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    1. Aldape, K; Ginzinger, DG; Godfrey, TE
      Real-time quantitative polymerase chain reaction: A potential tool for genetic analysis in neuropathology

      BRAIN PATHOLOGY
    2. Konig, EA; Koves, I; Rasinariu, A; Popp, AR; Kusser, WC; Soyonki, K; Kovacs, A; Glickman, BW; Jeney, A; Marcsek, ZL
      Alterations of K-ras and p53 mutations in colorectal cancer patients in Central Europe

      JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
    3. Vais, H; Williamson, MS; Devonshire, AL; Usherwood, PNR
      The molecular interactions of pyrethroid insecticides with insect and mammalian sodium channels

      PEST MANAGEMENT SCIENCE
    4. Deeks, SG
      Nonnucleoside reverse transcriptase inhibitor resistance

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    5. Carlton, JMR; Hayton, M; Cravo, PVL; Walliker, D
      Of mice and malaria mutants: unravelling the genetics of drug resistance using rodent malaria models

      TRENDS IN PARASITOLOGY
    6. Syvanen, AC
      Accessing genetic variation: Genotyping single nucleotide polymorphisms

      NATURE REVIEWS GENETICS
    7. Ma, LL; Yamada, S; Wirtz, D; Coulombe, PA
      A 'hot-spot' mutation alters the mechanical properties of keratin filamentnetworks

      NATURE CELL BIOLOGY
    8. Campos, B; Diez, O; Cortes, J; Domenech, M; Pericay, C; Alonso, C; Baiget, M
      Conditions for single-strand conformation polymorphism (SSCP) analysis of BRCA1 gene using an automated electrophoresis unit

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    9. Lalouel, JM; Rohrwasser, A
      Development of genetic hypotheses in essential hypertension

      JOURNAL OF HUMAN GENETICS
    10. Abdel-Malek, ZA
      Melanocortin receptors: their functions and regulation by physiological agonists and antagonists

      CELLULAR AND MOLECULAR LIFE SCIENCES
    11. 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
    12. Bianchi, NO; Bianchi, MS; Richard, SM
      Mitochondrial genome instability in human cancers

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    13. McKenzie, GJ; Rosenberg, SM
      Adaptive mutations, mutator DNA polymerases and genetic change strategies of pathogens

      CURRENT OPINION IN MICROBIOLOGY
    14. Megraud, F
      Resistance of Helicobacter pylori to antibiotics and its impact on treatment options

      DRUG RESISTANCE UPDATES
    15. Carlson, CS; Newman, TL; Nickerson, DA
      SNPing in the human genome

      CURRENT OPINION IN CHEMICAL BIOLOGY
    16. Houlston, RS
      What we could do now: molecular pathology of colorectal cancer

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    17. Eberl, KJ; Jelinek, T; Aida, AO; Peyerl-Hoffmann, G; Heuschkel, C; el Valy, AO; Christophel, EM
      Prevalence of polymorphisms in the dihydrofolate reductase and dihydropteroate synthetase genes of Plasmodium falciparum isolates from southern Mauritania

      TROPICAL MEDICINE & INTERNATIONAL HEALTH
    18. Kijak, GH; Pampuro, SE; Avila, MM; Zala, C; Cahn, P; Wainberg, MA; Salomon, H
      Resistance profiles to antiretroviral drugs in HIV-1 drug-naive patients in Argentina

      ANTIVIRAL THERAPY
    19. Kato, T
      The other, forgotten genome: mitochondrial DNA and mental disorders

      MOLECULAR PSYCHIATRY
    20. Zayas-Rivera, B; Zhang, LF; Grant, SG; Keohavong, P; Day, BW
      Mutational spectrum of N-hydroxy-N-acetyl-4-aminobiphenyl at exon 3 of theHPRT gene

      BIOMARKERS
    21. Palau, F
      Friedreich's ataxia and frataxin: Molecular genetics, evolution and pathogenesis (Review)

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    22. Horenstein, J; Wagner, DA; Czajkowski, C; Akabas, MH
      Protein mobility and GABA-induced conformational changes in GABA(A) receptor pore-lining M2 segment

      NATURE NEUROSCIENCE
    23. Gomez-Zaera, M; Strom, TM; Rodriguez, B; Estivill, X; Meitinger, T; Nunes, V
      Presence of a major WFS1 mutation in Spanish wolfram syndrome pedigrees

