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    1. Cao, A; Okamura, T; Ishiguro, C; Nakayama, K; Inoue, Y; Masuda, T
      Studies on syntheses and physical characterization of biodegradable aliphatic poly(butylene succinate-co-epsilon-caprolactone)s

      POLYMER
    2. Geromel, V; Cao, A; Briane, D; Vassy, J; Rotig, A; Rustin, P; Coudert, R; Rigaut, JP; Munnich, A; Taillandier, E
      Mitochondria transfection by oligonucleotides containing a signal peptide and vectorized by cationic liposomes

      ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT
    3. Crisponi, L; Deiana, M; Loi, A; Chiappe, F; Uda, M; Amati, P; Bisceglia, L; Zelante, L; Nagaraja, R; Porcu, S; Ristaldi, MS; Marzella, R; Rocchi, M; Nicolino, M; Lienhardt-Roussie, A; Nivelon, A; Verloes, A; Schlessinger, D; Gasparini, P; Bonneau, D; Cao, A; Pilia, G
      The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

      NATURE GENETICS
    4. Cao, A; Zhang, XF; Xu, CL; Liang, J; Wu, DH; Wei, BQ
      Aligned carbon nanotube growth under oxidative ambient

      JOURNAL OF MATERIALS RESEARCH
    5. Ristaldi, MS; Casula, S; Porcu, S; Cao, A
      Normal delta globin gene sequence in carrier of the silent-101 (C-T) beta-thalassemia mutation with normal HbA2 level

      AMERICAN JOURNAL OF HEMATOLOGY
    6. Ristaldi, MS; Drabek, D; Gribnau, J; Poddie, D; Yannoutsous, N; Cao, A; Grosveld, F; Imam, AMA
      The role of the-50 region of the human gamma-globin gene in switching

      EMBO JOURNAL
    7. He, Y; Shuai, XT; Cao, A; Kasuya, K; Doi, Y; Inoue, Y
      Enzymatic biodegradation of synthetic atactic poly(R,S-3-hydroxybutyrate) enhanced by an amorphous nonbiodegradable polymer

      POLYMER DEGRADATION AND STABILITY
    8. Cao, A; Welker, E; Scheraga, HA
      Effect of mutation of proline 93 on redox unfolding/folding of bovine pancreatic ribonuclease A

      BIOCHEMISTRY
    9. Gu, H; Cao, A; Walter, GH
      Host selection and utilisation of Sonchus oleraceus (Asteraceae) by Helicoverpa armigera (Lepidoptera : Noctuidae): A genetic analysis

      ANNALS OF APPLIED BIOLOGY
    10. Cao, A; Moi, P
      Genetic modifying factors in beta-thalassemia

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    11. Loudianos, G; Lovicu, M; Solinas, P; Kanavakis, E; Tzetis, M; Manolaki, N; Panagiotakaki, E; Karpathios, T; Cao, A
      Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations

      GENETIC TESTING
    12. Cao, A; Briane, D; Coudert, R; Vassy, J; Lievre, N; Olsman, E; Tamboise, E; Salzmann, JL; Rigaut, JP; Taillandier, E
      Delivery and pathway in MCF7 cells of DNA vectorized by cationic liposomesderived from cholesterol

      ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT
    13. Taillon-Miller, P; Bauer-Sardina, I; Saccone, NL; Putzel, J; Laitinen, T; Cao, A; Kere, J; Pilia, G; Rice, JP; Kwok, PY
      Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

      NATURE GENETICS
    14. Saxena, R; Moi, L; Demurtas, M; Rosatelli, MC; Cao, A; Verma, IC
      A beta-thalassaemia allele with 3 base substitution in codons 4/5 & 6 (ACTCCT GAG ACA TCT TAG) detected by denaturing gradient gel electrophoresis & sequencing

      INDIAN JOURNAL OF MEDICAL RESEARCH
    15. Cao, A
      Preventive genetics in 2000

