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    1. Viswanathan, M; Tsuchida, N; Shanmugam, G
      Selective deletion of p14(ARF) exon 1 beta of the INK4a locus in oral squamous cell carcinomas of Indians

      ORAL ONCOLOGY
    2. Mellick, GD; Buchanan, DD; Hattori, N; Brookes, AJ; Mizuno, Y; Le Couteur, DG; Silburn, PA
      The parkin gene S/N167 polymorphism in Australian Parkinson's disease patients and controls

      PARKINSONISM & RELATED DISORDERS
    3. Bleichert, A; Fiedler, W; Claussen, U; Ernst, G; Loncarevic, IF; Heller, A; Liehr, T; Kunert, C; Von Eggeling, F
      A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    4. Momoi, H; Okabe, H; Kamikawa, T; Satoh, S; Ikai, I; Yamamoto, M; Nakagawara, A; Shimahara, Y; Yamaoka, Y; Fukumoto, M
      Comprehensive allelotyping of human intrahepatic cholangiocarcinoma

      CLINICAL CANCER RESEARCH
    5. Gollin, SM
      Chromosomal alterations in squamous cell carcinomas of the head and neck: Window to the biology of disease

      HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    6. Hedrich, K; Kann, M; Lanthaler, AJ; Dalski, A; Eskelson, C; Landt, F; Schwinger, E; Vieregge, P; Lang, AE; Breakefield, XO; Ozelius, LJ; Pramstaller, PP; Klein, C
      The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

      HUMAN MOLECULAR GENETICS
    7. Dammann, R; Takahashi, T; Pfeifer, GP
      The CpG island of the novel tumor suppressor gene RASSF1A is intensely methylated in primary small cell lung carcinomas

      ONCOGENE
    8. Omran, H; Haffner, KN; Burth, S; Ala-Mello, S; Antignac, C; Hildebrandt, F
      Evidence for further genetic heterogeneity in nephronophthisis

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    9. Hildebrandt, F; Omram, H
      New insights: nephronophthisis-medullary cystic kidney disease

      PEDIATRIC NEPHROLOGY
    10. Poi, MJ; Yen, T; Li, J; Song, HJ; Lang, JC; Schuller, DE; Pearl, DK; Casto, BC; Tsai, MD; Weghorst, CM
      Somatic INK4a-ARF locus mutations: A significant mechanism of gene inactivation in squamous cell carcinomas of the head and neck

      MOLECULAR CARCINOGENESIS
    11. Sun, PC; Uppaluri, R; Schmidt, AP; Pashia, ME; Quant, EC; Sunwoo, JB; Gollin, SM; Scholnick, SB
      Transcript map of the 8p23 putative tumor suppressor region

      GENOMICS
    12. Yanaihara, N; Kohno, T; Takakura, S; Takei, K; Otsuka, A; Sunaga, N; Takahashi, M; Yamazaki, M; Tashiro, H; Fukuzumi, Y; Fujimori, Y; Hagiwara, K; Tanaka, T; Yokota, J
      Physical and transcriptional map of a 311-kb segment of chromosome 18q21, a candidate lung tumor suppressor locus

      GENOMICS
    13. Soenen, V; Lepelley, P; Gyan, E; Preudhomme, C; Lai, JL; Bauters, F; Fenaux, P; Quesnel, B
      Prognostic significance of p16(INK4a) immunocytochemistry in adult ALL with standard risk karyotype

      LEUKEMIA
    14. Cave, H; Avet-Loiseau, H; Devaux, I; Rondeau, G; Boutard, P; Lebrun, E; Mechinaud, F; Vilmer, E; Grandchamp, B
      Deletion of chromosomal region 13q14.3 in childhood acute lymphoblastic leukemia

      LEUKEMIA
    15. Lu, CS; Wu, JC; Tsai, CH; Chen, RS; Chou, YHW; Hattori, N; Yoshino, H; Mizuno, Y
      Clinical and genetic studies on familial parkinsonism: The first report ona parkin gene mutation in a Taiwanese family

      MOVEMENT DISORDERS
    16. Corti, O; Brice, A
      Parkin and Parkinson's: More than homonymy?

