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    1. Wess, J
      Considerations in the design and use of chimeric G protein-coupled receptors

      G PROTEIN PATHWAYS, PT A, RECEPTORS
    2. Nakamura, K; Ozaki, A; Akutsu, T; Iwai, K; Sakamoto, T; Yoshizaki, G; Okamoto, N
      Genetic mapping of the dominant albino locus in rainbow trout (Oncorhynchus mykiss)

      MOLECULAR GENETICS AND GENOMICS
    3. Panteleyev, AA; Christiano, AM
      The Charles River "hairless" rat mutation is distinct from the hairless mouse alleles

      COMPARATIVE MEDICINE
    4. Steinfeld, U; Sierotzki, H; Parisi, S; Poirey, S; Gisi, U
      Sensitivity of mitochondrial respiration to different inhibitors in Venturia inaequalis

      PEST MANAGEMENT SCIENCE
    5. Moriyama, K; Otsuka, C; Loakes, D; Negishi, K
      Highly efficient random mutagenesis in transcription-reversetranscription cycles by a hydrogen bond ambivalent nucleoside 5 '-triphosphate analogue: Potential candidates for a selective anti-retroviral therapy

      NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
    6. Mendoza, GJA; Seidel, NE; Otsu, M; Anderson, SM; Simon-Stoos, K; Herrera, A; Hoogstraten-Miller, S; Malech, HL; Candotti, F; Puck, JM; Bodine, DM
      Comparison of five retrovirus vectors containing the human IL-2 receptor gamma chain gene for their ability to restore T and B lymphocytes in the X-linked severe combined immunodeficiency mouse model

      MOLECULAR THERAPY
    7. Ballas, SK
      Effect of alpha-globin genotype on the pathophysiology of sickle cell disease

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    8. Fontenot, AP; Newman, LS; Kotzin, BL
      Chronic beryllium disease: T cell recognition of a metal presented by HLA-DP

      CLINICAL IMMUNOLOGY
    9. Drici, MD
      Influence of gender on drug-acquired long QT syndrome

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    10. Schulze-Bahr, E; Haverkamp, W; Eckardt, L; Kirchhof, P; Wedekind, H; Breithardt, G
      Genetic aspects in acquired long QT syndrome - a piece in the puzzle

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    11. Doyle, HA; Mamula, MJ
      Post-translational protein modifications in antigen recognition and autoimmunity

      TRENDS IN IMMUNOLOGY
    12. Weatherall, DJ
      Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias

      NATURE REVIEWS GENETICS
    13. Mackay, TFC
      Quantitative trait loci in Drosophila

      NATURE REVIEWS GENETICS
    14. Heintz, N
      Bac to the future: The use of bac transgenic mice for neuroscience research

      NATURE REVIEWS NEUROSCIENCE
    15. Audia, JP; Webb, CC; Foster, JW
      Breaking through the acid barrier: An orchestrated response to proton stress by enteric bacteria

      INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY
    16. Yamada, Y; Ichihara, S; Izawa, H; Tanaka, M; Yokota, M
      Association of a G(994) -> T (Val(279) -> Phe) polymorphism of the plasma platelet-activating factor acetylhydrolase gene with myocardial damage in Japanese patients with nonfamilial hypertrophic cardiomyopathy

      JOURNAL OF HUMAN GENETICS
    17. Han, HJ; Park, SH; Park, HJ; Lee, JH; Lee, BY; Hwang, WS
      Effects of sex hormones on Na+/glucose cotransporter of renal proximal tubular cells following oxidant injury

      KIDNEY & BLOOD PRESSURE RESEARCH
    18. Kumari, VK; Nagaraj, R
      Structure-function studies on the amphibian peptide brevinin 1E: translocating the cationic segment from the C-terminal end to a central position favors selective antibacterial activity

      JOURNAL OF PEPTIDE RESEARCH
    19. Montagna, P; Liguori, R; Monari, L; Strong, PN; Riva, R; Di Stasi, V; Gandini, G; Cipone, M
      Equine muscular dystrophy with myotonia

      CLINICAL NEUROPHYSIOLOGY
    20. Betzel, C
      X-ray structure analysis of food allergens

      JOURNAL OF CHROMATOGRAPHY B
    21. Pflegerl, K; Hahn, R; Schallaun, E; Josic, D; Jungbauer, A
      Quantification of plasma-derived blood coagulation factor VIII by real-time biosensor measurements

      JOURNAL OF CHROMATOGRAPHY B
    22. Suzuki, A; Maruno, A; Tahira, T; Hayashi, K
      Polar alteration of short tandem repeats (STRs) in mammalian cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    23. Marie, C; Broughton, WJ; Deakin, WJ
      Rhizobium type III secretion systems: legume charmers or alarmers?