      FETUS AS A PATIENT
    16. Barcia, R; Cao, A; Arbeteta, J; Ramos-Martinez, JI
      The IL-2 receptor in hemocytes of the sea mussel Mytilus galloprovincialisLmk

      IUBMB LIFE
    17. Ristaldi, MS; Casula, S; Porcu, S; Marongiu, MF; Pirastu, M; Cao, A
      Activation of the delta-globin gene by the beta-globin gene CACCC motif

      BLOOD CELLS MOLECULES AND DISEASES
    18. Pilia, G; Uda, M; Macis, D; Frau, F; Crisponi, L; Balli, F; Barbera, C; Colombo, C; Frediani, T; Gatti, R; Iorio, R; Marazzi, MG; Marcellini, M; Musumeci, S; Nebbia, G; Vajro, P; Ruffa, G; Zancan, L; Cao, A; DeVirgilis, S
      Jagged-1 mutation analysis in Italian Alagille syndrome patients

      HUMAN MUTATION
    19. Wang, Y; Ichikawa, M; Cao, A; Yoshie, N; Inoue, Y
      Comonomer composition distribution of P(3HB-co-3HP)s produced by Alcaligenes latus at several pH conditions

      MACROMOLECULAR CHEMISTRY AND PHYSICS
    20. Arai, Y; Cao, A; Yoshie, N; Inoue, Y
      Studies on comonomer compositional distribution and its effect on some physical properties of bacterial poly(3-hydroxybutyric acid-co-3-hydroxypropionic acid)

      POLYMER INTERNATIONAL
    21. Loudianos, G; Dessi, V; Lovicu, M; Angius, A; Pirastu, M; Cao, A
      Haplotype and mutation analysis in Mediterranean patients with Wilson disease

      JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    22. Galanello, R; Cipollina, MD; Dessi, C; Giagu, N; Lai, E; Cao, A
      Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia

      HAEMATOLOGICA
    23. Marwan, MM; Scerri, CA; Zarroag, SO; Cao, A; Kyrri, A; Kalogirou, E; Kleanthous, M; Ioannou, P; Angastiniotis, M; Felice, AE
      Comparative in vivo expression of beta(+)-thalassemia alleles

      HEMOGLOBIN
    24. Galanello, R; Cipollina, MD; Carboni, G; Perseu, L; Barella, S; Corrias, A; Cao, A
      Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome

      EUROPEAN JOURNAL OF PEDIATRICS
    25. Monni, G; Ibba, RM; Zoppi, MA; Putzolu, M; Floris, M; Cao, A
      Fetal nuchal translucency and prenatal diagnosis of beta-thalassaemia

      PRENATAL DIAGNOSIS
    26. He, Y; Masuda, T; Cao, A; Yoshie, N; Doi, Y; Inoue, Y
      Thermal, crystallization, and biodegradation behavior of poly(3-hydroxybutyrate) blends with poly (butylene succinate-co-butylene adipate) and poly(butylene succinate-co-epsilon-caprolactone)

      POLYMER JOURNAL
    27. Cao, A; Arai, Y; Yoshie, N; Kasuya, KI; Doi, Y; Inoue, Y
      Solid structure and biodegradation of the compositionally fractionated poly(3-hydroxybutyric acid-co-3-hydroxypropionic acid)s

      POLYMER
    28. Cao, A; Asakawa, N; Yoshie, N; Inoue, Y
      High-resolution solid-state C-13 n.m.r. study on phase structure of the compositionally fractionated bacterial copolyester poly(3-hydroxybutyric acid-co-3-hydroxypropionic acid)s

      POLYMER
    29. Loudianos, G; Dessi, V; Lovicu, M; Angius, A; Altuntas, B; Giacchino, R; Marazzi, M; Marcellini, M; Sartorelli, MR; Sturniolo, GC; Kocak, N; Yuce, A; Akar, N; Pirastu, M; Cao, A
      Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations

      JOURNAL OF MEDICAL GENETICS
    30. Paleari, R; Paglietti, E; Mosca, A; Mortarino, M; Maccioni, L; Satta, S; Cao, A; Galanello, R
      Posttranslational deamidation of proteins: The case of hemoglobin J Sardegna [alpha 50(CD8)His -> Asn -> Asp]