      ANNALS OF NEUROLOGY
    17. Richards, RI
      Fragile and unstable chromosomes in cancer: causes and consequences

      TRENDS IN GENETICS
    18. Gursky, S; Olopade, OI; Rowley, JD
      Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types

      CANCER GENETICS AND CYTOGENETICS
    19. Hildebrandt, F; Rensing, C; Betz, RC; Sommer, U; Birnbaum, S; Imm, A; Omran, H; Leipoldt, M; Otto, E
      Establishing an algorithm for molecular genetic diagnostics in 127 families with juvenile nephronophthisis

      KIDNEY INTERNATIONAL
    20. Lucking, CB; Bonifati, V; Periquet, M; Vanacore, N; Brice, A; Meco, G
      Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

      NEUROLOGY
    21. Terreni, L; Calabrese, E; Calella, AM; Forloni, G; Mariani, C
      New mutation (RA2P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism

      NEUROLOGY
    22. Grady, B; Goharderakhshan, R; Chang, J; Ribeiro, LA; Perinchery, G; Franks, J; Presti, J; Carroll, P; Dahiya, R
      Frequently deleted loci on chromosome 9 may harbor several tumor suppressor genes in human renal cell carcinoma

      JOURNAL OF UROLOGY
    23. Gruttgen, A; Reichenzeller, M; Junger, M; Schlien, S; Affolter, A; Bosch, FX
      Detailed gene expression analysis but not microsatellite marker analysis of 9p21 reveals differential defects in the INK4a gene locus in the majorityof head and neck cancers

      JOURNAL OF PATHOLOGY
    24. Bonifati, V; Lucking, CB; Fabrizio, E; Periquet, M; Meco, G; Brice, A
      Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    25. Kubo, S; Kitami, T; Noda, S; Shimura, H; Uchiyama, Y; Asakawa, S; Minoshima, S; Shimizu, N; Mizuno, Y; Hattori, N
      Parkin is associated with cellular vesicles

      JOURNAL OF NEUROCHEMISTRY
    26. Ausserlechner, MJ; Obexer, P; Wiegers, GJ; Hartmann, BL; Geley, S; Kofler, R
      The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels (vol 276, pg 10984, 2001)

      JOURNAL OF BIOLOGICAL CHEMISTRY
    27. Ausserlechner, MJ; Obexer, P; Wiegers, GJ; Hartmann, BL; Geley, S; Kofler, R
      The cell cycle inhibitor p16(INK4A) sensitizes lymphoblastic leukemia cells to apoptosis by physiologic glucocorticoid levels

      JOURNAL OF BIOLOGICAL CHEMISTRY
    28. Klaes, R; Friedrich, T; Spitkovsky, D; Ridder, R; Rudy, W; Petry, U; Dallenbach-Hellweg, G; Schmidt, D; Doeberitz, MV
      Overexpression of p16(ink4a) as a specific marker for dysplastic and neoplastic epithelial cells of the cervix uteri

      INTERNATIONAL JOURNAL OF CANCER
    29. Pollock, PM; Welch, J; Hayward, NK
      Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development

      CANCER RESEARCH
    30. Wong, DJ; Paulson, TG; Prevo, LJ; Galipeau, PC; Longton, G; Blount, PL; Reid, BJ
      p16(INK4a) lesions are common, early abnormalities that undergo clonal expansion in Barrett's metaplastic epithelium

      CANCER RESEARCH
    31. Chim, CS; Tam, CYY; Liang, R; Kwong, YL
      Methylation of p15 and p16 genes in adult acute leukemia - Lack of prognostic significance

      CANCER
    32. Ramakers-van Woerden, NL; Pieters, R; Slater, RM; Loonen, AH; Beverloo, HB; van Drunen, E; Heyman, M; Moreno, TC; Rots, MG; van Wering, ER; Kamps, WA; Janka-Schaub, GE; Veerman, AJP
      In vitro drug resistance and prognostic impact of p16(INK4A)/p15(INK4B) deletions in childhood T-cell acute lymphoblastic leukaemia

      BRITISH JOURNAL OF HAEMATOLOGY
    33. Dai, CH; Krantz, SB
      Inn-eased expression of the INK4a/ARF locus in polycythemia vera

      BLOOD
    34. Lee, SH; Kim, WH; Kim, HK; Woo, KM; Nam, HS; Kim, HS; Kim, JG; Cho, MH
      Altered expression of the fragile histidine triad gene in primary gastric adenocarcinomas