      MOLECULAR GENETICS AND METABOLISM
    24. Medvedovic, M; Succop, P; Shukla, R; Dixon, K
      Clustering mutational spectra via classification likelihood and Markov chain Monte Carlo algorithms

      JOURNAL OF AGRICULTURAL BIOLOGICAL AND ENVIRONMENTAL STATISTICS
    25. Issaq, HJ; Xu, HY; Chan, KC
      A study of parameters that influence the HPLC and CE separation of double stranded DNA fragments and DNA mutants

      JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
    26. Heyworth, PG; Curnutte, JT; Rae, J; Noack, D; Roos, D; van Koppen, E; Cross, AR
      Hematologically important mutations: X-linked chronic granulomatous disease (Second update)

      BLOOD CELLS MOLECULES AND DISEASES
    27. 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
    28. Brega, A; Narula, J; Arbustini, E
      Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases

      JOURNAL OF NUCLEAR CARDIOLOGY
    29. Etoh, T; Ueo, H; Inoue, H; Sato, K; Utsunomiya, T; Barnard, GF; Kitano, S; Mori, M
      Clinical significance of K-ras mutations in intraoperative tumor drainage blood from patients with colorectal carcinoma

      ANNALS OF SURGICAL ONCOLOGY
    30. He, X; Zhu, DL; Chu, SL; Jin, L; Xiong, MM; Wang, GL; Zhang, WZ; Zhou, HF; Mao, SY; Zhan, YM; Zhuang, QN; Liu, XM; Zhao, Y; Huang, W
      alpha-adducin gene and essential hypertension in China

      CLINICAL AND EXPERIMENTAL HYPERTENSION
    31. Coller, HA; Khrapko, K; Bodyak, ND; Nekhaeva, E; Herrero-Jimenez, P; Thilly, WG
      High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection

      NATURE GENETICS
    32. Harnevik, L; Fjellstedt, E; Molbaek, A; Tiselius, HG; Denneberg, T; Soderkvist, P
      Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients

      HUMAN MUTATION
    33. Wong, LJC; Wang, JJ; Zhang, YH; Hsu, E; Heim, RA; Bowman, CM; Woo, MS
      Improved detection of CFTR mutations in southern California Hispanic CF patients

      HUMAN MUTATION
    34. Goldrick, MM
      RNase cleavage-based methods for mutation/SNP detection, past and present

      HUMAN MUTATION
    35. Bezieau, S; Devilder, MC; Avet-Loiseau, H; Mellerin, MP; Puthier, D; Pennarun, E; Rapp, MJ; Harousseau, JL; Moisan, JP; Bataille, R
      High incidence of N and K-Ras activating mutations in multiple myeloma andprimary plasma cell leukemia at diagnosis

      HUMAN MUTATION
    36. Gut, IG
      Automation in genotyping of single nucleotide polymorphisms

      HUMAN MUTATION
    37. Busson-Le Coniat, M; Khac, FN; Daniel, MT; Bernard, OA; Berger, R
      Chromosome 21 abnormalities with AMLI amplification in acute lymphoblasticleukemia

      GENES CHROMOSOMES & CANCER
    38. Clementino, NCD; Yamamoto, M; Viana, MB; Figueiredo, MS; Kerbauy, J; Saad, STO; Costa, FF
      Lack of association between N-ras gene mutations and clinical prognosis inBrazilian children with acute lymphoblastic leukemia

      LEUKEMIA & LYMPHOMA
    39. Palmgren, MG
      Plant plasma membrane H+-ATPases: Powerhouses for nutrient uptake

      ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
    40. Ozawa, E; Nishino, I; Nonaka, I
      Sarcolemmopathy: Muscular dystrophies with cell membrane defects

      BRAIN PATHOLOGY
    41. Shumaker, JM; Tollet, JJ; Filbin, KJ; Montague-Smith, MP; Pirrung, MC
      APEX disease gene resequencing: Mutations in exon 7 of the p53 tumor suppressor gene

      BIOORGANIC & MEDICINAL CHEMISTRY
    42. Lee, SH; Soderlund, DM
      The V410M mutation associated with pyrethroid resistance in Heliothis virescens reduces the pyrethroid sensitivity of house fly sodium channels expressed in Xenopus oocytes

      INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
    43. Cairo, S; Merla, G; Urbinati, F; Ballabio, A; Reymond, A
      WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, isa new member of the Mlx transcription factor network

      HUMAN MOLECULAR GENETICS
    44. Fletcher, S; Ly, T; Duff, RM; Howell, JM; Wilton, SD
      Cryptic splicing involving the splice site mutation in the canine model ofDuchenne muscular dystrophy

      NEUROMUSCULAR DISORDERS
    45. Otani, K; Shimizu, S; Chijiiwa, K; Yamaguchi, K; Noshiro, H; Tanaka, M
      Immunohistochemical detection of 8-hydroxy-2 '-deoxyguanosine in gallbladder epithelium of patients with pancreaticobiliary maljunction

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    46. O'Mahony, S; Sreedharan, A
      Does detection of K-ras mutations in pancreatic juice influence clinical decision making?

      EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
    47. Duplessis, M; Moineau, S
      Identification of a genetic determinant responsible for host specificity in Streptococcus thermophilus bacteriophages

      MOLECULAR MICROBIOLOGY
    48. Volkmann, M; Schiff, JH; Hajjar, Y; Otto, G; Stilgenbauer, F; Fiehn, W; Galle, PR; Hofmann, WJ
      Loss of CD95 expression is linked to most but not all p53 mutants in European hepatocellular carcinoma

      JOURNAL OF MOLECULAR MEDICINE-JMM
    49. Trulzsch, B; Krohn, K; Wonerow, P; Chey, S; Holzapfel, HP; Ackermann, F; Fuhrer, D; Paschke, R
      Detection of thyroid-stimulating hormone receptor and G(s)alpha mutations:in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis

      JOURNAL OF MOLECULAR MEDICINE-JMM
    50. Dzierzanowska-Fangrat, K; Rozynek, E; Jozwiak, P; Celinska-Cedro, D; Madalinski, K; Dzierzanowska, D
      Primary resistance to clarithromycin in clinical strains of Helicobacter pylori isolated from children in Poland

      INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
    51. Takano, T; Miyauchi, A; Yoshida, H; Hasegawa, Y; Kuma, K; Amino, N
      Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan

      JAPANESE JOURNAL OF CANCER RESEARCH
    52. Hunger, RE; Brand, CU; Streit, M; Eriksen, JA; Gjertsen, MK; Saeterdal, I; Braathen, LR; Gaudernack, G
      Successful induction of immune responses against mutant ras in melanoma patients using intradermal injection of peptides and GM-CSF as adjuvant

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

      MOLECULAR CARCINOGENESIS
    54. 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
    55. King, NM; Oakley, GG; Medvedovic, M; Dixon, K
      XPA protein alters the specificity of ultraviolet light-induced mutagenesis in vitro

      ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
    56. Pesce, V; Cormio, A; Fracasso, F; Vecchiet, J; Felzani, G; Lezza, AMS; Cantatore, P; Gadaleta, MN
      Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle

      FREE RADICAL BIOLOGY AND MEDICINE
    57. Yang, YJ; Yang, JC; Jeng, YM; Chang, MH; Ni, YH
      Prevalence and rapid identification of clarithromycin-resistant Helicobacter pylori isolates in children

      PEDIATRIC INFECTIOUS DISEASE JOURNAL
    58. Hatzaki, A; Razi, E; Anagnostopoulou, K; Iliadis, K; Kodaxis, A; Papaioannou, D; Labropoulos, S; Vasilaki, M; Kosmidis, P; Saetta, A; Mihalatos, M; Nasioulas, G
      A modified mutagenic PCR-RFLP method for K-ras codon 12 and 13 mutations detection in NSCLC patients

      MOLECULAR AND CELLULAR PROBES
    59. 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
    60. Simon, DK; Lin, MT; Ahn, CH; Liu, GJ; Gibson, GE; Beal, MF; Johns, DR
      Low mutational burden of individual acquired mitochondrial DNA mutations in brain

      GENOMICS
    61. Steer, EJ; Goldman, JM; Cross, NCP
      Mutations of the transcription factor AML1/CBFA2 are uncommon in blastic transformation of chronic myeloid leukaemia

      LEUKEMIA
    62. Villoutreix, BO; Dahlback, B; Borgel, D; Gandrille, S; Muller, YA
      Three-dimensional model of the SHBG-like region of anticoagulant protein S: New structure-function insights