      CLINICAL CHEMISTRY
    31. Cazzola, M; Beguin, Y; Bergamaschi, G; Guarnone, R; Cerani, P; Barella, S; Cao, A; Galanello, R
      Soluble transferrin receptor as a potential determinant of iron loading incongenital anaemias due to ineffective erythropoiesis

      BRITISH JOURNAL OF HAEMATOLOGY
    32. Angius, A; Pisano, M; Manca, A; Casu, G; Persico, I; Pitzalis, S; De Gioia, E; Grignolo, FM; Loi, A; Sole, G; Cao, A; Spinelli, P; Ghillotti, G; Bonomi, L; Fossarello, M; Serra, A; Gandolfi, S; Alberti, G; Maraini, G; Serru, A; Orzalesi, N; Pirastu, M
      Molecular basis of open-angle glaucoma in Italy

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    33. LOUDIANOS G; DESSI V; LOVICU M; ANGIUS A; NURCHI A; STURNIOLO GC; MARCELLINI M; ZANCAN L; BRAGETTI P; AKAR N; YAGCI R; VEGNENTE A; CAO A; PIRASTU M
      FURTHER DELINEATION OF THE MOLECULAR PATHOLOGY OF WILSON-DISEASE IN THE MEDITERRANEAN POPULATION

      Human mutation
    34. LEONI GB; PITZALIS S; TONELLI R; CAO A
      IDENTIFICATION OF A NOVEL MUTATION (S13F) IN THE CFTR GENE IN A CF PATIENT OF SARDINIAN ORIGIN

      Human mutation
    35. MELIS MA; MUNTONI F; CAU M; LOI D; PUDDU A; BOCCONE L; MATEDDU A; CIANCHETTI C; CAO A
      NOVEL NONSENSE MUTATION (C-]A NT-10512) IN EXON-72 OF DYSTROPHIN GENELEADING TO EXON SKIPPING IN A PATIENT WITH A MILD DYSTROPHINOPATHY

      Human mutation
    36. Pellegrini, M; Pilia, G; Pantano, S; Lucchini, F; Uda, M; Fumi, M; Cao, A; Schlessinger, D; Forabosco, A
      Gpc3 expression correlates with the phenotype of the Simpson-Golabi-Behmelsyndrome

      DEVELOPMENTAL DYNAMICS
    37. LOUDIANOS G; DESSI V; LOVICU M; ANGIUS A; KANAVAKIS E; TZETIS M; KATTAMIS C; MANOLAKI N; VASSILIKI G; KARPATHIOS T; CAO A; PIRASTU M
      HAPLOTYPE AND MUTATION ANALYSIS IN GREEK PATIENTS WITH WILSON-DISEASE

      European journal of human genetics
    38. ANTONARAKIS SE; NAGAMINE K; PETERSON P; ROSATELLI MC; LALIOTI MD; MULLIS PE; BETTERLE C; COHEN A; SERI M; LERONE M; ROMEO G; CAO A; KUDOH J; KROHN KJE; SHIMIZU N; SCOTT HS
      IDENTIFICATION OF A POTENTIAL TRANSCRIPTION REGULATOR MUTATED IN AUTOIMMUNE POLYGLANDULAR DISEASE-1

      European journal of human genetics
    39. LIBERT F; COCHAUX P; BECKMAN G; SAMSON M; AKSENOVA M; CAO A; CZEIZEL A; CLAUSTRES M; DELARUA C; FERRARI M; FERREC C; GLOVER G; GRINDE B; GURAN S; KUCINSKAS V; LAVINHA J; MERCIER B; OGUR G; PELTONEN L; ROSATELLI C; SCHWARTZ M; SPITSYN V; TIMAR L; BECKMAN L; PARMENTIER M; VASSART G
      THE DELTA-CCR5 MUTATION CONFERRING PROTECTION AGAINST HIV-1 IN CAUCASIAN POPULATIONS HAS A SINGLE AND RECENT ORIGIN IN NORTHEASTERN EUROPE

