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La ricerca find articoli where soggetti phrase all words 'MUTATION ANALYSIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 488 riferimenti
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    1. Wuyts, W; Van Wesenbeeck, L; Morales-Piga, A; Ralston, S; Hocking, L; Vanhoenacker, F; Westhovens, R; Verbruggen, L; Anderson, D; Hughes, A; Van Hul, W
      Evaluation of the role of RANK and OPG genes in Paget's disease of bone

      BONE
    2. Thakker, RV
      Molecular genetics and patient management of multiple endocrine neoplasia type I

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    3. Sharma, A; James, M; Donaldson, A; Fox, R
      Hereditary non-polyposis colorectal cancer syndrome: combined risk of gastrointestinal and gynaecological cancer

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    4. Namba, A; Abe, S; Shinkawa, H; Kimberling, WJ; Usami, S
      Genetic features of hearing loss associated with ear anomalies: PDS and EYA1 mutation analysis

      JOURNAL OF HUMAN GENETICS
    5. Ashley, GA; Shabbeer, J; Yasuda, M; Eng, CM; Desnick, RJ
      Fabry disease: twenty novel alpha-galactosidase A mutations causing the classical phenotype

      JOURNAL OF HUMAN GENETICS
    6. Clerici, T; Schmid, C; Komminoth, P; Lange, F; Spinas, GA; Brandle, M
      10 Swiss kindreds with multiple endocrine neoplasia type 1: assessment of screening methods

      SWISS MEDICAL WEEKLY
    7. Jacobi, FK; Meyer, J; Pusch, CM; Wissinger, B
      Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(R)(exo-) DNA polymerase and RFLP analysis

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    8. Acquila, M; Bottini, F; Valetto, A; Caprino, D; Mori, PG; Bicocchi, MP
      A new strategy for prenatal diagnosis in a sporadic haemophilia B family

      HAEMOPHILIA
    9. Oranwiroon, S; Akkarapatumwong, V; Pung-Amritt, P; Treesucon, A; Veerakul, G; Mahasandana, C; Panyim, S; Yenchitsomanus, P
      Determination of haemophilia A carrier status by mutation analysis

      HAEMOPHILIA
    10. Janecke, AR; Mayatepek, E; Utermann, G
      Molecular genetics of type 1 glycogen storage disease

      MOLECULAR GENETICS AND METABOLISM
    11. Wakefield, LM; Piek, E; Bottinger, EP
      TGF-beta signaling in mammary gland development and tumorigenesis

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    12. Papanikolaou, G; Politou, M; Roetto, A; Bosio, S; Sakelaropoulos, N; Camaschella, C; Loukopoulos, D
      Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

      BLOOD CELLS MOLECULES AND DISEASES
    13. Zanella, A; Bianchi, P; Iurlo, A; Boschetti, C; Taioli, E; Vercellati, C; Zappa, M; Fermo, E; Tavazzi, D; Sampietro, M
      Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: Study of Italian cases

      BLOOD CELLS MOLECULES AND DISEASES
    14. Muro-Cacho, CA; Rosario-Ortiz, K; Livingston, S; Munoz-Antonia, T
      Defective transforming growth factor beta signaling pathway in head and neck squamous cell carcinoma as evidenced by the lack of expression of activated Smad2

      CLINICAL CANCER RESEARCH
    15. Bravo, J; Li, Z; Speck, NA; Warren, AJ
      The leukemia-associated AML1 (Runx1)-CBF beta complex functions as a DNA-induced molecular clamp

      NATURE STRUCTURAL BIOLOGY
    16. Gregersen, N; Andresen, BS; Corydon, M; Corydon, TJ; Olsen, RKJ; Bolund, L; Bross, P
      Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship

      HUMAN MUTATION
    17. Heino, M; Peterson, P; Kudoh, J; Shimizu, N; Antonarakis, SE; Scott, HS; Krohn, K
      APECED mutations in the autoimmune regulator (AIRE) gene

      HUMAN MUTATION
    18. Cihakova, D; Trebusak, K; Heino, M; Fadeyev, V; Tiulpakov, A; Battelino, T; Tar, A; Halasz, Z; Blumel, P; Tawfik, S; Krohn, K; Lebl, J; Peterson, P
      Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED

      HUMAN MUTATION
    19. Masmoudi, S; Antonarakis, SE; Schwede, T; Ghorbel, AM; Gratri, M; Pappasavas, MP; Drira, M; Elgaied-Boutila, A; Wattenhofer, M; Rossier, C; Scott, HS; Ayadi, H; Guipponi, M
      Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

      HUMAN MUTATION
    20. Miano, MG; Testa, F; Filippini, F; Trujillo, M; Conte, I; Lanzara, C; Millan, JM; De Bernardo, C; Grammatico, B; Mangino, M; Torrente, I; Carrozzo, R; Simonelli, F; Rinaldi, E; Ventruto, V; D'Urso, M; Ayuso, C; Ciccodicola, A
      Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains

      HUMAN MUTATION
    21. Bar, J; Linke, T; Ferlinz, K; Neumann, U; Schuchman, EH; Sandhoff, K
      Molecular analysis of acid ceramidase deficiency in patients with Farber disease

      HUMAN MUTATION
    22. Acosta, AX; Silva, WA; Carvalho, TM; Gomes, M; Zago, MA
      Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria

      HUMAN MUTATION
    23. Sohocki, MM; Daiger, SP; Bowne, SJ; Rodriguez, JA; Northrup, H; Heckenlively, JR; Birch, DG; Mintz-Hittner, H; Ruiz, RS; Lewis, RA; Saperstein, DA; Sullivan, LS
      Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

      HUMAN MUTATION
    24. Mori, M; Kida, H; Morishita, H; Goya, S; Matsuoka, H; Arai, T; Osaki, T; Tachibana, I; Yamamoto, S; Sakatani, M; Ito, M; Ogura, T; Hayashi, S
      Microsatellite instability in transforming growth factor-beta 1 type II receptor gene in alveolar lining epithelial cells of idiopathic pulmonary fibrosis

      AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
    25. Bjorheim, J; Gaudernack, G; Ekstrom, PO
      Mutation analysis of TP53 exons 5-8 by automated constant denaturant capillary electrophoresis

      TUMOR BIOLOGY
    26. Xia, JH; Zheng, D; Tang, DS; Dai, HP; Pan, Q; Long, ZG; Liao, XD
      Cloning, mapping and mutation analysis of human gene GJB5 encoding gap junction protein beta-5

      SCIENCE IN CHINA SERIES C-LIFE SCIENCES
    27. Pogue, R; Anderson, LVB; Pyle, A; Sewry, C; Pollitt, C; Johnson, MA; Davison, K; Moss, JA; Mercuri, E; Muntoni, F; Bushby, KMD
      Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies

      NEUROMUSCULAR DISORDERS
    28. Venken, K; Meuleman, J; Irobi, J; Ceuterick, C; Martini, R; De Jonghe, P; Timmerman, V
      CasprI/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies

      NEUROREPORT
    29. Chung, MY; Lu, JH; Weng, YY; Hwang, BT
      Absence of mutations in human ubiquitin fusion-degradation protein gene intetralogy of Fallot

      JOURNAL OF MOLECULAR MEDICINE-JMM
    30. Ning, CC; Chao, SC; Uitto, J; Shieh, CC; Lee, JYY
      Mutation analysis in the family of a Taiwanese boy with with epidermolysisbullosa simplex Dowling-Meara

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    31. Moraitou, M; van Weely, S; Verhoek, M; Aerts, J; Dimitriou, E; Michelakakis, H
      The facile detection of 1505G -> A in Gaucher patients with different phenotypes

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    32. Vergilio, SR; Maldonado, JC; Jino, M
      Constraint based criteria: An approach for test case selection in the structural testing

      JOURNAL OF ELECTRONIC TESTING-THEORY AND APPLICATIONS
    33. Becker, K; Csikos, M; Horvath, A; Karpati, S
      Identification of a novel mutation in 3 beta-hydroxysteroid-Delta 8-Delta 7-isomerase in a case of Conradi-Hunermann-Happle syndrome

      EXPERIMENTAL DERMATOLOGY
    34. Watzinger, F; Mayr, B; Gamerith, R; Vetter, C; Lion, T
      Comparative analysis of ras proto-oncogene mutations in selected mammaliantumors

