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    1. Radu, P; Atsmon, J
      Gilbert's syndrome - Clinical and pharmacological implications

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    2. Weatherall, DJ
      Phenotype-genotype relationships in monogenic disease: Lessons from the thalassaemias

      NATURE REVIEWS GENETICS
    3. Oleksiak, MF; Kolell, KJ; Crawford, DL
      Utility of natural populations for microarray analyses: Isolation of genesnecessary for functional genomic studies

      MARINE BIOTECHNOLOGY
    4. Vrieling, H
      Mitotic maneuvers in the light

      NATURE GENETICS
    5. Shao, CS; Stambrook, PJ; Tischfield, JA
      Mitotic recombination is suppressed by chromosomal divergence in hybrids of distantly related mouse strains

      NATURE GENETICS
    6. Huang, CS; Luo, GA; Huang, MJ; Chen, ES; Young, TH; Chao, YC
      A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes Crigler-Najjar syndrome type II

      PHARMACOGENETICS
    7. Qureshi, AA; Sami, SA; Salser, WA; Khan, FA
      Synergistic effect of tocotrienol-rich fraction (TRF25) of rice bran and lovastatin on lipid parameters in hypercholesterolemic humans

      JOURNAL OF NUTRITIONAL BIOCHEMISTRY
    8. Caprari, P; Caforio, MP; Cianciulli, P; Maffi, D; Pasquino, MT; Tarzia, A; Amadori, S; Salvati, AM
      6-phosphogluconate dehydrogenase deficiency in an Italian family

      ANNALS OF HEMATOLOGY
    9. Auchus, RJ
      The genetics, pathophysiology, and management of human deficiencies of P450c17

      ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA
    10. Subar, M
      Clinical evaluation of hypercoagulable states

      CLINICS IN GERIATRIC MEDICINE
    11. Traeger-Synodinos, J; Papassotiriou, I; Vrettou, C; Skarmoutsou, C; Stamoulakatou, A; Kanavakis, E
      Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional alpha-globin and beta-globin gene

      HAEMATOLOGICA
    12. Tsuda, M; Sanada, M; Nakagawa, H; Kodama, I; Sakashita, T; Ohama, K
      Phenotype of apolipoprotein E influences the lipid metabolic response of postmenopausal women to hormone replacement therapy

      MATURITAS
    13. Wu, JS; Gu, JM; Xu, J; Wang, J; Sun, ZM; Smirnov, MD; Morrissey, JH; Esmon, N
      Factor V Leiden mutation in one family of Chinese origin

      CHINESE MEDICAL JOURNAL
    14. Perry, MG; Molero, MM; Giulumian, AD; Katakam, PVG; Pollock, JS; Pollock, DM; Fuchs, LC
      ETB receptor-deficient rats exhibit reduced contraction to ET-1 despite anincrease in ETA receptors

      AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
    15. Ishihara, H; Kanda, F; Nishio, H; Sumino, K; Chihara, K
      Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy

      JOURNAL OF NEUROLOGY
    16. Van Oeckel, MJ; Warnants, N; Boucque, CV; Delputte, P; Depuydt, J
      The preference of the consumer for pork from homozygous or heterozygous halothane negative animals

      MEAT SCIENCE
    17. Real, JT; Chaves, FJ; Martinez-Uso, I; Garcia-Garcia, AB; Ascaso, JF; Carmena, R
      Importance of HDL cholesterol levels and the total/HDL cholesterol ratio as a risk factor for coronary heart disease in molecularly defined heterozygous familial hypercholesterolaemia

      EUROPEAN HEART JOURNAL
    18. Ogura, H; Matsumoto, M; Mikoshiba, K
      Motor discoordination in mutant mice heterozygous for the type 1 inositol 1,4,5-trisphosphate receptor