      Human molecular genetics
    40. Cao, A; Galanello, R; Rosatelli, MC
      Prenatal diagnosis and screening of the haemoglobinopathies

      BAILLIERES CLINICAL HAEMATOLOGY
    41. PAGLIETTI E; BARELLA S; SATTA S; PERRA C; CAO A; GALANELLO R
      HB-SASSARI[ALPHA-126(H9)ASP-]HIS] RESULTS FROM A (G)UNDER-BAR-AC-](C)UNDER-BAR-AC MUTATION IN THE ALPHA-1-GLOBIN GENE

      Hemoglobin
    42. GALANELLO R; SOLLAINO C; PAGLIETTI E; BARELLA S; PERRA C; DONEDDU I; PIRRONI MG; MACCIONI L; CAO A
      ALPHA-THALASSEMIA CARRIER IDENTIFICATION BY DNA ANALYSIS IN THE SCREENING FOR THALASSEMIA

      American journal of hematology
    43. GASPERINI D; PERSEU L; MELIS MA; MACCIONI L; SOLLAINO MC; PAGLIETTI E; CAO A; GALANELLO R
      HETEROZYGOUS BETA-THALASSEMIA WITH THALASSEMIA-INTERMEDIA PHENOTYPE

      American journal of hematology
    44. Rosatelli, MC; Meloni, A; Meloni, A; Devoto, M; Cao, A; Scott, HS; Peterson, P; Heino, M; Krohn, KJE; Nagamine, K; Kudoh, J; Shimizu, N; Antonarakis, SE
      A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients

      HUMAN GENETICS
    45. ANGIUS A; DESSI V; LOVICU M; DEVIRGILIIS S; PIRASTU M; CAO A
      EARLY AND SEVERE NEUROLOGICAL FEATURES IN A WILSON-DISEASE PATIENT COMPOUND HETEROZYGOUS FOR 2 FRAMESHIFT MUTATIONS

      European journal of pediatrics
    46. CAO A; ASAKAWA N; YOSHIE N; INOUE Y
      PHASE-STRUCTURE AND BIODEGRADATION OF THE BACTERIAL POLY(3-HYDROXYBUTYRIC ACID) CHEMOSYNTHETIC POLY(3-HYDROXYPROPIONIC ACID) BLEND/

      Polymer Journal
    47. CAO A; KASUYA K; ABE H; DOI Y; INOUE Y
      STUDIES ON COMONOMER COMPOSITIONAL DISTRIBUTION OF THE BACTERIAL POLY(3-HYDROXYBUTYRIC ACID-CO-3-HYDROXYPROPIONIC ACID)S AND CRYSTAL AND THERMAL-CHARACTERISTICS OF THEIR FRACTIONATED COMPONENT COPOLYESTERS

      Polymer
    48. CUCCA F; ZHU ZB; KHANNA A; COSSU F; CONGIA M; BADIALI M; LAMPIS R; FRAU F; DEVIRGILIIS S; CAO A; ARNONE M; PIRAS P; CAMPBELL RD; COOPER MD; VOLANAKIS JE; POWIS SH
      EVALUATION OF IGA DEFICIENCY IN SARDINIANS INDICATES A SUSCEPTIBILITYGENE IS ENCODED WITHIN THE HLA CLASS-III REGION

      Clinical and experimental immunology
    49. ANGIUS A; DEGIOIA E; LOI A; FOSSARELLO M; SOLE G; ORZALESI N; GRIGNOLO F; CAO A; PIRASTU M
      A NOVEL MUTATION IN THE GLC1A GENE CAUSES JUVENILE OPEN-ANGLE GLAUCOMA IN 4 FAMILIES FROM THE ITALIAN REGION OF PUGLIA