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    35. Bostrom, J; Meyer-Puttlitz, B; Wolter, M; Blaschke, B; Weber, RG; Lichter, P; Ichimura, K; Collins, VP; Reifenberger, G
      Alterations of the tumor suppressor genes CDKN2A (p16(INK4a)), p14(ARF), CDKN2B (p15(INK4b)), and CDKN2C (p18(INK4c)) in atypical and anaplastic meningiomas

      AMERICAN JOURNAL OF PATHOLOGY
    36. Nakayama, T; Taback, B; Turner, R; Morton, DL; Hoon, DSB
      Molecular clonality of in-transit melanoma metastasis

      AMERICAN JOURNAL OF PATHOLOGY
    37. Schraml, P; Struckmann, K; Bednar, R; Fu, WT; Gasser, T; Wilber, K; Kononen, J; Sauter, G; Mihatsch, MJ; Moch, H
      CDKN2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas - Evidence for a second tumor suppressor gene proximal to CDKN2A

      AMERICAN JOURNAL OF PATHOLOGY
    38. Periquet, M; Lucking, CB; Vaughan, JR; Bonifati, V; Durr, A; De Michele, G; Horstink, MW; Farrer, M; Illarioshkin, SN; Pollak, P; Borg, M; Brefel-Courbon, C; Denefle, P; Meco, G; Gasser, T; Breteler, MMB; Wood, NW; Agid, Y; Brice, A
      Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects

      AMERICAN JOURNAL OF HUMAN GENETICS
    39. Pateromichelakis, S; Lee, G; Langdon, JD; Partridge, M
      The FHIT gene in oral squamous cell carcinoma: allelic imbalance is frequent but cDNA aberrations are uncommon

      ORAL ONCOLOGY
    40. Chung, MY; Wu, JC; Chau, GY; Lui, WY; Tsay, SH; Chiang, H
      Preferentially deleted chromosome region 9p21 in large hepatocellular carcinomas

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    41. Cachia, AR; Indsto, JO; McLaren, KM; Mann, GJ; Arends, MJ
      CDKN2A mutation and deletion status in thin and thick primary melanoma

      CLINICAL CANCER RESEARCH
    42. Hui, R; Macmillan, RD; Kenny, FS; Musgrove, EA; Blamey, RW; Nicholson, RI; Robertson, JFR; Sutherland, RL
      INK4a gene expression and methylation in primary breast cancer: Overexpression of p16(INK4a) messenger RNA is a marker of poor prognosis

      CLINICAL CANCER RESEARCH
    43. Omura-Minamisawa, M; Diccianni, MB; Batova, A; Chang, RC; Bridgeman, LJ; Yu, J; Pullen, J; Bowman, WP; Yu, AL
      Universal inactivation of both p16 and p15 but not downstream components is an essential event in the pathogenesis of T-cell acute lymphoblastic leukemia

      CLINICAL CANCER RESEARCH
    44. Baffa, R; Santoro, R; Bullrich, F; Mandes, B; Ishii, H; Croce, CM
      Definition and refinement of chromosome 8p regions of loss of heterozygosity in gastric cancer

      CLINICAL CANCER RESEARCH
    45. Seelan, RS; Qian, CP; Yokomizo, A; Bostwick, DG; Smith, DI; Liu, WG
      Human acid ceramidase is overexpressed but not mutated in prostate cancer

      GENES CHROMOSOMES & CANCER
    46. Arcellana-Panlilio, MY; Egeler, AM; Ujack, E; Pinto, A; Demetrick, DJ; Robbins, SM; Coppes, MJ
      Decreased expression of the INK4 family of cyclin-dependent kinase inhibitors in Wilms tumor

      GENES CHROMOSOMES & CANCER
    47. Hilgers, W; Koerkamp, BG; Geradts, J; Tang, DJ; Yeo, CJ; Hruban, RH; Kern, SE
      Genomic FHIT analysis in RER+ and RER- adenocarcinomas of the pancreas

      GENES CHROMOSOMES & CANCER
    48. Yoshinouchi, M; Hongo, A; Takamoto, N; Ono, Y; Nagao, S; Miyagi, Y; Kudo, T; Kodama, J
      Alteration of the CDKN2/p16 gene is not required for HPV-positive uterine cervical cancer cell lines

      INTERNATIONAL JOURNAL OF ONCOLOGY
    49. Kahle, PJ; Leimer, U; Haass, C
      Does failure of parkin-mediated ubiquitination cause juvenile parkinsonism?

