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La ricerca find articoli where soggetti phrase all words 'molecular genetics' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 1284 riferimenti
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    1. Schneppenheim, R; Budde, U; Ruggeri, ZM
      A molecular approach to the classification of von Willebrand disease

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    2. Lowenberg, B
      Prognostic factors in acute myeloid leukaemia

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    3. Pei, Y
      A 'two-hit' model of cystogenesis in autosomal dominant polycystic kidney disease?

      TRENDS IN MOLECULAR MEDICINE
    4. Rougvie, AE
      Control of developmental timing in animals

      NATURE REVIEWS GENETICS
    5. Cronk, QCB
      Plant evolution and development in a post-genomic context

      NATURE REVIEWS GENETICS
    6. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    7. Lalouel, JM; Rohrwasser, A
      Development of genetic hypotheses in essential hypertension

      JOURNAL OF HUMAN GENETICS
    8. Schaefer, DG
      Gene targeting in Physcomitrella patens

      CURRENT OPINION IN PLANT BIOLOGY
    9. Kato, T
      The other, forgotten genome: mitochondrial DNA and mental disorders

      MOLECULAR PSYCHIATRY
    10. Theophilus, BDM; Enayat, MS; Williams, MD; Hill, FGH
      Site and type of mutations in the factor VIII gene in patients and carriers of haemophilia A

      HAEMOPHILIA
    11. Tang, S; Lai, KN
      Gene polymorphism in IgA nephropathy

      NEPHROLOGY
    12. Seeman, P; Mazanec, R; Ctvrteckova, M; Smilkova, D
      Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with centralconduction slowing

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    13. Takashima, H; Boerkoel, CF; Lupski, JR
      Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy

      GENETICS IN MEDICINE
    14. Lokki, ML; Laitinen, T
      Role of major histocompatibility complex class III genes in recurrent spontaneous abortions

      FRONTIERS IN BIOSCIENCE
    15. Highlander, SK
      Molecular genetic analysis of virulence in Mannheimia (Pasteurella) haemolytica

      FRONTIERS IN BIOSCIENCE
    16. Conesa, A; Punt, PJ; van Luijk, N; van den Hondel, CAMJJ
      The secretion pathway in filamentous fungi: A biotechnological view

      FUNGAL GENETICS AND BIOLOGY
    17. Zhang, ZJ; Butler, JD; Levin, SW; Wisniewski, KE; Brooks, SS; Mukherjee, AB
      Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood

      NATURE MEDICINE
    18. Srivastava, S; Verma, M; Henson, DE
      Biomarkers for early detection of colon cancer

      CLINICAL CANCER RESEARCH
    19. Vega, F; Medeiros, LJ
      Marginal-zone B-cell lymphoma of extranodal mucosa-associated lymphoid tissue type: Molecular genetics provides new insights into pathogenesis

      ADVANCES IN ANATOMIC PATHOLOGY
    20. Jameson, KA; Highnote, SM; Wasserman, LM
      Richer color experience in observers with multiple photopigment opsin genes

      PSYCHONOMIC BULLETIN & REVIEW
    21. Wirtzfeld, DA; Petrelli, NJ; Rodriguez-Bigas, MA
      Hamartomatous polyposis syndromes: Molecular genetics, neoplastic risk, and surveillance recommendations

      ANNALS OF SURGICAL ONCOLOGY
    22. 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
    23. Deltas, CC
      Mutations of the human polycystic kidney disease 2 (PKD2) gene

      HUMAN MUTATION
    24. Duponchel, C; Di Rocco, C; Cicardi, M; Tosi, M
      Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients

      HUMAN MUTATION
    25. Gale, C; Gerami-Nejad, M; McClellan, M; Vandoninck, S; Longtine, MS; Berman, J
      Candida albicans Int1p interacts with the septin ring in yeast and hyphal cells