      Archives of ophthalmology
    50. LOUDIANOS G; DESSI V; LOVICU M; ANGIUS A; CAO A; PIRASTU M
      THE -75A-]C SUBSTITUTION IN THE 5'-UTR OF THE WILSON DISEASE GENE IS A SEQUENCE POLYMORPHISM IN THE MEDITERRANEAN POPULATION

      American journal of human genetics
    51. CAO A; ICHIKAWA M; IKEJIMA T; YOSHIE N; INOUE Y
      THERMAL AND MORPHOLOGICAL-STUDY OF FRACTIONATED POLY(3-HYDROXYBUTYRICACID-CO-3-HYDROXYPROPIONIC ACID)

      Macromolecular chemistry and physics
    52. PIEMONTESE MR; MEMEO E; CARELLA M; AMATI P; CHOMEL JC; BONNEAU D; PILIA G; CAO A; DRABKIN H; GEMMILL R; ROMMENS J; ZELANTE L; GASPARINI P; BISCEGLIA L
      A YAC CONTIG SPANNING THE BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUSSYNDROME AND PROPIONIC ACIDEMIA LOCI

      European journal of human genetics
    53. HUBER R; CRISPONI L; MAZZARELLA R; CHEN CN; SU Y; SHIZUYA H; CHEN EY; CAO A; PILIA G
      ANALYSIS OF EXON INTRON STRUCTURE AND 400 KB OF GENOMIC SEQUENCE SURROUNDING THE 5'-PROMOTER AND 3'-TERMINAL ENDS OF THE HUMAN GLYPICAN 3 (GPC3) GENE/

      Genomics
    54. PUTZOLU M; MELONI A; LOCHE S; PISCHEDDA C; CAO A; MOI P
      A HOMOZYGOUS NONSENSE MUTATION OF THE HUMAN GROWTH-HORMONE RECEPTOR GENE IN A SARDINIAN BOY WITH LARON-TYPE DWARFISM

      Journal of endocrinological investigation
    55. ZHANG X; ZHENG Y; CHEN H; WANG S; CAO A; PENG B; NAN R
      THE MIYUN 232 MHZ SURVEY .2. THE MAIN LIST

      Astronomy & Astrophysics. Supplement series
    56. GALANELLO R; PALEARI R; PERSEU L; BARELLA S; MACCIONI L; CAO A; MULAS G; COCCO E; MOSCA A
      HB PUTTELANGE [BETA-140(H19)ALA-]VAL] IN AN ITALIAN MAN WITH POLYCYTHEMIA

      Hemoglobin
    57. MURRU S; PANI L; PODDIE D; GESSA G; CAO A; PIRASTU M
      RAT TYROSINE-HYDROXYLASE GENE POLYMORPHISMS

      Molecular brain research
    58. FOSSARELLO M; ZUCCA I; GALANTUOMO S; SERRA A; PIRASTU M; LOI A; SOLE G; CAO A
      GENETIC-MAPPING OF AUTOSOMAL-DOMINANT PRIMARY OPEN-ANGLE GLAUCOMA (POAG) IN SARDINIA

      International ophtalmology
    59. CAO A; SABA L; GALANELLO R; ROSATELLI C
      MOLECULAR DIAGNOSIS AND CARRIER SCREENING FOR BETA-THALASSEMIA

      JAMA, the journal of the American Medical Association
    60. MATHEU V; GRACIA MT; CABRERIZO S; SIERRA Z; CAO A; ZUBELDIA JM; BAEZA ML
      FISH AVOIDANCE IN ANISAKIS SENSITIZED PATIENTS

      Journal of allergy and clinical immunology
    61. ROSATELLI MC; MELONI A; FAA V; SABA L; CRISPONI G; CLEMENTE MG; MELONI G; PIGA MT; CAO A
      MOLECULAR ANALYSIS OF PATIENTS OF SARDINIAN DESCENT WITH CRIGLER-NAJJAR SYNDROME TYPE-I

      Journal of Medical Genetics
    62. MARINI MG; CHAN K; CASULA L; KAN YW; CAO A; MOI P
      HMAF, A SMALL HUMAN TRANSCRIPTION FACTOR THAT HETERODIMERIZES SPECIFICALLY WITH NRF1 AND NRF2

