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    1. Simsir, A; Palacios, D; Linehan, WM; Merino, MJ; Abati, A
      Detection of loss of heterozygosity at chromosome 3p25-26 in primary and metastatic ovarian clear-cell carcinoma: Utilization of microdissection and polymerase chain reaction in archival tissues

      DIAGNOSTIC CYTOPATHOLOGY
    2. Zhang, D; Cupp, MS; Cupp, EW
      Polymorphism of the thrombostasin gene in the horn fly (Haematobia irritans) revealed in a cDNA library and in genomic DNA

      MOLECULAR GENETICS AND GENOMICS
    3. Alves, PC; Ferrand, N; Suchentrunk, F
      Developmental stability and protein heterozygosity in a local population of Iberian hares (Lepus granatensis)

      MAMMALIAN BIOLOGY
    4. Smith, MH; Novak, JM; Peles, JD; Purdue, JR
      Genetic heterogeneity of white-tailed deer: management lessons from a long-term study

      MAMMALIAN BIOLOGY
    5. Suchentrunk, F; Jaschke, C; Haiden, A
      Little allozyme and mtDNA variability in brown hares (Lepus europaeus) from New Zealand and Britain - A legacy of bottlenecks?

      MAMMALIAN BIOLOGY
    6. Lockett, SF; Robertson, JR; Brettle, RP; Yap, PL; Middleton, D; Brown, AJL
      Mismatched human leukocyte antigen alleles protect against heterosexual HIV transmission

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    7. El-Rifai, W; Rutherford, S; Knuutila, S; Frierson, HF; Moskaluk, CA
      Novel DNA copy number losses in chromosome 12q12-q13 in adenoid cystic carcinoma

      NEOPLASIA
    8. Skotheim, RI; Kraggerud, SM; Fossa, SD; Stenwig, AE; Gedde-Dahl, T; Danielsen, HE; Jakobsen, KS; Lothe, RA
      Familial/bilateral and sporadic testicular germ cell tumors show frequent genetic changes at loci with suggestive linkage evidence

      NEOPLASIA
    9. Pertoldi, C; Scali, V; Loeschcke, V
      Developmental instability in sexually reproducing and parthenogenetic populations of Bacillus rossius rossius and Bacillus rossius redtenbacheri

      EVOLUTIONARY ECOLOGY RESEARCH
    10. Mazurier, C; Goudemand, J; Hilbert, L; Caron, C; Fressinaud, E; Meyer, D
      Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    11. Renesto, E; Zawadzki, CH; Revaldaves, E
      Biochemical taxonomy of Crenicichla (Pisces : Perciformes : Cichlidae) of the Iguacu River, Brazil

      BRAZILIAN ARCHIVES OF BIOLOGY AND TECHNOLOGY
    12. Noone, PG; Knowles, MR
      'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations

      RESPIRATORY RESEARCH
    13. Kittiniyom, K; Gorse, KM; Dalbegue, F; Lichy, JH; Taubenberger, JK; Newsham, IF
      Allelic loss on chromosome band 18p11.3 occurs early and reveals heterogeneity in breast cancer progression

      BREAST CANCER RESEARCH
    14. Wada, T; Louhelainen, J; Hemminki, K; Adolfsson, J; Wijkstrom, H; Norming, U; Borgstrom, E; Hansson, J; Steineck, G
      The prevalence of loss of heterozygosity in chromosome 3, including FHIT, in bladder cancer, using the fluorescent multiplex polymerase chain reaction

      BJU INTERNATIONAL
    15. van der Velde, M; Bijlsma, R
      Genetic evidence for the allodiploid origin of the moss species Polytrichum longisetum

      PLANT BIOLOGY
    16. Mizutani, M; Yamamoto, T; Torii, K; Kawase, H; Yoshimoto, T; Uchihi, R; Tanaka, M; Tamaki, K; Katsumata, Y
      Analysis of 168 short tandem repeat loci in the Japanese population, usinga screening set for human genetic mapping

      JOURNAL OF HUMAN GENETICS
    17. Kayahara, H; Yamagata, H; Tanioka, H; Miki, T; Hamakawa, H
      Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