      MOLECULAR BIOLOGY OF THE CELL
    26. Michels-Rautenstrauss, KG; Mardin, CY; Zenker, M; Jordan, N; Gusek-Schneider, GC; Rautenstrauss, BW
      Primary congenital glaucoma: Three case reports on novel mutations and combinations of mutations in the GLC3A (CYP1B1) gene

      JOURNAL OF GLAUCOMA
    27. Simonoff, E
      Gene-environment interplay in oppositional defiant and conduct disorder

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    28. Hsing, AW; Chen, C; Chokkalingam, AP; Gao, YT; Dightman, DA; Nguyen, HT; Deng, J; Cheng, JR; Sesterhenn, IA; Mostofi, FK; Stanczyk, FZ; Reichardt, JKV
      Polymorphic markers in the SRD5A2 gene and prostate cancer risk: A population-based case-control study

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    29. Bieche, I; Franc, B; Vidaud, D; Vidaud, M; Lidereau, R
      Analyses of MYC, ERBB2, and CCND1 genes in benign and malignant thyroid follicular cell tumors by real-time polymerase chain reaction

      THYROID
    30. Trapp, S; Croteau, R
      Defensive resin biosynthesis in conifers

      ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
    31. Hart, LA; Conron, M; du Bois, RM
      Sarcoidosis

      INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE
    32. Yagil, Y; Yagil, C
      Genetic models of hypertension in experimental animals

      EXPERIMENTAL NEPHROLOGY
    33. Bouba, I; Koptides, M; Mean, R; Costi, CE; Demetriou, K; Georgiou, I; Pierides, A; Siamopoulos, K; Deltas, CC
      Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families

      EUROPEAN JOURNAL OF HUMAN GENETICS
    34. Khadem, M; Rozas, J; Segarra, C; Aguade, M
      DNA variation at the rp49 gene region in Drosophila madeirensis and D-subobscura from Madeira: inferences about the origin of an insular endemic species

      JOURNAL OF EVOLUTIONARY BIOLOGY
    35. Davis, LM; Glenn, TC; Elsey, RM; Dessauer, HC; Sawyer, RH
      Multiple paternity and mating patterns in the American alligator, Alligator mississippiensis

      MOLECULAR ECOLOGY
    36. Eizirik, E; Kim, JH; Menotti-Raymond, M; Crawshaw, PG; O'Brien, SJ; Johnson, WE
      Phylogeography, population history and conservation genetics of jaguars (Panthera onca, Mammalia, Felidae)

      MOLECULAR ECOLOGY
    37. Fretland, AJ; Leff, MA; Doll, MA; Hein, DW
      Functional characterization of human N-acetyltransferase 2 (NAT2) single nucleotide polymorphisms

      PHARMACOGENETICS
    38. Dufau, ML; Tsai-Morris, CH; Tang, PZ; Khanum, A
      Regulation of steroidogenic enzymes and a novel testicular RNA helicase

      JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
    39. Aquadro, CF; DuMont, VB; Reed, FA
      Genome-wide variation in the human and fruitfly: a comparison

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    40. Charlesworth, D; Wright, SI
      Breeding systems and genome evolution

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    41. Fu, Y; Katsuya, T; Higaki, J; Asai, T; Fukuda, M; Takiuchi, S; Hatanaka, Y; Rakugi, H; Ogihara, T
      A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese

      JOURNAL OF HUMAN HYPERTENSION
    42. Pavelic, K; Gall-Troselj, K
      Recent advances in molecular genetics of breast cancer

      JOURNAL OF MOLECULAR MEDICINE-JMM
    43. Radner, H; Katenkamp, D; Reifenberger, G; Deckert, M; Pietsch, T; Wiestler, OD
      New developments in the pathology of skull base tumors

      VIRCHOWS ARCHIV-AN INTERNATIONAL JOURNAL OF PATHOLOGY
    44. McGleenan, T; Wiesing, U
      Insurance and genetics - Options to prevent undesirable consequences

      GESUNDHEITSWESEN
    45. Nakanishi, K; Sweeney, WE; Avner, ED; Murcia, NS
      Expression of the orpk disease gene during kidney development and maturation

      PEDIATRIC NEPHROLOGY
    46. Plantaz, D
      Neuroblastoma, one century after Pepper: Which genes?