      CURRENT OPINION IN PLANT BIOLOGY
    24. Caron, PR; Mullican, MD; Mashal, RD; Wilson, KP; Su, MS; Murcko, MA
      Chemogenomic approaches to drug discovery - Commentary

      CURRENT OPINION IN CHEMICAL BIOLOGY
    25. Kagoshima, M; Ito, T; Kitamura, H; Goshima, Y
      Diverse gene expression and function of semaphorins in developing lung: positive and negative regulatory roles of semaphorins in lung branching morphogenesis

      GENES TO CELLS
    26. Shirakabe, K; Terasawa, K; Miyama, K; Shibuya, H; Nishida, E
      Regulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5

      GENES TO CELLS
    27. Cangelosi, GA; Palermo, CO; Bermudez, LE
      Phenotypic consequences of red-white colony type variation in Mycobacterium avium

      MICROBIOLOGY-UK
    28. Cote, I; Rogers, NJ; Lechler, RI
      Allorecognition

      TRANSFUSION CLINIQUE ET BIOLOGIQUE
    29. Sandoe, JAT; Longshaw, CM
      Ventriculoperitoneal shunt infection caused by Staphylococcus lugdunensis

      CLINICAL MICROBIOLOGY AND INFECTION
    30. Sundberg, JP; King, LE
      Morphology of hair in normal and mutant laboratory mice

      EUROPEAN JOURNAL OF DERMATOLOGY
    31. Ma, SK; Au, WY; Chan, AYY; Chan, LC
      Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    32. Toth, T; Kupka, S; Esmer, H; Zeissler, U; Sziklai, I; Zenner, HP; Blin, N; Pfister, M
      Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    33. Malloy, PJ; Zhu, WJ; Zhao, XY; Pehling, GB; Feldman, D
      A novel inborn error in the ligand-binding domain of the vitamin D receptor causes hereditary vitamin D-resistant rickets

      MOLECULAR GENETICS AND METABOLISM
    34. Nakamura, K; Fukao, T; Perez-Cerda, C; Luque, C; Song, XQ; Naiki, Y; Kohno, Y; Ugarte, M; Kondo, N
      A novel single-base substitution (380C > T) that activates a 5-base downstream cryptic splice-acceptor site within exon 5 in almost all transcripts in the human mitochondrial acetoacetyl-CoA thiolase gene

      MOLECULAR GENETICS AND METABOLISM
    35. Leung, DW
      The structure and functions of human lysophosphatidic acid acyltransferases

      FRONTIERS IN BIOSCIENCE
    36. Gruel, N; Chapiro, J; Fridman, WH; Teillaud, JL
      Purification of soluble recombinant human Fc gamma RII (CD32)

      PREPARATIVE BIOCHEMISTRY & BIOTECHNOLOGY
    37. Fraunberg, MVZ; Tenhunen, R; Kauppinen, R
      Expression and characterization of six mutations in the protoporphyrinogenoxidase gene among Finnish variegate porphyria patients

      MOLECULAR MEDICINE
    38. Todd, JA; Wicker, LS
      Genetic protection from the inflammatory disease type 1 diabetes in humansand animal models

      IMMUNITY
    39. Helluin, O; Beyermann, M; Leuchtag, HR; Duclohier, H
      A critical role for the branched sidechain adjacent to the third arginine of the sodium channel voltage sensor

      IEEE TRANSACTIONS ON DIELECTRICS AND ELECTRICAL INSULATION
    40. Rando, TA
      Role of nitric oxide in the pathogenesis of muscular dystrophies: A "two hit" hypothesis, of the cause of muscle necrosis

      MICROSCOPY RESEARCH AND TECHNIQUE
    41. 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
    42. Firestein, BL; Rongo, C
      DLG-1 is a MAGUK similar to SAP97 and is required for adherens junction formation

      MOLECULAR BIOLOGY OF THE CELL
    43. de Silva, GDI; Justice, A; Wilkinson, AR; Buttery, J; Herbert, M; Day, NPJ; Peacock, SJ
      Genetic population structure of coagulase-negative staphylococci associated with carriage and disease in preterm infants