      BEHAVIOURAL BRAIN RESEARCH
    19. Rivero, MB; Olicio, R; Lima, CR; Bonvicino, CR; Moreira, MAM; Llerena, JC; Seuanez, HN
      Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrierof an HPRT1 mutation responsible for Lesch-Nyhan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    20. Sasaki, R; Ito, N; Shimamura, M; Murakami, T; Kuzuhara, S; Uchino, M; Uyama, E
      A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotoniacongenita

      MUSCLE & NERVE
    21. Kobayashi, T; Homma, Y
      Effects of low-dose pravastatin on plasma levels of lipids and apolipoproteins in Japanese type II hyperlipoproteinemic subjects with apolipoprotein E phenotype E3/2, E3/3, and E4/3

      JOURNAL OF CLINICAL PHARMACOLOGY
    22. Beutler, E; Felitti, V; Gelbart, T; Ho, N
      Genetics of iron storage and hemochromatosis

      DRUG METABOLISM AND DISPOSITION
    23. Illingworth, DR; Tobert, JA
      HMG-CoA reductase inhibitors

      ADVANCES IN PROTEIN CHEMISTRY, VOL 56
    24. Gidding, SS
      Cholesterol guidelines debate

      PEDIATRICS
    25. Real, JT; Chaves, FJ; Civera, M; Garcia-Garcia, AB; Ascaso, JF; Armengod, ME; Carmena, R
      Influence of FH Valencia 1 and 2 mutations of the LDL receptor gene on theresponse to simvastatin in subjects with molecularly defined heterozygous familial hypercholesterolemia in Spain

      MEDICINA CLINICA
    26. Li, SR; Koller, E; Valent, P; Gludovacz, D; Yang, Q; Patri, P; Angelberger, P; Dudczak, R; Virgolini, I
      Effects of vasoactive intestinal peptide (VIP) and somatostatin (SST) on lipoprotein receptor expression by A431 tumor cells

      LIFE SCIENCES
    27. Boehmer, ALM; Nijman, RJM; Lammers, BAS; De Coninck, SJF; Van Hemel, JO; Themmen, APN; Mureau, MAM; De Jong, FH; Brinkmann, AO; Niermeijer, MF; Drop, SLS
      Etiological studies of severe or familial hypospadias

      JOURNAL OF UROLOGY
    28. Tarugi, P; Lonardo, A; Gabelli, C; Sala, F; Ballarini, G; Cortella, I; Previato, L; Bertolini, S; Cordera, R; Calandra, S
      Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene

      JOURNAL OF LIPID RESEARCH
    29. Solis, C; Aizencang, GI; Astrin, KH; Bishop, DF; Desnick, R
      Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria

      JOURNAL OF CLINICAL INVESTIGATION
    30. Pedro-Botet, J; Schaefer, EJ; Bakker-Arkema, RG; Black, DM; Stein, EM; Corella, D; Ordovas, JM
      Apolipoprotein E genotype affects plasma lipid response to atorvastatin ina gender specific manner

      ATHEROSCLEROSIS
    31. Gardner, M; Fowler, K; Partridge, L; Barton, N
      Genetic variation for preadult viability in Drosophila melanogaster

      EVOLUTION
    32. Brorholt-Petersen, JU; Jensen, HK; Raungaard, B; Gregersen, N; Faergeman, O
      LDL-receptor gene mutations and the hypocholesterolemic response to statintherapy

      CLINICAL GENETICS
    33. Tekin, M; Arnos, KS; Xia, XJ; Oelrich, MK; Liu, XZ; Nance, WE; Pandya, A
      W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness

      CLINICAL GENETICS
    34. Wilmink, HW; Twickler, MB; Banga, JD; Dallinga-Thie, GM; Eeltink, H; Erkelens, DW; Rabelink, TJ; Stroes, ES
      Effect of statin versus fibrate on postprandial endothelial dysfunction: role of remnant-like particles

      CARDIOVASCULAR RESEARCH
    35. Favier, R; Aoki, N; de Moerloose, P
      Congenital alpha(2)-plasmin inhibitor deficiencies: a review