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    63. Ha, A; Watanabe, H; Yamaguchi, Y; Ohtsubo, K; Wang, Y; Motoo, Y; Okai, T; Wakabayahi, T; Sawabu, N
      Usefulness of supernatant of pancreatic juice for genetic analysis of K-ras in diagnosis of pancreatic carcinoma

      PANCREAS
    64. Katti, MV; Ranjekar, PK; Gupta, VS
      Differential distribution of simple sequence repeats in eukaryotic genome sequences

      MOLECULAR BIOLOGY AND EVOLUTION
    65. Noor, MAF; Kliman, RM; Machado, CA
      Evolutionary history of microsatellites in the obscure group of Drosophila

      MOLECULAR BIOLOGY AND EVOLUTION
    66. Sibly, RM; Whittaker, JC; Talbot, M
      A maximum-likelihood approach to fitting equilibrium models of microsatellite evolution

      MOLECULAR BIOLOGY AND EVOLUTION
    67. Kristensen, VN; Kelefiotis, D; Kristensen, T; Borresen-Dale, AL
      High-throughput methods for detection of genetic variation

      BIOTECHNIQUES
    68. Kapila, Y; Doan, D; Tafolla, E; Fletterick, R
      Three-dimensional structural analysis of fibronectin heparin-binding domain mutations

      JOURNAL OF CELLULAR BIOCHEMISTRY
    69. Incorvaia, C; Parmeggiani, F; Costagliola, C; Lamberti, G; Ferraresi, P; Bernardi, F; Sebastiani, A
      The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    70. Van Remmen, H; Richardson, A
      Oxidative damage to mitochondria and aging

      EXPERIMENTAL GERONTOLOGY
    71. Speletas, M; Arvanitidis, K; Tzoanopoulos, D; Tsironidou, V; Pardali, E; Aggeli, C; Tsapogas, P; Kartalis, G; Sideras, P; Ritis, K
      Rapid mutational analysis of N-ras proto-oncogene in hematologic malignancies: a study of 77 Greek patients

      HAEMATOLOGICA
    72. Pietrapertosa, A; Palma, A; Campanale, D; Delios, G; Vitucci, A; Tannoia, N
      Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency

      HAEMATOLOGICA
    73. Inoue, K; Tanaka, H; Scaglia, F; Araki, A; Shaffer, LG; Lupski, JR
      Compensating for central nervous system dysmyelination: Females with a proteolipid protein gene duplication and sustained clinical improvement

      ANNALS OF NEUROLOGY
    74. Kerr, TP; Sewry, CA; Robb, SA; Roberts, RG
      Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?

      HUMAN GENETICS
    75. Simioni, P; Kalafatis, M; Tormene, D; Luni, S; Zerbinati, P; Barzon, L; Palu, G; Girolami, A
      Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma - Characterization of the dysfunctional protein C Padua(3) (Protein CR-1L/propeptide)

      THROMBOSIS AND HAEMOSTASIS
    76. Walsh, PN
      Roles of platelets and factor XI in the initiation of blood coagulation bythrombin

      THROMBOSIS AND HAEMOSTASIS
    77. Weihrauch, M; Benicke, M; Lehnert, G; Wittekind, C; Bader, M; Wrbitzky, R; Tannapfel, A
      High prevalence of K-ras-2 mutations in hepatocellular carcinomas in workers exposed to vinyl chloride

      INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH
    78. Benstead, TJ; Grant, IA
      Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    79. Noffsinger, AE; Belli, JM; Miller, MA; Fenoglio-Preiser, CM
      A unique basal pattern of p53 expression in ulcerative colitis is associated with mutation in the p53 gene

      HISTOPATHOLOGY
    80. Zhou, GH; Kamahori, M; Okano, K; Chuan, G; Harada, K; Kambara, H
      Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER)

      NUCLEIC ACIDS RESEARCH
    81. Kozlowski, P; Krzyzosiak, WJ
      Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection

      NUCLEIC ACIDS RESEARCH
    82. LaCount, DJ; El-Sayed, NM; Kaul, S; Wanless, D; Turner, CMR; Donelson, JE
      Analysis of a donor gene region for a variant surface glycoprotein and itsexpression site in African trypanosomes