      CLINICAL INFECTIOUS DISEASES
    44. Ikehara, Y; Nishihara, S; Yasutomi, H; Kitamura, T; Matsuo, K; Shimizu, N; Inada, KI; Kodera, Y; Yamamura, Y; Narimatsu, H; Hamajima, N; Tatematsu, M
      Polymorphisms of two fucosyltransferase genes (Lewis and Secretor genes) involving type I Lewis antigens are associated with the presence of anti-Helicobacter pylori IgG antibody

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    45. Feldt-Rasmussen, U
      Iodine and Cancer

      THYROID
    46. Koibuchi, N; Yamaoka, S; Chin, WW
      Effect of altered thyroid status on neurotrophin gene expression during postnatal development of the mouse cerebellum

      THYROID
    47. Pond, AL; Nerbonne, JM
      ERG proteins and functional cardiac I-Kr channels in rat, mouse, and humanheart

      TRENDS IN CARDIOVASCULAR MEDICINE
    48. Schwartz, PJ
      Another role for the sympathetic nervous system in the long QT syndrome?

      JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
    49. Salonen, T; Heinonen-Kopra, O; Vesa, J; Jalanko, A
      Neuronal trafficking of palmitoyl protein thioesterase provides an excellent model to study the effects of different mutations which cause infantile neuronal ceroid lipofuscinocis

      MOLECULAR AND CELLULAR NEUROSCIENCE
    50. Dascal, N
      Ion-channel regulation by G proteins

      TRENDS IN ENDOCRINOLOGY AND METABOLISM
    51. Hoth, S; Geiger, D; Becker, D; Hedrich, R
      The pore of plant K+ channels is involved in voltage and pH sensing: Domain-swapping between different K+ channel alpha-subunits

      PLANT CELL
    52. Weerachatyanukul, W; Rattanachaiyanont, M; Carmona, E; Furimsky, A; Mai, A; Shoushtarian, A; Sirichotiyakul, S; Ballakier, H; Leader, A; Tanphaichitr, N
      Sulfogalactosylglycerolipid is involved in human gamete interaction

      MOLECULAR REPRODUCTION AND DEVELOPMENT
    53. Momynaliev, KT; Govorun, VM
      Mechanisms of genetic instability in mollicutes (mycoplasmas)

      RUSSIAN JOURNAL OF GENETICS
    54. Sokolova, O; Kolmakova-Partensky, L; Grigorieff, N
      Three-dimensional structure of a voltage-gated potassium channel at 2.5 nmresolution

      STRUCTURE
    55. Zekanowski, C; Nowacka, M; Radomyska, B; Cabalska, B
      Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience

      JOURNAL OF MEDICAL SCREENING
    56. Canto-Nogues, C; Hockley, D; Grief, C; Ranjbar, S; Bootman, J; Almond, N; Herrera, I
      Ultrastructural localization of the RNA of immunodeficiency viruses using electron microscopy in situ hybridization and in vitro infected lymphocytes

      MICRON
    57. Kosloff, M; Selinger, Z
      Substrate assisted catalysis application to G proteins

      TRENDS IN BIOCHEMICAL SCIENCES
    58. Winder, SJ
      The complexities of dystroglycan

      TRENDS IN BIOCHEMICAL SCIENCES
    59. Ogorelkova, M; Kraft, HG; Ehnholm, C; Utermann, G
      Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians

      HUMAN MOLECULAR GENETICS
    60. Khajavi, M; Tari, AM; Patel, NB; Tsuji, K; Siwak, DR; Meistrich, ML; Terry, NHA; Ashizawa, T
      'Mitotic drive' of expanded CTG repeats in myotonic dystrophy type 1 (DM1)

      HUMAN MOLECULAR GENETICS
    61. Cucca, F; Lampis, R; Congia, M; Angius, E; Nutland, S; Bain, SC; Barnett, AH; Todd, JA
      A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins

      HUMAN MOLECULAR GENETICS
    62. Das, AK; Lu, JY; Hofmann, SL
      Biochemical analysis of mutations in palmitoyl-protein thioesterase causing infantile and late-onset forms of neuronal ceroid lipofuscinosis

      HUMAN MOLECULAR GENETICS
    63. Peretz, D; Scott, MR; Groth, D; Williamson, RA; Burton, DR; Cohen, FE; Prusiner, SB
      Strain-specified relative conformational stability of the scrapie prion protein

      PROTEIN SCIENCE
    64. Jongsma, HJ; Wilders, R
      Channelopathies: Kir2.1 mutations jeopardize many cell functions