      MOLECULAR CARCINOGENESIS
    35. Chen, T; Mittelstaedt, RA; Aidoo, A; Hamilton, LP; Beland, FA; Casciano, DA; Heflich, RH
      Comparison of hprt and lacl mutant frequency with DNA adduct formation in N-hydroxy-2-acetylaminoflourene-treated Big Blue((R)) rats

      ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
    36. Depowski, PL; Rosenthal, SI; Ross, JS
      Loss of expression of the PTEN gene protein product is associated with poor outcome in breast cancer

      MODERN PATHOLOGY
    37. Romano, V; Lio, D; Cali, F; Scola, L; Leggio, L; D'Anna, C; De Leo, G; Salerno, A
      A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia

      MOLECULAR AND CELLULAR PROBES
    38. Ayres, JA; Shum, L; Akarsu, AN; Dashner, R; Takahashi, K; Ikura, T; Slavkin, HC; Nuckolls, GH
      DACH: Genomic characterization, evaluation as a candidate for postaxial polydactyly type A2, and developmental expression pattern of the mouse homologue

      GENOMICS
    39. Cunliffe, P; Reed, V; Boyd, Y
      Intragenic deletions at Atp7a in mouse models for Menkes disease

      GENOMICS
    40. Pal, T; Liede, A; Mitchell, M; Calender, A; Narod, SA
      Intestinal carcinoid tumours in a father and daughter

      CANADIAN JOURNAL OF GASTROENTEROLOGY
    41. Paakkonen, K; Sauramo, S; Sarantaus, L; Vahteristo, P; Hartikainen, A; Vehmanen, P; Ignatius, J; Ollikainen, V; Kaariainen, H; Vauramo, E; Nevanlinna, H; Krahe, R; Holli, K; Kere, J
      Involvement of BRCA1 and BRCA2 in breast cancer in a Western Finnish sub-population

      GENETIC EPIDEMIOLOGY
    42. Calender, A; Cadiot, G; Mignon, M
      Multiple endocrine neoplasia type 1: genetic and clinical aspects

      GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE
    43. Hanke, S; Bugert, P; Chudek, J; Kovacs, G
      Cloning a calcium channel alpha 2 delta-3 subunit gene from a putative tumor suppressor gene region at chromosome 3p21.1 in conventional renal cell carcinoma

      GENE
    44. Waye, JS; Eng, B; Patterson, M; Walker, L; Carcao, MD; Olivieri, NF; Chui, DHK
      Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases

      AMERICAN JOURNAL OF HEMATOLOGY
    45. Dudesek, A; Roschinger, W; Muntau, AC; Seidel, J; Leupold, D; Thony, B; Blau, N
      Molecular analysis and long-term follow-up of patients with different forms of 6-pyruvoyl-tetrahydropterin synthase deficiency

      EUROPEAN JOURNAL OF PEDIATRICS
    46. Schmitt, LM
      Theory of genetic algorithms

      THEORETICAL COMPUTER SCIENCE
    47. Chandrasekharappa, SC; Teh, BT
      Clinical and molecular aspects of multiple endocrine neoplasia type 1

      GENETIC DISORDERS OF ENDOCRINE NEOPLASIA
    48. Sobottka, SB; Huebner, A; Haase, M; Ahrens, W; Rupprecht, E; Schackert, HK; Schackert, G
      Albright's hereditary osteodystrophy associated with cerebellar pilocytic astrocytoma: Coincidence or genetic relationship?

      HORMONE RESEARCH
    49. Kibel, AS; Christopher, M; Faith, DA; Bova, GS; Goodfellow, PJ; Isaacs, WB
      Methylation and mutational analysis of p27(kipl) in prostate carcinoma

      PROSTATE
    50. Benit, P; Bonnefont, JP; Mostefa, AK; Francannet, C; Munnich, A; Ray, PF
      Denaturing high-performance liquid chromatography (DHPLC)-based prenatal diagnosis for tuberous sclerosis

      PRENATAL DIAGNOSIS
    51. Kleijer, WJ; van Diggelen, OP; Keulemans, JLM; Losekoot, M; Garritsen, VH; Stroink, H; Majoor-Krakauer, D; Franken, PF; Eurlings, MCM; Taschner, PEM; Los, FJ; Galjaard, RJH
      First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis(LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis

      PRENATAL DIAGNOSIS
    52. Jonas, L; Fulda, G; Salameh, T; Schmidt, W; Kroning, GE; Hopt, UT; Nizze, H
      Electron microscopic detection of copper in the liver of two patients withmorbus Wilson by EELS and EDX

      ULTRASTRUCTURAL PATHOLOGY
    53. Giedraitis, V; He, B; Huang, WX; Hillert, J
      Cloning and mutation analysis of the human IL-18 promoter: a possible roleof polymorphisms in expression regulation

      JOURNAL OF NEUROIMMUNOLOGY
    54. Holinski-Feder, E; Muller-Koch, Y; Friedl, W; Moselein, G; Keller, G; Plaschke, J; Ballhausen, W; Gross, M; Baldwin-Jedele, K; Jungck, M; Mangold, E; Vogelsang, H; Schackert, HK; Lohse, P; Murken, J; Meitinger, T
      DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    55. Oldenburg, J; Ivaskevicius, V; Rost, S; Fregin, A; White, K; Holinski-Feder, E; Muller, CR; Weber, BHF
      Evaluation of DHPLC in the analysis of hemophilia A

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    56. Cooper, SC; Flaitz, CM; Johnston, DA; Lee, B; Hecht, JT
      A natural history of cleidocranial dysplasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    57. Arango, D; Cruts, M; Torres, O; Backhovens, H; Serrano, ML; Villareal, E; Montanes, P; Matallana, D; Cano, C; Van Broeckhoven, C; Jacquier, M
      Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    58. Verloes, A; Dresse, MF; Keutgen, H; Asplund, C; Smith, CIE
      Microphthalmia, facial anomalies, microcephaly, thumb and hallux hypoplasia, and agammaglobulinemia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    59. El-Naggar, AK; Lai, SL; Clayman, GL; Mims, B; Lippman, SM; Coombes, M; Luna, MA; Lozano, G
      p73 gene alterations and expression in primary oral and laryngeal squamouscarcinomas

      CARCINOGENESIS
    60. Delamaro, ME; Maldonado, JC; Mathur, AP
      Interface mutation: An approach for integration testing

      IEEE TRANSACTIONS ON SOFTWARE ENGINEERING
    61. Shulman, LP; Elias, S
      Cystic fibrosis

      CLINICS IN PERINATOLOGY
    62. Baldus, SE; Schneider, PM; Monig, SP; Zirbes, TK; Fromm, S; Meyer, W; Glossmann, J; Schuler, S; Thiele, J; Holscher, AH; Dienes, HP
      p21/waf1/cip1 In gastric cancer: Associations with histopathological subtypes, lymphonodal metastasis, prognosis and p53 status

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    63. Heil, SG; Levtchenko, E; Monnens, LAH; Trijbels, FJM; Van der Put, NMJ; Blom, HJ
      The molecular basis of Dutch infantile nephropathic cystinosis

      NEPHRON
    64. van Tilborg, AAG; de Vries, A; Zwarthoff, EC
      The chromosome 9q genes TGFBR1, TSC1, and ZNF189 are rarely mutated in bladder cancer

      JOURNAL OF PATHOLOGY
    65. Nagata, T; Werner, MH
      Functional mutagenesis of AML1/RUNX1 and PEBP2 beta/CBF beta define distinct, non-overlapping sites for DNA recognition and heterodimerization by theRunt domain

      JOURNAL OF MOLECULAR BIOLOGY
    66. Greber-Platzer, S; Marx, M; Fleischmann, C; Suppan, C; Dobner, M; Wimmer, M
      Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children

      JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
    67. Mura, C; Le Gac, G; Scotet, V; Raguenes, O; Mercier, AY; Ferec, C
      Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs

      JOURNAL OF MEDICAL GENETICS
    68. Francannet, C; Cohen-Tanugi, A; Le Merrer, M; Munnich, A; Bonaventure, J; Legeai-Mallet, L
      Genotype-phenotype correlation in hereditary multiple exostoses

      JOURNAL OF MEDICAL GENETICS
    69. Muroya, K; Hasegawa, T; Ito, Y; Nagai, T; Isotani, H; Iwata, Y; Yamamoto, K; Fujimoto, S; Seishu, S; Fukushima, Y; Hasegawa, Y; Ogata, T
      GATA3 abnormalities and the phenotypic spectrum of HDR syndrome