      JOURNAL OF HUMAN GENETICS
    18. Ikari, K; Onda, H; Furushima, K; Maeda, S; Harata, S; Takeda, J
      Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population

      JOURNAL OF HUMAN GENETICS
    19. Harada, H; Nagai, NH; Tsuneizumi, M; Mikami, I; Sugano, S; Emi, M
      Identification of DMC1, a novel gene in the TOC region on 17q25.1 that shows loss of expression in multiple human cancers

      JOURNAL OF HUMAN GENETICS
    20. Druck, T; Podolski, J; Byrski, T; Wyrwicz, L; Zajaczek, S; Kata, G; Borowka, A; Lubinski, J; Huebner, K
      The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

      JOURNAL OF HUMAN GENETICS
    21. Murata, M; Miyoshi, Y; Iwao, K; Wada, H; Shibata, K; Tateishi, H; Shimano, T; Ohasawa, M; Imai, Y; Nishikawa, M; Kobayashi, T
      Combined hepatocellular/cholangiocellular carcinoma with sarcomatoid features: genetic analysis for histogenesis

      HEPATOLOGY RESEARCH
    22. Kishimoto, Y; Morisawa, T; Kitano, M; Shiota, G; Horie, Y; Suou, T; Ito, H; Kawasaki, H; Hasegawa, J
      Loss of heterozygosity of the mannose 6-phosphate/insulin-like growth factor II receptor and p53 genes in human hepatocellular carcinoma

      HEPATOLOGY RESEARCH
    23. Domon, OE; McGarrity, LJ; Bishop, M; Yoshioka, M; Chen, JJ; Morris, SM
      Evaluation of the genotoxicity of the phytoestrogen, coumestrol, in AHH-1 TK+/- human lymphoblastoid cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    24. Wijnhoven, SWP; Kool, HJM; van Teijlingen, CMM; van Zeeland, AA; Vrieling, H
      Loss of heterozygosity in somatic cells of the mouse - An important step in cancer initiation?

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    25. Honma, M; Momose, M; Sakamoto, H; Sofuni, T; Hayashi, M
      Spindle poisons induce allelic loss in mouse lymphoma cells through mitotic non-disjunction

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    26. Zhang, L; Poh, CF; Lam, WL; Epstein, JB; Cheng, X; Zhang, X; Priddy, R; Lovas, J; Le, ND; Rosin, MP
      Impact of localized treatment in reducing risk of progression of low-gradeoral dysplasia: molecular evidence of incomplete resection

      ORAL ONCOLOGY
    27. 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
    28. O'Connor, DP; Kay, EW; Leader, M; Murphy, GM; Atkins, GJ; Mabruk, MJEMF
      A high degree of chromosomal instability at 13q14 in cutaneous squamous cell carcinomas: indication for a role of a tumour suppressor gene other thanRb

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    29. Granerus, M; Johannisson, A; Ekblom, P; Engstrom, W
      Insulin-like growth factors I and II induce cell death in Wilms's tumour cells

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    30. Appleyard, SA; Renwick, JM; Mather, PB
      Individual heterozygosity levels and relative growth performance in Oreochromis niloticus (L.) cultured under Fijian conditions

      AQUACULTURE RESEARCH
    31. Campbell, IG; Thomas, EJ
      Endometriosis: candidate genes

      HUMAN REPRODUCTION UPDATE
    32. Citek, J; Rehout, V
      Evaluation of the genetic diversity in cattle using microsatellites and protein markers

      CZECH JOURNAL OF ANIMAL SCIENCE
    33. Packer, L; Owen, R
      Population genetic aspects of pollinator decline

      CONSERVATION ECOLOGY
    34. Zarattini, P; Magnaschi, G; Rossi, V; Mura, G
      Further evidence of the synonymy between Branchipus schaefferi and B-visnyai (Crustacea, Anostraca)

      ITALIAN JOURNAL OF ZOOLOGY
    35. Vassilakis, DA; Sourvinos, G; Pantelidis, P; Spandidos, DA; Siafakas, NM; Bouros, D
      Extended genetic alterations in a patient with pulmonary sarcoidosis, a benign disease

      SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES
    36. Katoh, M
      Molecular cloning and characterization of LZIC, a novel gene encoding ICAThomologous protein with leucine zipper domain

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    37. Sossey-Alaoui, K; Kitamura, E; Cowell, JK
      Fine mapping of the PTGFR gene to 1p31 region and mutation analysis in human breast cancer

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    38. Imai, FL; Uzawa, K; Miyakawa, A; Shiiba, M; Tanzawa, H
      A detailed deletion map of chromosome 20 in human oral squamous cell carcinoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    39. Tonini, GP; McConville, C; Cusano, R; Rees, SA; Dagnino, M; Longo, L; De Bernardi, B; Conte, M; Garaventa, A; Romeo, G; Devoto, M; Seri, M
      Exclusion of candidate genes and chromosomal regions in familial neuroblastoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    40. Vladutiu, GD
      Heterozygosity: An expanding role in proteomics

      MOLECULAR GENETICS AND METABOLISM
    41. Smith, AC; Squire, JA; Thorner, P; Zielenska, M; Shuman, C; Grant, R; Chitayat, D; Nishikawa, JL; Weksberg, R
      Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    42. Kroken, S; Taylor, JW
      Outcrossing and recombination in the lichenized fungus Letharia

      FUNGAL GENETICS AND BIOLOGY
    43. Liao, PH; Lee, TL; Yang, LC; Yang, SH; Chen, SL; Chou, MY
      Adenomatous polyposis coli gene mutation and decreased wildtype p53 protein expression in oral submucous fibrosis: A preliminary investigation

      ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS
    44. 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
    45. Gong, G; DeVries, S; Chew, KL; Cha, I; Ljung, BM; Waldman, FM
      Genetic changes in paired atypical and usual ductal hyperplasia of the breast by comparative genomic hybridization

      CLINICAL CANCER RESEARCH
    46. Virmani, AK; Rathi, A; Sathyanarayana, UG; Padar, A; Huang, CX; Cunnigham, HT; Farinas, AJ; Milchgrub, S; Euhus, DM; Gilcrease, M; Herman, J; Minna, JD; Gazdar, AF
      Aberrant methylation of the adenomatous polyposis coli (APC) gene promoter1A in breast and lung carcinomas

      CLINICAL CANCER RESEARCH
    47. Vecchione, A; Ishii, H; Shiao, YH; Trapasso, F; Rugge, M; Tamburrino, JF; Murakumo, Y; Alder, H; Croce, CM; Baffa, R
      Fez1/Lzts1 alterations in gastric carcinoma

      CLINICAL CANCER RESEARCH
    48. Hirano, A; Emi, M; Tsuneizumi, M; Utada, Y; Yoshimoto, M; Kasumi, F; Akiyama, F; Sakamoto, G; Haga, S; Kajiwara, T; Nakamura, Y
      Allelic losses of loci at 3p25.1, 8p22, 13q12, 17p13.3, and 22q13 correlate with postoperative recurrence in breast cancer

      CLINICAL CANCER RESEARCH
    49. Boyle, JO; Lonardo, F; Chang, JH; Klimstra, D; Rusch, V; Dmitrovsky, E
      Multiple high-grade bronchial dysplasia and squamous cell carcinoma: Concordant and discordant mutations

      CLINICAL CANCER RESEARCH
    50. Tibiletti, MG; Bernasconi, B; Furlan, D; Bressan, P; Cerutti, R; Facco, C; Franchi, M; Riva, C; Cinquetti, R; Capella, C; Taramelli, R
      Chromosome 6 abnormalities in ovarian surface epithelial tumors of borderline malignancy suggest a genetic continuum in the progression model of ovarian neoplasms

      CLINICAL CANCER RESEARCH
    51. Manne, U; Gary, BD; Oelschlager, DK; Weiss, HL; Frost, AR; Grizzle, WE
      Altered subcellular localization of suppressin, a novel inhibitor of cell-cycle entry, is an independent prognostic factor in colorectal adenocarcinomas