      ARCHIVES DE PEDIATRIE
    47. Shinozaki-Kuwahara, N; Hayakawa, M; Shiroza, T; Abiko, Y; Fukushima, K
      Purification and characterization of an oligo-isomaltosaccharide synthase from a Streptococcus sobrinus glucosyltransferase-I deficient mutant.

      BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
    48. Zimonjic, DB; Keck-Waggoner, C; Popescu, NC
      Novel genomic imbalances and chromosome translocations involving c-myc gene in Burkitt's lymphoma

      LEUKEMIA
    49. Yin, TM; Huang, MR; Wang, MX; Zhu, LH; Zeng, ZB; Wu, RL
      Preliminary interspecific genetic maps of the Populus genome constructed from RAPD markers

      GENOME
    50. Li, CX; Yeh, FC
      Construction of a framework map in Pinus contorta subsp latifolia using random amplified polymorphic DNA markers

      GENOME
    51. Disse-Nicodeme, S; Corvol, P; Jeunemaitre, X; Achard, JM
      Two genes involved in human familial hypertension

      M S-MEDECINE SCIENCES
    52. Schachter, F; Foulon, M; Poulain, M
      Color vision anomalies and the genetics of aging.

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    53. Guinand, B; Durand, JD; Laroche, J
      Identifying main evolutionary mechanisms shaping genetic variation of Leuciscus cephalus L. 1758 (Cyprinidae) in Western Greece: discordance between methods

      COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES
    54. Tauber, E; Kyriacou, BP
      Insect photoperiodism and circadian clocks: Models and mechanisms

      JOURNAL OF BIOLOGICAL RHYTHMS
    55. Rubin, BP; Dal Cin, P
      The genetics of lipomatous tumors

      SEMINARS IN DIAGNOSTIC PATHOLOGY
    56. Bielawski, JP; Yang, ZH
      Positive and negative selection in the DAZ gene family

      MOLECULAR BIOLOGY AND EVOLUTION
    57. Andolfatto, P
      Contrasting patterns of X-linked and autosomal nucleotide variation in Drosophila melanogaster and Drosophila simulans

      MOLECULAR BIOLOGY AND EVOLUTION
    58. Przeworski, M; Wall, JD; Andolfatto, P
      Recombination and the frequency spectrum in Drosophila melanogaster and Drosophila simulans

      MOLECULAR BIOLOGY AND EVOLUTION
    59. Aguade, M
      Nucleotide sequence variation at two genes of the phenylpropanoid pathway,the FAH1 and F3H genes, in Arabidopsis thaliana

      MOLECULAR BIOLOGY AND EVOLUTION
    60. Dinus, RJ; Payne, P; Sewell, NM; Chiang, VL; Tuskan, GA
      Genetic modification of short rotation popular wood: Properties for ethanol fuel and fiber productions

      CRITICAL REVIEWS IN PLANT SCIENCES
    61. Jang, KL; Vernon, PA; Livesley, WJ
      Behavioural-genetic perspectives on personality function

      CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE
    62. Johnson, TE; de Castro, E; de Castro, SH; Cypser, J; Henderson, S; Tedesco, P
      Relationship between increased longevity and stress resistance as assessedthrough gerontogene mutations in Caenorhabditis elegans

      EXPERIMENTAL GERONTOLOGY
    63. Petursdottir, V; Moslemi, AR; Persson, M; Nordborg, E; Nordborg, C
      Estrogen receptor alpha in giant cell arteritis: A molecular genetic study

      CLINICAL AND EXPERIMENTAL RHEUMATOLOGY
    64. Veneselli, E; Biancheri, R; Buoni, S; Fois, A
      Clinical and EEG findings in 18 cases of late infantile neuronal ceroid lipofuscinosis