      TRENDS IN BIOCHEMICAL SCIENCES
    50. Puig, S; Castro, J; Ventura, PJ; Ruiz, A; Ascaso, C; Melvehy, J; Estivill, X; Mascaro, JM; Lecha, M; Castel, T
      Large deletions of chromosome 9p in cutaneous malignant melanoma identify patients with a high risk of developing metastases

      MELANOMA RESEARCH
    51. Louhelainen, J; Wijkstrom, H; Hemminki, K
      Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer

      EUROPEAN JOURNAL OF CANCER
    52. D'Agata, V; Grimaldi, M; Pascale, A; Cavallaro, S
      Regional and cellular expression of the parkin gene in the rat cerebral cortex

      EUROPEAN JOURNAL OF NEUROSCIENCE
    53. Schmid, M; Sen, M; Rosenbach, MD; Carrera, CJ; Friedman, H; Carson, DA
      A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer

      ONCOGENE
    54. Steiner, MS; Wang, Y; Zhang, Y; Zhang, XW; Lu, Y
      p16/MTS1/INK4A suppresses prostate cancer by both pRb dependent and independent pathways

      ONCOGENE
    55. Steiner, MS; Zhang, Y; Farooq, F; Lerner, J; Wang, Y; Lu, Y
      Adenoviral vector containing wild-type p16 suppresses prostate cancer growth and prolongs survival by inducing cell senescence

      CANCER GENE THERAPY
    56. Wada, M; Okamura, T; Okada, M; Teramura, M; Masuda, M; Motoji, T; Mizoguchi, H
      Delineation of the frequently deleted region on chromosome arm 13q in B-cell non-Hodgkin's lymphoma

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    57. M'soka, TJ; Nishioka, J; Taga, A; Kato, K; Kawasaki, H; Yamada, Y; Yu, A; Komada, Y; Nobori, T
      Detection of methylthioadenosine phosphorylase (MTAP) and p16 gene deletion in T cell acute lymphoblastic leukemia by real-time quantitative PCR assay

      LEUKEMIA
    58. Gonzalez, M; Mateos, MV; Garcia-Sanz, R; Balanzategui, A; Lopez-Perez, R; Chillon, MC; Gonzalez, D; Alaejos, I; San Miguel, JF
      De novo methylation of tumor suppressor gene p16/INK4a is a frequent finding in multiple myeloma patients at diagnosis

      LEUKEMIA
    59. Durr, A; Lucking, C; Brice, A
      Parkin gene mutations and Parkinson's disease

      M S-MEDECINE SCIENCES
    60. Yamamura, Y; Hattori, N; Matsumine, H; Kuzuhara, S; Mizuno, Y
      Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification

      BRAIN & DEVELOPMENT
    61. Saito, M; Maruyama, M; Ikeuchi, K; Kondo, H; Ishikawa, A; Yuasa, T; Tsuji, S
      Autosomal recessive juvenile parkinsonism

      BRAIN & DEVELOPMENT
    62. Maruyama, M; Ikeuchi, T; Saito, M; Ishikawa, A; Yuasa, T; Tanaka, H; Hayashi, S; Wakabayashi, K; Takahashi, H; Tsuji, S
      Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism

      ANNALS OF NEUROLOGY
    63. Riess, O; Kuhn, W; Kruger, R
      Genetic influence on the development of Parkinson's disease

      JOURNAL OF NEUROLOGY
    64. Tunca, B; Egeli, U; Zorluoglu, A; Yilmazlar, T; Yerci, O; Kizil, A
      The expression of fragile sites in lymphocytes of patients with rectum cancer and their first-degree relatives

      CANCER LETTERS
    65. Chen, TC; Hsieh, LL; Kuo, TT; Ng, KF; Chou, YHW; Jeng, LB; Chen, MF
      p16(INK4) gene mutation and allelic loss of chromosome 9p21-22 in Taiwanese hepatocellular carcinoma

      ANTICANCER RESEARCH
    66. Brauers, A; Jakse, G
      Epidemiology and biology of human urinary bladder cancer

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    67. D'Agata, V; Zhao, WQ; Cavallaro, S
      Cloning and distribution of the rat parkin mRNA