      CLINICAL CANCER RESEARCH
    52. Yu, J; Astrinidis, A; Henske, EP
      Chromosome 16 loss of heterozygosity in tuberous sclerosis and sporadic lymphangiomyomatosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    53. Chan, JKC; Wong, CSC
      Loss of E-cadherin is the fundamental defect in diffuse-type gastric carcinoma and infiltrating lobular carcinoma of the breast

      ADVANCES IN ANATOMIC PATHOLOGY
    54. Maluf, H; Koerner, F
      Lobular carcinoma in situ and infiltrating ductal carcinoma: Frequent presence of DCIS as a precursor lesion

      INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY
    55. Man, YG; Mannion, C; Kuhls, E; Moinfar, F; Bratthauer, GL; Albores-Saavedra, J; Tavassoli, FA
      Allelic losses at 3p and 11p are detected in both epithelial and stromal components of cervical small-cell neuroendocrine carcinoma

      APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY
    56. Thomas, NA; Choong, DYH; Jokubaitis, VJ; Neville, PJ; Campbell, IG
      Mutation of the ST7 tumor suppressor gene on 7q31.1 is rare in breast, ovarian and colorectal cancers

      NATURE GENETICS
    57. Serra, E; Rosenbaum, T; Nadal, M; Winner, U; Ars, E; Estivill, X; Lazaro, C
      Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas

      NATURE GENETICS
    58. Zenklusen, JC; Conti, CJ; Green, ED
      Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31

      NATURE GENETICS
    59. Kuramochi, M; Fukuhara, H; Nobukuni, T; Kanbe, T; Maruyama, T; Ghosh, HP; Pletcher, M; Isomura, M; Onizuka, M; Kitamura, T; Sekiya, T; Reeves, RH; Murakami, Y
      TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer

      NATURE GENETICS
    60. Goldrick, MM
      RNase cleavage-based methods for mutation/SNP detection, past and present

      HUMAN MUTATION
    61. Deltas, CC
      Mutations of the human polycystic kidney disease 2 (PKD2) gene

      HUMAN MUTATION
    62. Bretagnolle, F; Thompson, JD
      Phenotypic plasticity in sympatric diploid and autotetraploid Dactylis glomerata

      INTERNATIONAL JOURNAL OF PLANT SCIENCES
    63. Maggioni, R; Rogers, AD; Maclean, N; D'Incao, F
      Molecular phylogeny of western Atlantic Farfantepenaeus and Litopenaeus shrimp based on mitochondrial 16S partial sequences

      MOLECULAR PHYLOGENETICS AND EVOLUTION
    64. Bovee, JVMG; Sciot, R; Cin, PD; Debiec-Rychter, M; van Zelderen-Bhola, SL; Cornelisse, CJ; Hogendoorn, PCW
      Chromosome 9 alterations and trisomy 22 in central chondrosarcoma: A cytogenetic and DNA flow cytometric analysis of chondrosarcoma subtypes

      DIAGNOSTIC MOLECULAR PATHOLOGY
    65. Moreno-Bueno, G; Gamallo, C; Perez-Gallego, L; de Mora, JC; Suarez, A; Palacios, J
      beta-catenin expression pattern, beta-catenin gene mutations, and microsatellite instability in endometrioid ovarian carcinomas and synchronous endometrial carcinomas

      DIAGNOSTIC MOLECULAR PATHOLOGY
    66. Alonso, J; Garcia-Miguel, P; Abelairas, J; Mendiola, M; Pestana, A
      A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RBI locus in retinoblastoma and osteosarcoma

      DIAGNOSTIC MOLECULAR PATHOLOGY
    67. Amant, F; Dorfling, CM; Dreyer, L; Vergote, I; Lindeque, BG; Van Rensburg, EJ
      Microsatellite instability in uterine sarcomas

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER
    68. Wiest, J; Clark, AM; Dai, W
      Intron/exon organization and polymorphisms of the PLK3/PRK gene in human lung carcinoma cell lines