      BRAIN & DEVELOPMENT
    65. Kawamura, S; Hirai, M; Takenaka, O; Radlwimmer, FB; Yokoyama, S
      Genomic and spectral analyses of long to middle Wavelength-sensitive visual pigments of common marmoset (Callithrix jacchus)

      GENE
    66. Comabella, M; Waye, JS; Raguer, N; Eng, B; Dominguez, C; Navarro, C; Borras, C; Krivit, W; Montalban, X
      Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family

      ANNALS OF NEUROLOGY
    67. Morris, M; Means, S; Oliverio, MI; Coffman, TM
      Enhanced central response to dehydration in mice lacking angiotensin AT(1a) receptors

      AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
    68. Hayashi, T; Yamaguchi, T; Kitahara, K; Sharpe, LT; Jagle, H; Yamade, S; Ueyama, H; Motulsky, AG; Deeb, SS
      The importance of gene order in expression of the red and green visual pigment genes and in color vision

      COLOR RESEARCH AND APPLICATION
    69. Yamade, S; Hayashi, S; Ueyama, H; Tanabe, S; Hukami, K; Ichikawa, K; Tachibana, M
      Red-green pigment gene analysis as a clinical diagnostic tool

      COLOR RESEARCH AND APPLICATION
    70. Bollinger, K; Bialozynski, C; Neitz, J; Neitz, M
      The importance of deleterious mutations of M pigment genes as a cause of color vision defects

      COLOR RESEARCH AND APPLICATION
    71. Carroll, J; Neitz, M; Neitz, J
      Testing hypotheses about visual pigments underlying deutan color vision

      COLOR RESEARCH AND APPLICATION
    72. Jacobs, GH; Williams, GA
      The prevalence of defective color vision in Old World monkeys and apes

      COLOR RESEARCH AND APPLICATION
    73. Neitz, M; Neitz, J
      A new mass screening test for color-vision deficiencies in children

      COLOR RESEARCH AND APPLICATION
    74. Beesley, CE; Meaney, CA; Greenland, G; Adams, V; Vellodi, A; Young, EP; Winchester, BG
      Mutational analysis of 85 mucopolysaccharidosis type I families: frequencyof known mutations, identification of 17 novel mutations and in vitro expression of missense mutations

      HUMAN GENETICS
    75. Takenaga, M; Horinouchi, K; Shirieda, K; Fukudome, T; Fujimoto, T
      A novel nonsense mutation in the antithrombin III gene (Ser365 to stop) causing deep and mesenteric venous thromboses

      THROMBOSIS AND HAEMOSTASIS
    76. Lang-Muritano, M; Biason-Lauber, A; Gitzelmann, C; Belville, C; Picard, Y; Schoenle, EJ
      A novel mutation in the anti-mullerian hormone gene as cause of persistentmullerian duct syndrome

      EUROPEAN JOURNAL OF PEDIATRICS
    77. Benjafield, AV; Lin, RCY; Dalziel, B; Gosby, AK; Caterson, ID; Morris, BJ
      G-protein ss 3 subunit gene splice variant in obesity and overweight

      INTERNATIONAL JOURNAL OF OBESITY
    78. Mowry, BJ; Nancarrow, DJ
      Molecular genetics of schizophrenia

      CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY
    79. Rawlings, DE
      The molecular genetics of Thiobacillus ferrooxidans and other mesophilic, acidophilic, chemolithotrophic, iron- or sulfur-oxidizing bacteria

      HYDROMETALLURGY
    80. Loke, KY; Lee, YS; Lee, WWR; Poh, LKS
      Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore

      HORMONE RESEARCH
    81. Thierfelder, L
      Genetic diagnosis in cardiovascular medicine

      ZEITSCHRIFT FUR KARDIOLOGIE
    82. Smit, JWA; Van Zelderen-Bhola, S; Merx, R; De Leeuw, W; Wessels, H; Vink, R; Morreau, H
      A novel chromosomal translocation t(3;5)(q12;p15.3) and loss of heterozygosity on chromosome 22 in a multifocal follicular variant of papillary thyroid carcinoma presenting with skin metastases