      CURRENT BIOLOGY
    65. George, AL; Bianchi, L; Link, EM; Vanoye, CG
      From stones to bones: The biology of CIC chloride channels

      CURRENT BIOLOGY
    66. Munro, S
      The MRH domain suggests a shared ancestry for the mannose 6-phosphate receptors and other N-glycan-recognising proteins

      CURRENT BIOLOGY
    67. Seefeld, MA; Miller, WH; Newlander, KA; Burgess, WJ; Payne, DJ; Rittenhouse, SF; Moore, TD; DeWolf, WE; Keller, PM; Qiu, XY; Janson, CA; Vaidya, K; Fosberry, AP; Smyth, MG; Jaworski, DD; Slater-Radosti, C; Huffman, WF
      Inhibitors of bacterial enoyl acyl carrier protein reductase (FabI): 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    68. Slack, JMW; Tosh, D
      Transdifferentiation and metaplasia - switching cell types

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    69. Goto, S; Tamura, N; Sakakibara, M; Ikeda, Y; Handa, S
      Effects of ticlopidine on von Willebrand factor-mediated shear-induced platelet activation and aggregation

      PLATELETS
    70. Maayani, S; Tagliente, TM; Schwarz, T; Martinelli, G; Martinez, R; Shore-Lesserson, L
      The balance of concurrent aggregation and deaggregation processes in platelets is linked to differential occupancy of ADP receptor subtypes

      PLATELETS
    71. Ma, JX; Kono, M; Lin, XU; Das, J; Ryan, JC; Hazard, ES; Oprian, DD; Crouch, RK
      Salamander UV cone pigment: Sequence, expression, and spectral properties

      VISUAL NEUROSCIENCE
    72. Clarke, P; Meintzer, SM; Spalding, AC; Johnson, GL; Tyler, KL
      Caspase 8-dependent sensitization of cancer cells to TRAIL-induced apoptosis following reovirus-infection

      ONCOGENE
    73. Fukuyama, T; Sueoka, E; Sugio, Y; Otsuka, T; Niho, Y; Akagi, K; Kozu, T
      MTG8 proto-oncoprotein interacts with the regulatory subunit of type II cyclic AMP-dependent protein kinase in lymphocytes

      ONCOGENE
    74. Saadi-Kheddouci, S; Berrebi, D; Romagnolo, B; Cluzeaud, F; Peuchmaur, M; Kahn, A; Vandewalle, A; Perret, C
      Early development of polycystic kidney disease in transgenic mice expressing an activated mutant of the beta-catenin gene

      ONCOGENE
    75. Koch, M; Hering, S; Barth, C; Ehren, M; Enderle, MD; Pfohl, M
      Paraoxonase 1 192 Gln/Arg gene polymorphism and cerebrovascular disease: interaction with type 2 diabetes

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    76. Leviev, N; Righetti, A; James, RW
      Paraoxonase promoter polymorphism T(-107)C and relative paraoxonase deficiency as determinants of risk of coronary artery disease

      JOURNAL OF MOLECULAR MEDICINE-JMM
    77. Lupoglazoff, JM; Denjoy, I; Guicheney, P; Casasoprana, A; Coumel, P
      Long QT syndrome.

      ARCHIVES DE PEDIATRIE
    78. Yang, HB; Sheu, BS; Chen, RC; Wu, JJ; Lin, XZ
      Erythrocyte Lewis antigen phenotypes of dyspeptic patients in Taiwan - Correlation of host factor with Helicobacter pylori infection

      JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION
    79. Shiran, B; Raina, SN
      Evidence of rapid evolution and incipient speciation in Vicia sativa species complex based on nuclear and organellar RFLPs and PCR analysis

      GENETIC RESOURCES AND CROP EVOLUTION
    80. Ryoo, YW; Kim, BC; Lee, KS
      Characterization of mutations of the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa mitis (M-RDEB) from three Korean patients

      JOURNAL OF DERMATOLOGICAL SCIENCE
    81. Katsuya, T; Iwashima, Y; Sugimoto, K; Motone, M; Asai, T; Fukuda, M; Fu, YX; Hatanaka, Y; Ohishi, M; Rakugi, H; Higaki, J; Ogihara, T
      Effects of antihypertensive drugs and gene variants in the renin-angiotensin system

      Hypertension research
    82. Laosombat, V; Wongchanchailert, M; Sattayasevana, B; Wiriyasateinkul, A; Fucharoen, S
      Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patients