      BRITISH JOURNAL OF HAEMATOLOGY
    36. Wada, Y; Abe, T; Sato, H; Tamai, M
      A novel Gly35Ser mutation in the RDH5 gene in a Japanese family with fundus albipunctatus associated with cone dystrophy

      ARCHIVES OF OPHTHALMOLOGY
    37. Primhak, RA; Tanner, MS
      Alpha-1 antitrypsin deficiency

      ARCHIVES OF DISEASE IN CHILDHOOD
    38. Ginsberg, HN
      Hypertriglyceridemia: New insights and new approaches to pharmacologic therapy

      AMERICAN JOURNAL OF CARDIOLOGY
    39. Koks, S; Volke, V; Veraksits, A; Runkorg, K; Sillat, T; Abramov, U; Bourin, M; Huotari, M; Mannisto, PT; Matsui, T; Vasar, E
      Cholecystokinin(2) receptor-deficient mice display altered function of brain dopaminergic system

      PSYCHOPHARMACOLOGY
    40. Miyazaki, K; Maeda, H; Sunagawa, M; Tamai, Y; Shiraishi, S
      Screening of heterozygous DNA markers in shiitake (Lentinula edodes) usingde-dikaryotization via preparation of protoplasts and isolation of four meiotic monokaryons from one basidium

      JOURNAL OF WOOD SCIENCE
    41. Siest, G; Bertrand, P; Herbeth, B; Vincent-Viry, M; Schiele, F; Sass, C; Visvikis, S
      Apolipoprotein E polymorphisms and concentration in chronic diseases and drug responses

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    42. Ekstrom, U; Abrahamson, M; Sveger, T; Sun, XM; Soutar, AK; Nilsson-Ehle, P
      Expression of an LDL receptor allele with two different mutations (E256K and I402T)

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    43. Mauvais-Jarvis, F; Kahn, CR
      Understanding the pathogenesis and treatment of insulin resistance and type 2 diabetes mellitus: What can we learn from transgenic and knockout mice?

      DIABETES & METABOLISM
    44. Mitsumori, K; Shimo, T; Onodera, H; Takagi, H; Yasuhara, K; Tamura, T; Aoki, Y; Nagata, O; Hirose, M
      Modifying effects of ethinylestradiol but not methoxychlor on N-ethyl-N-nitrosourea-induced uterine carcinogenesis in heterozygous p53-deficient CBA mice

      TOXICOLOGICAL SCIENCES
    45. Hagberg, JM; Wilund, KR; Ferrell, RE
      APO E gene and gene-environment effects on plasma lipoprotein-lipid levels

      PHYSIOLOGICAL GENOMICS
    46. Phelan, JK; Bok, D
      A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes

      MOLECULAR VISION
    47. Leviev, I; James, RW
      Promoter polymorphisms of human paraoxonase PON1 gene and serum paraoxonase activities and concentrations

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    48. Twickler, TB; Dallinga-Thie, GM; de Valk, HW; Schreuder, PCNJ; Jansen, H; Cabezas, MC; Erkelens, DW
      High dose of simvastatin normalizes postprandial remnant-like particle response in patients with heterozygous familial hypercholesterolemia

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    49. Levy, E; Bendayan, M
      Use of immunoelectron microscopy and intestinal models to explore the elaboration of apolipoproteins required for intraenterocyte lipid transport

      MICROSCOPY RESEARCH AND TECHNIQUE
    50. Wilke, K; Duman, B; Horst, J
      Diagnosis of haploidy and triploidy based on measurement of gene copy number by real-time PCR

      HUMAN MUTATION
    51. Saint-Jore, B; Varret, M; Dachet, C; Rabes, JP; Devillers, M; Erlich, D; Blanchard, P; Krempf, M; Mathe, D; Chanu, B; Jacotot, B; Farnier, M; Bonaiti-Pellie, C; Junien, C; Boileau, C
      Autosomal dominant type IIa hypercholesterolemia: evaluation of the respective contributions of LDLR and APOB gene defects as well as a third major group of defects