      MOLECULAR BRAIN RESEARCH
    68. Leuraud, P; Marie, Y; Robin, E; Huguet, S; He, J; Mokhtari, K; Cornu, P; Khe, HX; Sanson, M
      Frequent loss of 1p32 region but no mutation if the p18 tumor suppressor gene in meningiomas

      JOURNAL OF NEURO-ONCOLOGY
    69. Guo, SX; Taki, T; Ohnishi, H; Piao, HY; Tabuchi, K; Bessho, F; Hanada, R; Yanagisawa, M; Hayashi, Y
      Hypermethylation of p16 and p15 genes and RB protein expression in acute leukemia

      LEUKEMIA RESEARCH
    70. Muscheck, M; Abol-Enein, H; Chew, K; Moore, D; Bhargava, V; Ghoneim, MA; Carroll, PR; Waldman, FM
      Comparison of genetic changes in schistosome-related transitional and squamous bladder cancers using comparative genomic hybridization

      CARCINOGENESIS
    71. Viallet, F
      Diagnostic criteria for idiopathic Parkinson's disease.

      REVUE NEUROLOGIQUE
    72. Lucking, CB; Durr, A; Bonifati, V; Vaughan, J; De Michele, G; Gasser, T; Harhangi, BS; Meco, G; Denefle, P; Wood, NW; Agid, Y; Brice, A
      Association between early-onset Parkinson's disease and mutations in the parkin gene

      NEW ENGLAND JOURNAL OF MEDICINE
    73. He, J; Hoang-Xuan, K; Marie, Y; Leuraud, P; Mokhtari, K; Kujas, M; Delattre, JY; Sanson, M
      P18 tumor suppressor gene and progression of oligodendrogliomas to anaplasia

      NEUROLOGY
    74. Schraml, P; Muller, D; Bednar, R; Gasser, T; Sauter, G; Mihatsch, MJ; Moch, H
      Allelic loss at the D9S171 focus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma

      JOURNAL OF PATHOLOGY
    75. Gu, WJ; Abbas, N; Lagunes, MZ; Parent, A; Pradier, L; Bohme, GA; Agid, Y; Hirsch, EC; Raisman-Vozari, R; Brice, A
      Cloning of rat parkin cDNA and distribution of parkin in rat brain

      JOURNAL OF NEUROCHEMISTRY
    76. Bortolotto, S; Chiado-Piat, L; Cavalla, P; Bosone, I; Chio, A; Mauro, A; Schiffer, D
      CDKN2A/p16 inactivation in the prognosis of oligodendrogliomas

      INTERNATIONAL JOURNAL OF CANCER
    77. Hu, CJ; Sung, SM; Liu, HC; Lee, CC; Tsai, CH; Chang, JG
      Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan

      EUROPEAN NEUROLOGY
    78. Eissa, S; Ali-Labib, R; Khalifa, A
      Deletion of p16 and p15 genes In schistosomiasis-associated bladder cancer(SABC)

      CLINICA CHIMICA ACTA
    79. Kholodnyuk, ID; Szeles, A; Yang, Y; Klein, G; Imreh, S
      Inactivation of the human fragile histidine triad gene at 3p14.2 in monochromosomal human/mouse microcell hybrid-derived severe combined immunodeficient mouse tumors

      CANCER RESEARCH
    80. Tang, BQ; Li, YNN; Kruger, WD
      Defects in methylthioadenosine phosphorylase are associated with but not responsible for methionine-dependent tumor cell growth

      CANCER RESEARCH
    81. Sarkar, S; Julicher, KP; Burger, MS; Della Valle, V; Larsen, CJ; Yeager, TR; Grossman, TB; Nickells, RW; Protzel, C; Jarrard, DF; Reznikoff, CA
      Different combinations of genetic/epigenetic alterations inactivate the p53 and pRb pathways in invasive human bladder cancers

      CANCER RESEARCH
    82. Baek, MJ; Piao, Z; Park, C; Shin, EC; Park, JH; Jung, HJ; Kim, CG; Kim, H
      p16 is a major inactivation target in hepatocellular carcinoma

      CANCER
    83. Palmieri, G; Cossu, A; Ascierto, PA; Botti, G; Strazzullo, M; Lissia, A; Colombino, M; Casula, M; Floris, C; Tanda, F; Pirastu, M; Castello, G
      Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases

      BRITISH JOURNAL OF CANCER
    84. Wong, IHN; Ng, MHL; Huang, DP; Lee, JCK
      Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: potential prognostic implications

      BLOOD
    85. Hung, KS; Hong, CY; Lee, JH; Lin, SK; Huang, SC; Wang, TM; Tse, V; Sliverberg, GD; Weng, SC; Hsiao, M
      Expression of p16(INK4A) induces dominant suppression of glioblastoma growth in situ through necrosis and cell cycle arrest

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    86. Yatsuoka, T; Sunamura, M; Furukawa, T; Fukushige, S; Yokoyama, T; Inoue, H; Shibuya, K; Takeda, K; Matsuno, S; Horii, A
      Association of poor prognosis with loss of 12q, 17p, and 18q, and concordant loss of 6q/17p and 12q/18q in human pancreatic ductal adenocarcinoma

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    87. Brice, A
      Genome and neurology - The example of Parkinson's disease

      BULLETIN DE L ACADEMIE NATIONALE DE MEDECINE
    88. Gruis, NA; van der Velden, PA; Bergman, W; Frants, RR
      Familial melanoma; CDKN2A and beyond

      JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS
    89. Hallas, C; Albitar, M; Letofsky, J; Keating, MJ; Huebner, K; Croce, CM
      Loss of FHIT expression in acute lymphoblastic leukemia

      CLINICAL CANCER RESEARCH
    90. Faderl, S; Kantarjian, HM; Manshouri, T; Chan, CY; Pierce, S; Hays, KJ; Cortes, J; Thomas, D; Estrov, Z; Albitar, M
      The prognostic significance of p16(INK4a)/p14(ARF) and p15(INK4b) deletions in adult acute lymphoblastic leukemia

      CLINICAL CANCER RESEARCH
    91. Gramantieri, L; Chieco, P; Di Tomaso, M; Masi, L; Piscaglia, F; Brillanti, S; Gaiani, S; Valgimigli, M; Mazziotti, A; Bolondi, L
      Aberrant fragile histidine triad gene transcripts in primary hepatocellular carcinoma and liver cirrhosis

      CLINICAL CANCER RESEARCH
    92. Hilgers, W; Kern, SE
      Molecular genetic basis of pancreatic adenocarcinoma

      GENES CHROMOSOMES & CANCER
    93. Sato, H; Hiyama, K; Ishioka, S; Maeda, H; Yamakido, M
      Alternative splicing, but not allelic loss, of the FHIT gene increases with development of lung cancer

      INTERNATIONAL JOURNAL OF ONCOLOGY
    94. Junker, K; Werner, W; Mueller, C; Ebert, W; Schubert, J; Claussen, U
      Interphase cytogenetic diagnosis of bladder cancer on cells from urine andbladder washing

      INTERNATIONAL JOURNAL OF ONCOLOGY
    95. Lee, WC; Testa, JR
      Somatic genetic alterations in human malignant mesothelioma (Review)

      INTERNATIONAL JOURNAL OF ONCOLOGY
    96. Kumar, R; Smeds, J; Rozell, BL; Hemminki, K
      Loss of heterozygosity at chromosome 9p21 (INK4-p14(ARF) locus): homozygous deletions and mutations in the p16 and p14(ARF) genes in sporadic primarymelanomas

      MELANOMA RESEARCH
    97. Rizos, H; Darmanian, AP; Indsto, JO; Shannon, JA; Kefford, RF; Mann, GJ
      Multiple abnormalities of the p16(INK4a)-pRb regulatory pathway in cultured melanoma cells

      MELANOMA RESEARCH
    98. Satoh, J; Kuroda, Y
      Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease

      NEUROREPORT
    99. Liew, CT; Li, HM; Lo, KW; Leow, CK; Chan, JYH; Hin, LY; Lau, WY; Lai, PBS; Lim, BK; Huang, J; Leung, WT; Wu, S; Lee, JCK
      High frequency of p16(INK4A) gene alterations in hepatocellular carcinoma

      ONCOGENE
    100. Fujimoto, A; Morita, R; Hatta, N; Takehara, K; Takata, M
      p16(INK4a) inactivation is not frequent in uncultured sporadic primary cutaneous melanoma

      ONCOGENE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 18/01/21 alle ore 06:19:40