      NUCLEIC ACIDS RESEARCH
    83. Ali, A; Randles, JW
      Genomic heterogeneity in Pea seed-borne mosaic virus isolates from Pakistan, the centre of diversity of the host species, Pisum sativum

      ARCHIVES OF VIROLOGY
    84. Pineda-Trujillo, NL; Carvajal-Carmona, LG; Buritica, O; Moreno, S; Uribe, C; Pineda, D; Toro, M; Garcia, F; Arias, W; Bedoya, G; Lopera, F; Ruiz-Lineares, A
      A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia

      NEUROSCIENCE LETTERS
    85. Desnick, RJ; Wasserstein, MP; Banikazemi, M
      Fabry disease (alpha-galactosidase A deficiency): Renal involvement and enzyme replacement therapy

      RARE KIDNEY DISEASES
    86. Germain, DP
      A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variant

      RARE KIDNEY DISEASES
    87. Schmiedel, J; Seibel, P; Reichmann, H
      Molecular biological diagnostics of metabolic myopathies

      AKTUELLE NEUROLOGIE
    88. Santos-Filho, OA; de Alencastro, RB; Figueroa-Villar, JD
      Homology modeling of wild type and pyrimethamine/cycloguanil-cross resistant mutant type Plasmodium falciparum dihydrofolate reductase. A model for antimalarial chemotherapy resistance

      BIOPHYSICAL CHEMISTRY
    89. Okamoto, Y; Tsuda, T; Matsunami, M; Hirose, T; Sakaguchi, R; Katayama, N; Ota, K
      Treatment of acute myeloblastic leukaemia in a patient with Bombay blood type: a case report

      JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
    90. Ko, HM; Chung, JH; Lee, JH; Jung, IS; Choi, IS; Juhng, SW; Choi, C
      Androgen receptor gene mutation associated with complete androgen insensitivity syndrome and Sertoli cell adenoma

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    91. Andersen, JN; Mortensen, OH; Peters, GH; Drake, PG; Iversen, LF; Olsen, OH; Jansen, PG; Andersen, HS; Tonks, NK; Moller, NPH
      Structural and evolutionary relationships among protein tyrosine phosphatase domains

      MOLECULAR AND CELLULAR BIOLOGY
    92. Lu, XD; Magrane, G; Yin, CY; Louis, DN; Gray, J; Van Dyke, T
      Selective inactivation of p53 facilitates mouse epithelial tumor progression without chromosomal instability

      MOLECULAR AND CELLULAR BIOLOGY
    93. Strutz, N; Villmann, C; Thalhammer, A; Kizelsztein, P; Eisenstein, M; Teichberg, VI; Hollmann, M
      Identification of domains and amino acids involved in GluR7 ion channel function

      JOURNAL OF NEUROSCIENCE
    94. Lewis, PD; Harvey, JS; Waters, EM; Skibinski, DOF; Parry, JM
      Spontaneous mutation spectra in supF: comparative analysis of mammalian cell line base substitution spectra

      MUTAGENESIS
    95. Meunier, B
      Site-directed mutations in the mitochondrially encoded subunits I and III of yeast cytochrome oxidase

      BIOCHEMICAL JOURNAL
    96. Sickmann, A; Marcus, K; Schafer, H; Butt-Dorje, E; Lehr, S; Herkner, A; Suer, S; Bahr, I; Meyer, HE
      Identification of post-translationally modified proteins in proteome studies

      ELECTROPHORESIS
    97. Kaczanowski, R; Trzeciak, L; Kucharczyk, K
      Multitemperature single-strand conformation polymorphism

      ELECTROPHORESIS
    98. Sperling, K
      From proteomics to genomics

      ELECTROPHORESIS
    99. Hara, H; Morita, S; Ishibashi, T; Sako, S; Dohi, T; Iwamoto, M; Tanigawa, N
      Surgical treatment for non-dilated biliary tract with pancreaticobiliary maljunction should include excision of the extrahepatic bile duct

      HEPATO-GASTROENTEROLOGY
    100. Hara, H; Morita, S; Ishibashi, T; Sako, S; Otani, M; Tanigawa, N
      Surgical treatment for congenital biliary dilatation, with or without intrahepatic bile duct dilatation

      HEPATO-GASTROENTEROLOGY


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Documento generato il 09/12/19 alle ore 14:37:51