      EUROPEAN JOURNAL OF HUMAN GENETICS
    52. Pauletto, P; Puato, M; Faggin, E; Sartore, S
      Low-dose cerivastatin inhibits spontaneous atherogenesis in heterozygous Watanabe hyperlipidemic rabbits

      JOURNAL OF VASCULAR RESEARCH
    53. Mariotti, C; Castellotti, B; Pareyson, D; Testa, D; Eoli, M; Antozzi, C; Silani, V; Marconi, R; Tezzon, F; Siciliano, G; Marchini, C; Gellera, C; Di Donato, S
      Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families

      NEUROMUSCULAR DISORDERS
    54. Huang, CS; Luo, GA; Huang, MJ; Yu, SC; Yang, SS
      Variations of the bilirubin uridine-diphosyphoglucuronosyl transferase 1A1gene in healthy Taiwanese

      PHARMACOGENETICS
    55. Takagi, A; Ikeda, Y; Takeda, E; Yamamoto, A
      A newly identified lipoprotein lipase (LPL) gene mutation (F270L) in a Japanese patient with familial LPL deficiency

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    56. Yan, XH; Fujita, Y; Aruga, Y
      Induction and characterization of pigmentation mutants in Porphyra yezoensis (Bangiales, Rhodophyta)

      JOURNAL OF APPLIED PHYCOLOGY
    57. Salazar, LA; Hirata, MH; Quintao, ECR; Hirata, RDC
      Lipid-lowering response of the HMG-CoA reductase inhibitor fluvastatin is influenced by polymorphisms in the low-density lipoprotein receptor gene inBrazilian patients with primary hypercholesterolemia

      JOURNAL OF CLINICAL LABORATORY ANALYSIS
    58. Rawool, NM; Nazarian, LN
      Ultrasound of the ankle and foot

      SEMINARS IN ULTRASOUND CT AND MRI
    59. Ballantyne, CM; Herd, JA; Stein, EA; Ferlic, LL; Dunn, JK; Gotto, AM; Marian, AJ
      Apolipoprotein E genotypes and response of plasma lipids and progression-regression of coronary atherosclerosis to lipid-lowering drug therapy

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    60. Akosah, KO; Gower, E; Groon, L; Rooney, BL; Schaper, A
      Mild hypercholesterolemia and premature heart disease: Do the national criteria underestimate disease risk?

      JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
    61. Cerda-Flores, RM; Davila-Rodriguez, MI
      Natural fertility in northeastern Mexico: Genetic structure by year of birth and birthplace

      ARCHIVES OF MEDICAL RESEARCH
    62. Sauer, I; Klein, B; Leeners, B; Cotarelo, C; Heyl, W; Funk, A
      Lethal osteochondrodysplasias: Praenatal and postnatal differential diagnosis.

      ULTRASCHALL IN DER MEDIZIN
    63. Raijmakers, MTM; Jansen, PLM; Steegers, EAP; Peters, WHM
      Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene

      JOURNAL OF HEPATOLOGY
    64. Tarugi, P; Lonardo, A; Ballarini, G; Erspamer, L; Tondelli, E; Bertolini, S; Calandra, S
      A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5)

      JOURNAL OF HEPATOLOGY
    65. Cicero, AFG; Braiato, A; D'Addato, S; Sangiorgi, Z; Gaddi, A
      A suggestion for familial hypercholesterolemia (FH) heterozygosity clinical diagnosis based on epidemiological observations in a large Italian population

      INTERNATIONAL JOURNAL OF CARDIOLOGY
    66. Navarro, P; Christensen, RK; Weber, P; Rothschild, M; Ekhardt, G; Butler, JE
      Porcine IgA allotypes are not equally transcribed or expressed in heterozygous swine

      MOLECULAR IMMUNOLOGY
    67. Takano, A; Bonnemann, CG; Honda, H; Sakai, M; Feener, CA; Kunkel, LM; Sobue, G
      Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations

      MUSCLE & NERVE
    68. Ikeda, Y; Goji, K; Takagi, A
      A compound heterozygote for a novel missense mutation (G 105R) in exon 3 and a missense mutation (D204E) in exon 5 of the lipoprotein lipase gene in a Japanese infant with hyperchylomicronaemia

      CLINICAL SCIENCE
    69. Sinzinger, H; Chehne, F; Schmid, P; Kritz, H
      Plasma homocysteine is not altered during simvastatin-therapy

      WIENER KLINISCHE WOCHENSCHRIFT
    70. Dobs, AS; Schrott, H; Davidson, MH; Bays, H; Stein, EA; Kush, D; Wu, M; Mitchel, Y; Illingworth, RD
      Effects of high-dose simvastatin on adrenal and gonadal steroidogenesis inmen with hypercholesterolemia

      METABOLISM-CLINICAL AND EXPERIMENTAL
    71. Dobs, AS; Miller, S; Neri, G; Weiss, S; Tate, AC; Shapiro, DR; Musliner, TA
      Effects of simvastatin and pravastatin on gonadal function in male hypercholesterolemic patients

      METABOLISM-CLINICAL AND EXPERIMENTAL
    72. Illingworth, R
      Management of hypercholesterolemia

      MEDICAL CLINICS OF NORTH AMERICA
    73. Heath, KE; Whittall, RA; Miller, GJ; Humphries, SE
      I705 variant in the low density lipoprotein receptor gene has no effect onplasma cholesterol levels

      JOURNAL OF MEDICAL GENETICS
    74. Parhofer, KG; Barrett, PHR; Demant, T; Schwandt, P
      Acute effects of low density lipoprotein apheresis on metabolic parametersof apolipoprotein B

      JOURNAL OF LIPID RESEARCH
    75. Ingram, DA; Yang, FC; Travers, JB; Wenning, MJ; Hiatt, K; New, S; Hood, A; Shannon, K; Williams, DA; Clapp, DW
      Genetic and biochemical evidence that haploinsufficiency of the Nf1 tumor suppressor gene modulates melanocyte and mast cell fates in vivo

      JOURNAL OF EXPERIMENTAL MEDICINE
    76. Blason-Lauber, A; Kempken, B; Werder, E; Forest, MG; Einaudi, S; Ranke, MB; Matsuo, N; Brunelli, V; Schonle, EJ; Zachmann, M
      17 alpha-hydroxylase/17,20-lyase deficiency as a model to study enzymatic activity regulation: Role of phosphorylation

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    77. Chen, ZJ; Fitzgerald, RL; Averna, MR; Schonfeld, G
      A targeted apolipoprotein B-38.9-producing mutation causes fatty livers inmice due to the reduced ability of apolipoprotein B-38.9 to transport triglycerides

      JOURNAL OF BIOLOGICAL CHEMISTRY
    78. Muradov, KG; Artemyev, NO
      Loss of the effector function in a transducin-alpha mutant associated withNougaret night blindness

      JOURNAL OF BIOLOGICAL CHEMISTRY
    79. Frikke-Schmidt, R; Wittrup, HH; Tybjaerg-Hansen, A; Meinertz, H; Schnohr, P; Nordestgaard, BG
      Apolipoprotein E genotypes predict attendance rates at lipid clinic

      ATHEROSCLEROSIS
    80. Sniderman, AD; Zhang, XJ; Cianflone, K
      Governance of the concentration of plasma LDL: a reevaluation of the LDL receptor paradigm

      ATHEROSCLEROSIS
    81. Chan, L; Mak, Y; Tomlinson, B; Baum, L; Wu, X; Masarei, J; Pang, C
      Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a Chinese patient with hypertriglyceridemia

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    82. Singh, BN
      Drosophila ananassae: A species characterized by several unusual genetic features