      CLINICAL ENDOCRINOLOGY
    83. Todd, R; Donoff, RB; Kim, Y; Wong, DTW
      From the chromosome to DNA: Restriction fragment length polymorphism analysis and its clinical application

      JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY
    84. Verma, A; Bradley, WG
      Atypical motor neuron disease and related motor syndromes

      SEMINARS IN NEUROLOGY
    85. Mishra, RK; Mihaly, J; Barges, S; Spierer, A; Karch, F; Hagstrom, K; Schweinsberg, SE; Schedl, P
      The iab-7 polycomb response element maps to a nucleosome-free region of chromatin and requires both GAGA and pleiohomeotic for silencing activity

      MOLECULAR AND CELLULAR BIOLOGY
    86. Lim, CJ; Spiegelman, GB; Weeks, G
      RasC is required for optimal activation of adenylyl cyclase and Akt/PKB during aggregation

      EMBO JOURNAL
    87. Formosa, T; Eriksson, P; Wittmeyer, J; Ginn, J; Yu, YX; Stillman, DJ
      Spt16-Pob3 and the HMG protein Nhp6 combine to form the nucleosome-bindingfactor SPN

      EMBO JOURNAL
    88. Dale, B
      The sedimentary record of dinoflagellate cysts: looking back into the future of phytoplankton blooms

      SCIENTIA MARINA
    89. Bain, BJ
      The morphological, immunophenotypic, cytogenetic, molecular genetic (MIC-M) classification of acute leukaemia

      EXPERIMENTAL ONCOLOGY
    90. Allayee, H; de Bruin, TWA; Dominguez, KM; Cheng, LSC; Ipp, E; Cantor, RM; Krass, KL; Keulen, ETP; Aouizerat, BE; Lusis, AJ; Rotter, JI
      Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p

      HYPERTENSION
    91. Danziger, RS
      Hypertension in an anthropological and evolutionary paradigm

      HYPERTENSION
    92. Martinez, A; Soberon-Chavez, G
      Characterization of the lipA gene encoding the major lipase from Pseudomonas aeruginosa strain IGB83

      APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
    93. Werner, M; Becker, KF; Keller, G; Hofler, H
      Gastric adenocarcinoma: pathomorphology and molecular pathology

      JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
    94. Kaplan, JM; Pigliucci, M
      Genes 'for' phenotypes: A modern history view

      BIOLOGY & PHILOSOPHY
    95. Dessen, P; Zagulski, M; Gromadka, R; Plattner, H; Kissmehl, R; Meyer, E; Betermier, M; Schultz, JE; Linder, JU; Pearlman, RE; Kung, C; Forney, J; Satir, BH; Van Houten, JL; Keller, AM; Froissard, M; Sperling, L; Cohen, J
      Paramecium genome survey: a pilot project

      TRENDS IN GENETICS
    96. Araz, M; Yilmaz, N; Gungor, K; Okan, V; Kepekci, Y; Aynacioglu, AS
      Angiotensin-converting enzyme gene polymorphism and microvascular complications in Turkish type 2 diabetic patients

      DIABETES RESEARCH AND CLINICAL PRACTICE
    97. Kato, T
      Molecular genetics of bipolar disorder

      NEUROSCIENCE RESEARCH
    98. Doevendans, PA; Jukema, W; Spiering, W; Defesche, JC; Kastelein, JJP
      Molecular genetics and gene expression in atherosclerosis

      INTERNATIONAL JOURNAL OF CARDIOLOGY
    99. Ramsay, RR; Gandour, RD; van der Leij, FR
      Molecular enzymology of carnitine transfer and transport

      BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
    100. Nadol, JB; Merchant, SN
      Histopathology and molecular genetics of hearing loss in the human

      INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY


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Documento generato il 10/12/19 alle ore 01:27:50