      The Journal of biological chemistry
    63. GALANELLO R; PERSEU L; MELIS MA; CIPOLLINA L; BARELLA S; GIAGU N; TURCO MP; MACCIONI O; CAO A
      HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA IS RELATED TO CO-INHERITED GILBERTS-SYNDROME

      British Journal of Haematology
    64. MOI P; ASUNIS I; CASULA S; CAO A
      AN ERYTHROID KRUPPEL-LIKE FACTOR ENGINEERED TO PREFERENTIALLY BIND THE GAMMA-GLOBIN GENE PROMOTER

      Blood
    65. GALANELLO R; CIPOLLINA L; BARELLA LS; GIAGU L; LAI E; CAO A
      HYPERBILIRUBINEMIA AND GILBERTS-SYNDROME IN THALASSEMIA MAJOR AND INTERMEDIA

      Blood
    66. RENDINE S; CALAFELL F; CAPPELLO N; GAGLIARDINI R; CARAMIA G; RIGILLO N; SILVETTI M; ZANDA M; MIANO A; BATTISTINI F; MARIANELLI L; TACCETTI G; DIANA MC; ROMANO L; ROMANO C; GIUNTA A; PADOAN R; PIANAROLI A; RAIA V; DERITIS G; BATTISTINI A; GRZINCICH G; JAPICHINO L; PARDO F; ANTONELLI M; QUATTRUCCI S; LUCIDI V; CASTRO M; SANTINI B; CASTELLO M; GUANTI G; LEONI GB; CAO A; TOFFOLI C; LUCCI E; VULLO C; TORRICELLI F; SBERNINI F; ROMEO G; RONCHETTO P; SEIA M; ROSSI A; FERRARI M; CREMONESI L; SALVATORE F; CASTALDO G; DALCAMO E; MAGGIO A; SANGIUOLO F; DALLAPICCOLA B; MACERATESI P; BISCEGLIA L; GASPARINI P; CARBONARA A; BONIZZATO A; CABRINI G; BOMBIERI C; PIGNATTI PF; BORGO G; CASTELLANI C; VILLANI A; ARDUINO C; SALVATORE D; MASTELLA G; PIAZZA A
      GENETIC HISTORY OF CYSTIC-FIBROSIS MUTATIONS IN ITALY - I - REGIONAL DISTRIBUTION

      Annals of Human Genetics
    67. PORRU D; PAU AC; SCARPA RM; ZANOLLA L; CAO A; USAI E
      BEHCETS-DISEASE AND THE NEUROPATHIC BLADDER - URODYNAMIC FEATURES - CASE-REPORT AND A LITERATURE-REVIEW

      Spinal cord
    68. PILIA G; HUGHESBENZIE RM; MACKENZIE A; BAYBAYAN P; CHEN EY; HUBER R; NERI G; CAO A; FORABOSCO A; SCHLESSINGER D
      MUTATIONS IN GPC3, A GLYPICAN GENE, CAUSE THE SIMPSON-GOLABI-BEHMEL OVERGROWTH SYNDROME

      Nature genetics
    69. MELONI A; MELONI A; CAO A; ROSATELLI MC
      NEW FRAMESHIFT MUTATION IN THE DAX-1 GENE IN A PATIENT WITH X-LINKED ADRENAL HYPOPLASIA AND HYPOGONADOTROPIC HYPOGONADISM

      Human mutation
    70. COCCO S; MELONI A; MARINI MG; CAO A; MOI P
      A MISSENSE (T577I) MUTATION IN THE LUTEINIZING-HORMONE RECEPTOR GENE ASSOCIATED WITH FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY

      Human mutation
    71. CASULA L; ARCHIDIACONO N; PAU MG; ADDIS M; MURA R; GALANELLO R; BIDDAU P; CAO A; NUCARO A
      CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF A VARIANT TRANSLOCATIONASSOCIATED WITH ACUTE PROMYELOCYTIC LEUKEMIA AND INVOLVING CHROMOSOME-11, CHROMOSOME-15 AND CHROMOSOME-17