      CURRENT SCIENCE
    83. Raungaard, B; Jensen, HK; Brorholt-Petersen, JU; Heath, F; Faergeman, O
      Functional characterization of two low density lipoprotein receptor gene mutations by fluorescence flow cytometric assessment of receptor activity instimulated human T-lymphocytes

      CLINICAL GENETICS
    84. Batalla, A; Alvarez, R; Reguero, JR; Hevia, S; Iglesias-Cubero, G; Alvarez, V; Cortina, A; Gonzalez, P; Celada, MM; Medina, A; Coto, E
      Synergistic effect between apolipoprotein E and angiotensinogen gene polymorphisms in the risk for early myocardial infarction

      CLINICAL CHEMISTRY
    85. Dufour, DR; Lott, JA; Nolte, FS; Gretch, DR; Koff, RS; Seeff, LB
      Diagnosis and monitoring of hepatic injury. II. Recommendations for use oflaboratory tests in screening, diagnosis, and monitoring

      CLINICAL CHEMISTRY
    86. Pirulli, D; Giordano, M; Puzzer, D; Crovella, S; Rigato, I; Tiribelli, C; Momigliano-Richiardi, P; Amoroso, A
      Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome

      CLINICAL CHEMISTRY
    87. Mori, A; Takagi, A; Ikeda, Y; Yamamoto, A
      Improved method for direct DNA sequencing of the human lipoprotein lipase gene using an auto DNA sequencer

      CLINICAL BIOCHEMISTRY
    88. Boyvat, A; Kundakci, N; Babikir, MOA; Gurgey, E
      Livedoid vasculopathy associated with heterozygous protein C deficiency

      BRITISH JOURNAL OF DERMATOLOGY
    89. Tsutsumi, K; Inoue, Y; Murase, T
      Effects of NO-1886, a lipoprotein lipase promoting agent, on homozygous and heterozygous watanabe heritable hyperlipidaemic rabbits

      ARZNEIMITTEL-FORSCHUNG-DRUG RESEARCH
    90. Dryja, TP
      Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    91. Yuan, B; Neuman, R; Duan, SH; Weber, JL; Kwok, PY; Saccone, NL; Wu, JS; Liu, KY; Schonfeld, G
      Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22

      AMERICAN JOURNAL OF HUMAN GENETICS
    92. Choi, Y; Ramnath, VR; Eaton, AS; Chen, A; Simon-Stoos, KL; Kleiner, DE; Erikson, J; Puck, JM
      Expression in transgenic mice of dominant interfering Fas mutations: A model for human autoimmune lymphoproliferative syndrome

      CLINICAL IMMUNOLOGY
    93. Thompson, GR
      Poor responders to statins: a potential target for stanol esters

      EUROPEAN HEART JOURNAL SUPPLEMENTS
    94. Sankaranarayanan, K
      Ionizing radiation and genetic risks - X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation genetics

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    95. Evans, HH; DeMarini, DM
      Ionizing radiation-induced mutagenesis: radiation studies in Neurospora predictive for results in mammalian cells

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    96. Shastry, BS; Hiraoka, M; Trese, DC; Trese, MT
      Norrie disease and exudative vitreoretinopathy in families with affected female carriers

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    97. al-Jandal, N; Farrar, GJ; Kiang, AS; Humphries, MM; Bannon, N; Findlay, JBC; Humphries, P; Kenna, PF
      A novel mutation without the rhodopsin gene (Thr-94-Ile) causing autosomaldominant congenital stationary night blindness

      HUMAN MUTATION
    98. Bambauer, R; Schneidewind, JM; Latza, R
      Apheresis technologies for prevention and regression of atherosclerosis: Clinical results

      ASAIO JOURNAL
    99. Stratakis, CA; Rennert, OM
      Congenital adrenal hyperplasia: Molecular genetics and alternative approaches to treatment

      CRITICAL REVIEWS IN CLINICAL LABORATORY SCIENCES
    100. Weatherall, D
      From genotype to phenotype: genetics and medical practice in the new millennium

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES


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Documento generato il 25/10/20 alle ore 15:39:19