      GENES CHROMOSOMES & CANCER
    69. Deblec-Rychter, M; Sciot, R; Pauwels, P; Schoenmakers, E; Dal Cin, P; Hagemeijer, A
      Molecular cytogenetic definition of three distinct chromosome arm 14q deletion intervals in gastrointestinal stromal tumors

      GENES CHROMOSOMES & CANCER
    70. Chen, YZ; Soeda, E; Yang, HW; Takita, J; Chai, L; Horii, A; Inazawa, J; Ohki, M; Hayashi, Y
      Homozygous deletion in a neuroblastoma cell line defined by a high-densitySTS map spanning human chromosome band 1p36

      GENES CHROMOSOMES & CANCER
    71. Li, G; Hu, N; Goldstein, AM; Tang, ZZ; Roth, MJ; Wang, QH; Dawsey, SM; Han, XY; Ding, T; Huang, J; Giffen, C; Taylor, PR; Emmert-Buck, MR
      Allelic loss on chromosome bands 13q1 1-q13 in esophageal squamous cell carcinoma

      GENES CHROMOSOMES & CANCER
    72. 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
    73. Perotti, D; Testi, MA; Mondini, P; Pilotti, S; Green, ED; Pession, A; Sozzi, G; Pierotti, MA; Fossati-Bellani, F; Radice, P
      Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours

      GENES CHROMOSOMES & CANCER
    74. Balsara, BR; Pei, JM; De Rienzo, A; Simon, D; Tosolini, A; Lu, YY; Shen, FM; Fan, XL; Lin, WY; Buetow, KH; London, WT; Testa, JR
      Human hepatocellular carcinoma is characterized by a highly consistent pattern of genomic imbalances, including frequent loss of 16q23.1-24.1

      GENES CHROMOSOMES & CANCER
    75. Fang, Y; Guan, XY; Guo, Y; Sham, JST; Deng, MQ; Liang, QW; Li, HM; Zhang, HG; Zhou, H; Trent, J
      Analysis of genetic alterations in primary nasopharyngeal carcinoma by comparative genomic hybridization

      GENES CHROMOSOMES & CANCER
    76. Piao, Z; Lee, KS; Kim, H; Perucho, M; Malkhosyan, S
      Identification of novel deletion regions on chromosome arms 2q and 6p in breast carcinomas by amplotype analysis

      GENES CHROMOSOMES & CANCER
    77. Caron, H; Spieker, N; Godfried, N; Veenstra, M; van Sluis, P; de Kraker, J; Voute, P; Versteeg, R
      Chromosome bands Ip35-36 contain two distinct neuroblastoma tumor suppressor loci, one of which is imprinted

      GENES CHROMOSOMES & CANCER
    78. Milinski, M; Wedekind, C
      Evidence for MHC-correlated perfume preferences in humans

      BEHAVIORAL ECOLOGY
    79. Rainho, CA; Kowalski, LP; Rogatto, SR
      Loss of imprinting and loss of heterozygosity on 11p15.5 in head and neck squamous cell carcinomas

      HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK
    80. Zhu, Y; Loukola, A; Monni, O; Kuokkanen, K; Franssila, K; Elonen, E; Vilpo, J; Joensuu, H; Kere, J; Aaltonen, L; Knuutila, S
      PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas

      LEUKEMIA & LYMPHOMA
    81. Ranjan, D; Kashyap, VK
      Genetic variation observed at three tetrameric short tandem repeat loci HumTHO1, TPOX, and CSF1PO - in five ethnic population groups of northeastern India

      AMERICAN JOURNAL OF HUMAN BIOLOGY
    82. Brown, I; Milner, BJ; Rooney, PH; Haites, NE
      Inactivation of the p16(INK4A) gene by methylation is not a frequent eventin sporadic ovarian carcinoma

      ONCOLOGY REPORTS
    83. Miyashita, H; Mori, S; Tanda, N; Nakayama, K; Kanzaki, A; Sato, A; Morikawa, H; Motegi, K; Takebayashi, Y; Fukumoto, M
      Loss of heterozygosity of nucleotide excision repair factors in sporadic oral squamous cell carcinoma using microdissected tissue