      Leukemia
    72. HEALY MJ; DUMANCIC MM; CAO A; OAKESHOTT JG
      LOCALIZATION OF SEQUENCES REGULATING ANCESTRAL AND ACQUIRED SITES OF ESTERASE6 ACTIVITY IN DROSOPHILA-MELANOGASTER

      Molecular biology and evolution
    73. FRISCHKNECHT H; VENTRUTO M; HESS D; HUNZIKER P; ROSATELLI MC; CAO A; BREITENSTEIN U; FEHR J; TUCHSCHMID P
      HB HINWIL OR BETA-38(C4)THR-]ASN - A NEW BETA-CHAIN VARIANT DETECTED IN A SWISS FAMILY

      Hemoglobin
    74. LOUDIANOS G; DESSI V; ANGIUS A; LOVICU M; LOI A; DEIANA M; AKAR N; VAJRO P; FIGUS A; CAO A; PIRASTU M
      WILSON DISEASE MUTATIONS ASSOCIATED WITH UNCOMMON HAPLOTYPES IN MEDITERRANEAN PATIENTS

      Human genetics
    75. CONGIA M; CLEMENTE MG; DESSI C; CUCCA F; MAZZOLENI AP; FRAU F; LAMPIS R; CAO A; LAI ME; DEVIRGILIIS S
      HLA CLASS-II GENES IN CHRONIC HEPATITIS-C VIRUS-INFECTION AND ASSOCIATED IMMUNOLOGICAL DISORDERS

      Hepatology
    76. CAO A; GALANELLO R; ROSATELLI MC; ARGIOLU F; DEVIRGILIIS S
      CLINICAL-EXPERIENCE OF MANAGEMENT OF THALASSEMIA - THE SARDINIAN EXPERIENCE

      Seminars in hematology
    77. CAO A; ICHIKAWA M; KASUYA KI; YOSHIE N; ASAKAWA N; INOUE Y; DOI Y; ABE H
      COMPOSITION FRACTIONATION AND THERMAL CHARACTERIZATION OF POLY(3-HYDROXYBUTYRATE-CO-3-HYDROXYPROPIONATE)

      Polymer Journal
    78. GALANELLO R; PERSEU L; MELIS MA; BARELLA S; GIAGU N; TURCO MP; MACCIONI O; CAO A
      GENETIC-BASIS OF HYPERBILIRUBINEMIA IN HETEROZYGOUS BETA-THALASSEMIA

      Blood
    79. MOI P; SENES G; AZUNIS I; CASULA S; SABA L; ROSATELLI C; CAO A
      HUMAN EKLF BINDING AND TRANSACTIVATION FROM WILD-TYPE AND MUTANT CACCC BOXES

      Blood
    80. FOSSARELLO M; BERTINI C; GALANTUOMO MS; CAO A; SERRA A; PIRASTU M
      DELETION IN THE PERIPHERIN RDS GENE IN 2 UNRELATED SARDINIAN FAMILIESWITH AUTOSOMAL-DOMINANT BUTTERFLY-SHAPED MACULAR DYSTROPHY

      Archives of ophthalmology
    81. PANI A; ALTIERI P; DEVIRGILIIS S; CAO A; LAMPIS R; FRAU F; MELIS P; ARNONE M; PIRAS P; FRESU A; CUCCA F; CONGIA M
      STRONG ASSOCIATION OF HLA-DQB2 IN SARDINIAN PATIENTS WITH IDIOPATHIC MEMBRANOUS NEPHROPATHY

      Journal of the American Society of Nephrology
    82. DESSI C; CLEMENTE MG; DIANA G; CONGIA M; FRAU F; LAI ME; MAZZOLENI AP; BALESTRIERI A; CENGIAROTTI L; PIANO P; DELGIACCO S; LILLIU F; CORNACCHIA G; MURONI PP; CAO A; DEVIRGILIIS S
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 03:17:18