      JOURNAL OF MEDICAL GENETICS
    70. Caffarri, S; Croce, R; Breton, J; Bassi, R
      The major antenna complex of photosystem II has a xanthophyll binding sitenot involved in light harvesting

      JOURNAL OF BIOLOGICAL CHEMISTRY
    71. Honsho, M; Fujiki, Y
      Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments - Study using human membrane protein PMP34

      JOURNAL OF BIOLOGICAL CHEMISTRY
    72. Van Leuven, F; Thiry, E; Lambrechts, M; Stas, L; Boon, T; Bruynseels, K; Muls, E; Descamps, O
      Sequencing of the coding exons of the LRP1 and LDLR genes on individual DNA samples reveals novel mutations in both genes

      ATHEROSCLEROSIS
    73. Vaarala, MH; Porvari, K; Kyllonen, A; Lukkarinen, O; Vihko, P
      The TMPRSS2 gene encoding transmembrane serine protease is overexpressed in a majority of prostate cancer patients: Detection of mutated TMPRSS2 formin a case of aggressive disease

      INTERNATIONAL JOURNAL OF CANCER
    74. Omholt, K; Platz, A; Ringborg, U; Hansson, J
      Cytoplasmic and nuclear accumulation of beta-catenin is rarely caused by CTNNB1 exon 3 mutations in cutaneous malignant melanoma

      INTERNATIONAL JOURNAL OF CANCER
    75. Gimm, O; Dziema, H; Brown, J; De la Puente, A; Hoang-Vu, C; Dralle, H; Plass, C; Eng, C
      Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants

      INTERNATIONAL JOURNAL OF CANCER
    76. Lamszus, K; Lachenmayer, L; Heinemann, U; Kluwe, L; Finckh, U; Hoppner, W; Stavrou, D; Fillbrandt, R; Westphal, M
      Molecular genetic alterations on chromosomes 11 and 22 in ependymomas

      INTERNATIONAL JOURNAL OF CANCER
    77. Cederquist, K; Golovleva, I; Emanuelsson, M; Stenling, R; Gronberg, H
      A population based cohort study of patients with multiple colon and endometrial cancer: Correlation of microsatellite instability (MSI) status, age at diagnosis and cancer risk

      INTERNATIONAL JOURNAL OF CANCER
    78. Pereira, AC; Mota, GFA; Krieger, JE
      Hemochromatosis gene variants in three different ethnic populations: Effects of admixture for screening programs

      HUMAN BIOLOGY
    79. Gath, R; Goessling, A; Keller, KM; Koletzko, S; Coerdt, W; Muntefering, H; Wirth, S; Hofstra, RMW; Mulligan, L; Eng, C; von Deimling, A
      Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease

      GUT
    80. Huang, S; Lichtenauer, UD; Pack, S; Wang, C; Kim, AC; Lutchman, M; Koch, CA; Torres-Cruz, J; Huang, SC; Benz, EJ; Christiansen, H; Dockhorn-Dworniczak, B; Poremba, C; Vortmeyer, AO; Chishti, AH; Zhuang, Z
      Reassignment of the EPB4 center dot 1 gene to 1p36 and assessment of its involvement in neuroblastomas

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    81. Nowaczyk, MJM; Waye, JS
      The Smith-Lemli-Opitz syndrome: a novel metabolic way of understanding developmental biology, embryogenesis, and dysmorphology

      CLINICAL GENETICS
    82. Le Gac, G; Mura, C; Ferec, C
      Complete scanning of the hereditary hemochromatosis gene (HFE) by use of denaturing HPLC

      CLINICAL CHEMISTRY
    83. Lyon, E; Frank, EL
      Hereditary hemochromatosis since discovery of the HFE gene

      CLINICAL CHEMISTRY
    84. Roe, DS; Vianey-Saban, C; Sharma, S; Zabot, MT; Roe, CR
      Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