      ONCOLOGY REPORTS
    84. Iyoda, A; Hiroshima, K; Toyozaki, T; Baba, M; Fujisawa, T; Yusa, T; Ohwada, H
      Microsatellite alterations in patients with thoracic sarcoma

      ONCOLOGY REPORTS
    85. Ubagai, T; Matsuura, S; Tauchi, H; Itou, K; Komatsu, K
      Comparative genomic hybridization analysis suggests a gain of chromosome 7p associated with lymph node metastasis in non-small cell lung cancer

      ONCOLOGY REPORTS
    86. Murahashi, K; Yashiro, M; Takenaka, C; Matsuoka, T; Ohira, M; Chung, KHY
      Establishment of a new scirrhous gastric cancer cell line with loss of heterozygosity at E-cadherin locus

      INTERNATIONAL JOURNAL OF ONCOLOGY
    87. Shiozaki, K; Nakamori, S; Tsujie, M; Okami, J; Yamamoto, H; Nagano, H; Dono, K; Umeshita, K; Sakon, M; Furukawa, H; Hiratsuka, M; Kasugai, T; Ishiguro, S; Monden, M
      Human stomach-specific gene, CA11, is down-regulated in gastric cancer

      INTERNATIONAL JOURNAL OF ONCOLOGY
    88. Hoang, MP; Callender, DL; Gallego, JJS; Huang, Z; Sneige, N; Luna, MA; Batsakis, JG; El-Naggar, AK
      Molecular and biomarker analyses of salivary duct carcinomas: Comparison with mammary duct carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    89. Yang, EB; Zhao, YN; Zhang, K; Mack, P
      Microsatellite alterations in human hepatocellular carcinoma infected withhepatitis B virus: Associated with the elevation of serum alpha-fetoprotein

      INTERNATIONAL JOURNAL OF ONCOLOGY
    90. 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
    91. Sasiadek, M; Stembalska-Kozlowska, A; Smigiel, R; Krecicki, T; Blin, N; Mirghomizadeh, F
      Microsatellite and chromosome instability in squamous cell laryngeal carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    92. Takahashi, K; Kawamura, N; Tsujimura, A; Ichimura, T; Ito, F; Ishiko, O; Ogita, S
      Association of the shrinkage of uterine leiomyoma treated with GnRH agonist and deletion of long arm of chromosome 7

      INTERNATIONAL JOURNAL OF ONCOLOGY
    93. Nozaki, I; Ohashi, R; Matsubara, N; Hirai, R; Andou, A; Miyazaki, M; Shimizu, N; Namba, M
      Microsatellite instability correlates with normal expression of cyclin E in hepatocellular carcinomas

      INTERNATIONAL JOURNAL OF ONCOLOGY
    94. Harada, H; Uchida, N; Shimada, Y; Kumimoto, H; Shinoda, M; Imamura, M; Ishizaki, K
      Polymorphism and allelic loss at the AS3 locus on 13q12-13 in esophageal squamous cell carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    95. 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
    96. Nishioka, N; Yoshiro, M; Inoue, T; Matsuoka, T; Ohira, M; Chung, KH
      A candidate tumor suppressor locus for scirrhous gastric cancer at chromosome 18q 12.2

      INTERNATIONAL JOURNAL OF ONCOLOGY
    97. Louhelainen, J; Wijstrom, H; Hemminki, K
      Multiple regions with allelic loss at chromosome 3 in superficial multifocal bladder tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    98. Danarti, R; Happle, R; Konig, A
      Paradominant inheritance may explain familial occurrence of cutis marmorata telangiectatica congenital

      DERMATOLOGY
    99. Dos Santos, MR; Vieira, EM; Lima, MR
      Molecular diagnosis and counseling in a family presenting compound heterozygosity for autosomal recessive limb-girdle muscular dystrophy

      GENETIC COUNSELING
    100. Alexander, JM
      Tumor suppressor loss in pituitary tumors

      BRAIN PATHOLOGY


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Documento generato il 27/02/20 alle ore 16:19:25