      EUROPEAN JOURNAL OF HAEMATOLOGY
    83. Luyten, E; Swinnen, E; Vlassak, K; Verreth, C; Dombrecht, B; Vanderleyden, J
      Analysis of a symbiosis-specific cytochrome P450 homolog in Rhizobium sp, BR816

      MOLECULAR PLANT-MICROBE INTERACTIONS
    84. Ballvora, A; Pierre, M; van den Ackerveken, G; Schornack, S; Rossier, O; Ganal, M; Lahaye, T; Bonas, U
      Genetic mapping and functional analysis of the tomato Bs4 locus governing recognition of the Xanthomonas campestris pv. vesicatoria AvrBs4 protein

      MOLECULAR PLANT-MICROBE INTERACTIONS
    85. Lopez-Lara, IM; Geiger, O
      The nodulation protein NodG shows the enzymatic activity of an 3-oxoacyl-acyl carrier protein reductase

      MOLECULAR PLANT-MICROBE INTERACTIONS
    86. Lopez, JC; Grasso, DH; Frugier, F; Crespi, MD; Aguilar, OM
      Early symbiotic responses induced by Sinorhizobium meliloti ilvC mutants in alfalfa

      MOLECULAR PLANT-MICROBE INTERACTIONS
    87. Toyofuku, K; Wada, I; Valencia, JC; Kushimoto, T; Ferrans, VJ; Hearing, VJ
      Oculocutaneous albinism types 1 and 3 are ER retention diseases: mutation of tyrosinase or Tyrp1 can affect the processing of both mutant and wild-type proteins

      FASEB JOURNAL
    88. Sund, NJ; Vatamaniuk, MZ; Casey, M; Ang, SL; Magnuson, MA; Stoffers, DA; Matschinsky, FM; Kaestner, KH
      Tissue-specific deletion of Foxa2 in pancreatic beta cells results in hyperinsulinemic hypoglycemia

      GENES & DEVELOPMENT
    89. Pang, SY
      Congenital adrenal hyperplasia owing to 3 beta-hydroxysteroid dehydrogenase deficiency

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    90. Auchus, RJ
      The genetics, pathophysiology, and management of human deficiencies of P450c17

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    91. Ando, S; Sarlis, NJ; Krishnan, J; Feng, X; Refetoff, S; Zhang, MQ; Oldfield, EH; Yen, PM
      Aberrant alternative splicing of thyroid hormone receptor in a TSH-secreting pituitary tumor is a mechanism for hormone resistance

      MOLECULAR ENDOCRINOLOGY
    92. Cesario, RM; Klausing, K; Razzaghi, H; Crombie, D; Rungta, D; Heyman, RA; Lala, DS
      The rexinoid LG100754 is a novel RXR : PPAR gamma agonist and decreases glucose levels in vivo

      MOLECULAR ENDOCRINOLOGY
    93. Soejima, H; Kawamoto, S; Akai, J; Miyoshi, O; Arai, Y; Morohka, T; Matsuo, S; Niikawa, N; Kimura, A; Okubo, K; Mukai, T
      Isolation of novel heart-specific genes using the BodyMap database

      GENOMICS
    94. Lapidot, M; Pilpel, Y; Gilad, Y; Falcovitz, A; Sharon, D; Haaf, T; Lancet, D
      Mouse-human orthology relationships in an olfactory receptor gene cluster

      GENOMICS
    95. 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
    96. Martinez, M; Naranjo, T; Cuadrado, C; Romero, C
      The synaptic behaviour of the wild forms of Triticum turgidum and T-timopheevii

      GENOME
    97. Nagarajan, MM; Kibenge, FSB; Lopez, A
      Selection of an infectious bursal disease virus mutant with increased immunogenicity following passage under humoral immune pressure

      CANADIAN JOURNAL OF VETERINARY RESEARCH-REVUE CANADIENNE DE RECHERCHE VETERINAIRE
    98. Osei-Hyiaman, D; Hou, LF; Fan, MB; Ren, ZY; Zhang, ZM; Kano, K
      Coronary artery disease risk in Chinese type 2 diabetics: is there a role for paraxonase 1 gene (Q192R) polymorphism?

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    99. Messina, MF; De Luca, F; Wasniewska, M; Valenzise, M; Lombardo, F; Ghizzoni, L
      Final height in isolated GH deficiency type 1A: effects of 5-year treatment with IGF-I

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    100. Savage, PB
      Multidrug-resistant bacteria: overcoming antibiotic permeability barriers of Gram-negative bacteria

      ANNALS OF MEDICINE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 06/06/20 alle ore 23:58:33