      CLINICA CHIMICA ACTA
    85. Gorgoulis, VG; Zacharatos, P; Mariatos, G; Liloglou, T; Kokotas, S; Kastrinakis, N; Kotsinas, A; Athanasiou, A; Foukas, P; Zoumpourlis, V; Kletsas, D; Ikonomopoulos, J; Asimacopoulos, PJ; Kittas, C; Field, JK
      Deregulated expression of c-mos in non-small cell lung carcinomas: Relationship with p53 status, genomic instability, and tumor kinetics

      CANCER RESEARCH
    86. Hough, CD; Cho, KR; Zonderman, AB; Schwartz, DR; Morin, PJ
      Coordinately up-regulated genes in ovarian cancer

      CANCER RESEARCH
    87. Chin, SF; Wang, Q; Puisieux, A; Caldas, C
      Absence of rearrangements in the BRCA2 gene in human cancers

      BRITISH JOURNAL OF CANCER
    88. Conconi, A; Bertoni, F; Pedrinis, E; Motta, T; Roggero, E; Luminari, S; Capella, C; Bonato, M; Cavalli, F; Zucca, E
      Nodal marginal zone B-cell lymphomas may arise from different subsets of marginal zone B lymphocytes

      BLOOD
    89. Croce, R; Muller, MG; Bassi, R; Holzwarth, AR
      Carotenoid-to-chlorophyll energy transfer in recombinant major light-harvesting complex (LHCII) of higher plants. I. Femtosecond transient absorptionmeasurements

      BIOPHYSICAL JOURNAL
    90. Moya, I; Silvestri, M; Vallon, O; Cinque, G; Bassi, R
      Time-resolved fluorescence analysis of the photosystem II antenna proteinsin detergent micelles and liposomes

      BIOCHEMISTRY
    91. Belosludtsev, Y; Belosludtsev, I; Iverson, B; Lemeshko, S; Wiese, R; Hogan, M; Powdrill, T
      Nearly instantaneous, cation-independent, high selectivity nucleic acid hybridization to DNA microarrays

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    92. Crockett, AO; Wittwer, CT
      Fluorescein-labeled oligonucleotides for real-time PCR: Using the inherentquenching of deoxyguanosine nucleotides

      ANALYTICAL BIOCHEMISTRY
    93. Mutter, GL
      Commentary - PTEN, a protean tumor suppressor

      AMERICAN JOURNAL OF PATHOLOGY
    94. Pereira, AC; Cuoco, MAR; Mota, GF; da Silva, FF; Freitas, HFG; Bocchi, EA; Soler, JMP; Mansur, AJ; Krieger, JE
      Hemochromatosis gene variants in patients with cardiomyopathy

      AMERICAN JOURNAL OF CARDIOLOGY
    95. Bulus, NM; Sheng, HM; Sizemore, N; Oldham, SM; Barnett, JV; Coffey, RJ; Beauchamp, DR; Barnard, JA
      Ras-mediated suppression of TGF beta RII expression in intestinal epithelial cells involves Raf-independent signaling

      NEOPLASIA
    96. Niemela, JE; Puck, JM; Fischer, RE; Fleisher, TA; Hsu, AP
      Efficient detection of thirty-seven new IL2RG mutations in human X-linked severe combined immunodeficiency

      CLINICAL IMMUNOLOGY
    97. Mella, P; Imberti, L; Brugnoni, D; Pirovano, S; Candotti, F; Mazzolari, E; Bettinardi, A; Fiorini, M; De Mattia, D; Martire, B; Plebani, A; Notarangelo, LD; Giliani, S
      Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: Molecular and cellular characterization

      CLINICAL IMMUNOLOGY
    98. Yalcinkaya, F; Tekin, M; Cakar, N; Akar, E; Akar, N; Tumer, N
      Familial Mediterranean fever and systemic amyloidosis in untreated Turkishpatients

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    99. Lee, CC; Wu, JY; Tsai, FJ; Kodama, H; Abe, T; Yang, CF; Tsai, CH
      Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association

      JOURNAL OF HUMAN GENETICS
    100. Sommer, N; Salniene, V; Gineikiene, E; Nivinskas, R; Ruger, W
      T4 early promoter strength probed in vivo with unribosylated and ADP-ribosylated Escherichia coli RNA polymerase: a mutation analysis

      MICROBIOLOGY-UK


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Documento generato il 06/08/20 alle ore 16:48:18