano, AL; Manolis, A; Gavras, I; Laffer, C; Elijovich, F; Farrer, L; Baldwin, CT; Gavras, H
      Evidence for linkage between essential hypertension and a putative locus on human chromosome 17

      HYPERTENSION
    75. Faraone, SV; Meyer, J; Matise, T; Svrakic, D; Pepple, J; Malaspina, D; Suarez, B; Hampe, C; Chan, G; Aelony, A; Friedman, JH; Kaufmann, C; Cloninger, CR; Tsuang, MT
      Suggestive linkage of chromosome 10p to schizophrenia is not due to transmission ratio distortion

      AMERICAN JOURNAL OF MEDICAL GENETICS
    76. Fujimoto, S; Yokochi, K; Morikawa, H; Nakano, M; Shibata, H; Togari, H; Wada, Y
      Recurrent cerebral infarctions and del(10)(p14p15.1) de novo in HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    77. Leonard, NJ; Harley, FL; Lin, CC
      Terminal deletion of chromosome 10q at band 26.1: Follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    78. Waggoner, DJ; Chow, CK; Dowton, SB; Watson, MS
      Partial monosomy of distal 10q: Three new cases and a review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    79. Li, FY; Tariq, M; Croxen, R; Morten, K; Squier, W; Newsom-Davis, J; Beeson, D; Larsson, C
      Mapping of autosomal dominant progressive external ophthalmoplegia to a 7-cM critical region on 10q24

      NEUROLOGY
    80. Adlakha, A; Rao, K; Adlakha, H; Perry, A; Crotty, TB; Scheithauer, BW; Ryu, JH
      Meningioma metastatic to the lung

      MAYO CLINIC PROCEEDINGS
    81. Schmidt, EE; Ichimura, K; Goike, HM; Moshref, A; Liu, L; Collins, VP
      Mutational profile of the PTEN gene in primary human astrocytic tumors andcultivated xenografts

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    82. Muller, MB; Schmidt, MC; Schmidt, O; Hayashi, Y; Rollbrocker, B; Waha, N; Fimmers, R; Volk, B; Warnke, P; Ostertag, CB; Wiestler, OD; von Deimling, A
      Molecular genetic analysis as a tool for evaluating stereotactic biopsies of glioma specimens

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    83. Borrego, S; Saez, ME; Ruiz, A; Gimm, O; Lopez-Alonso, M; Antinolo, G; Eng, C
      Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

      JOURNAL OF MEDICAL GENETICS
    84. Cook, L; Weaver, DD; Hartsfield, JK; Vance, GH
      De novo 10q22 interstitial deletion

      JOURNAL OF MEDICAL GENETICS
    85. Lauge, A; Lefebvre, C; Laurent-Puig, P; Caux, V; Gad, S; Eng, C; Longy, M; Stoppa-Lyonnet, D
      No evidence for germline PTEN mutations in families with breast and brain tumours

      INTERNATIONAL JOURNAL OF CANCER
    86. Zhou, XP; Li, YJ; Hoang-Xuan, K; Laurent-Puig, P; Mokhtari, K; Longy, M; Sanson, M; Delattre, JY; Thomas, G; Hamelin, R
      Mutational analysis of the PTEN gene in gliomas: Molecular and pathological correlations

      INTERNATIONAL JOURNAL OF CANCER
    87. Krenova, D; Jirsova, Z; Housa, D; Liska, F; Soltysova, L; Kasparek, R; Bila, V; Pravenec, M; Kren, V
      Genetic analysis of the rat hypodactylous mutation

      FOLIA BIOLOGICA
    88. Wu, WG; Kemp, BL; Proctor, ML; Gazdar, AF; Minna, JD; Hong, WK; Mao, L
      Expression of DMBT1, a candidate tumor suppressor gene, is frequently lostin lung cancer

      CANCER RESEARCH
    89. Davies, MA; Koul, D; Dhesi, H; Berman, R; McDonnell, TJ; McConkey, D; Yung, WKA; Steck, PA
      Regulation of Akt PKB activity, cellular growth, and apoptosis in prostatecarcinoma cells by MMAC PTEN

      CANCER RESEARCH
    90. Aveyard, JS; Skilleter, A; Habuchi, T; Knowles, MA
      Somatic mutation of PTEN in bladder carcinoma

      BRITISH JOURNAL OF CANCER
    91. Davies, MPA; Gibbs, FEM; Halliwell, N; Joyce, KA; Roebuck, MM; Rossi, ML; Salisbury, J; Sibson, DR; Tacconi, L; Walker, C
      Mutation in the PTEN/MMAC1 gene in archival low grade and high grade gliomas

      BRITISH JOURNAL OF CANCER
    92. Mao, X; Jones, TA; Tomlinson, I; Rowan, AJ; Fedorova, LI; Zelenin, AV; Mao, JI; Gutowski, NJ; Noble, M; Sheer, D
      Genetic aberrations in glioblastoma multiforme: translocation of chromosome 10 in an O-2A-like cell line

      BRITISH JOURNAL OF CANCER
    93. Cargill, SL; Medrano, JF; Anderson, GB
      Infertility in a line of mice with the high growth mutation is due to luteal insufficiency resulting from disruption at the hypothalamic-pituitary axis

      BIOLOGY OF REPRODUCTION
    94. Seeley, TW; Wang, L; Zhen, JY
      Phosphorylation of human MAD1 by the BUB1 kinase in vitro

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    95. SHIRAHAMA S; OGURA K; TAKAMI H; ITO K; TOHSEN T; MIYAUCHI A; NAKAMURA Y
      MUTATIONAL ANALYSIS OF THE RET PROTOONCOGENE IN 71 JAPANESE PATIENTS WITH MEDULLARY-THYROID CARCINOMA

      JOURNAL OF HUMAN GENETICS
    96. LIGON AH; PERSHOUSE MA; JASSER S; HONG YK; YUNG WKA; STECK PA
      DIFFERENTIALLY EXPRESSED GENE-PRODUCTS IN GLIOBLASTOMA CELLS SUPPRESSED FOR TUMORIGENICITY

      Journal of neurovirology
    97. HORIGUCHI H; HIROSE T; KANNUKI S; NAGAHIRO S; SANO T
      GLIOSARCOMA - AN IMMUNOHISTOCHEMICAL, ULTRASTRUCTURAL AND FLUORESCENCE IN-SITU HYBRIDIZATION STUDY

      Pathology international
    98. WANG SI; PARSONS R; ITTMANN M
      HOMOZYGOUS DELETION OF THE PTEN TUMOR-SUPPRESSOR GENE IN A SUBSET OF PROSTATE ADENOCARCINOMAS

      Clinical cancer research
    99. WANG SI; PARSONS R; ITTMANN M
      HOMOZYGOUS DELETION OF THE PTEN TUMOR-SUPPRESSOR GENE IN A SUBSET OF PROSTATE ADENOCARCINOMAS

      Clinical cancer research
    100. LIN H; BONDY NL; LANGFORD LA; HESS KR; DELCLOS GL; WU XF; CHAN WY; PERSHOUSE MA; YUNG WKA; STECK PA
      ALLELIC DELETION ANALYSES OF MMAC PTEN AND DMBT1 LOCI IN GLIOMAS - RELATIONSHIP TO PROGNOSTIC-SIGNIFICANCE/

      Clinical cancer research


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Documento generato il 20/10/20 alle ore 07:47:22