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La ricerca find articoli where soggetti phrase all words 'mutation detection' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 353 riferimenti
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    1. Kwok, PY
      Methods for genotyping single nucleotide polymorphisms

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Clark, JM; Lee, SH; Kim, HJ; Yoon, KS; Zhang, AG
      DNA-based genotyping techniques for the detection of point mutations associated with insecticide resistance in Colorado potato beetle Leptinotarsa decemlineata

      PEST MANAGEMENT SCIENCE
    3. Pirrung, MC; Wang, LX; Montague-Smith, MP
      3 '-nitrophenylpropyloxycarbonyl (NPPOC) protecting groups for high-fidelity automated 5 ' -> 3 ' photochemical DNA synthesis

      ORGANIC LETTERS
    4. Marsh, DJ; Theodosopoulos, G; Howell, V; Richardson, AL; Benn, DE; Proos, AL; Eng, C; Robinson, BG
      Rapid mutation scanning of genes associated with familial cancer syndromesusing denaturing high-performance liquid chromatography

      NEOPLASIA
    5. Syvanen, AC
      Accessing genetic variation: Genotyping single nucleotide polymorphisms

      NATURE REVIEWS GENETICS
    6. Cooper, CS
      Applications of microarray technology in breast cancer research

      BREAST CANCER RESEARCH
    7. Oberacher, H; Oefner, PJ; Parson, W; Huber, CG
      On-line liquid chromatography mass spectrometry: A useful tool for the detection of DNA sequence variation

      ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
    8. Wilson, VL; Wade, KR; Yin, XQ; Albertini, RJ
      Temporal delineation of sequential HPRT mutations arising in vivo in a T-cell clone with a mutator phenotype

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    9. Jacobsen, NJO; Franks, EKE; Elvidge, G; Jones, I; McCandless, F; O'Donovan, MC; Owen, MJ; Craddock, N
      Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibilitygene for bipolar disorder

      MOLECULAR PSYCHIATRY
    10. Timur, AA; Gurgey, A; Aktuglu, G; Kavakli, K; Canatan, D; Olek, K; Caglayan, SH
      Molecular pathology of haemophilia A in Turkish patients: identification of 36 independent mutations

      HAEMOPHILIA
    11. 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
    12. Yenchitsomanus, P; Thanootarakul, P; Akkarapatumwong, V; Oranwiroon, S; Pung-Amritt, P; Veerakul, G; Mahasandana, C
      Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection

      HAEMOPHILIA
    13. Nakatani, K; Sando, S; Saito, I
      Scanning of guanine-guanine mismatches in DNA by synthetic ligands using surface plasmon resonance

      NATURE BIOTECHNOLOGY
    14. Yang, YP; Corley, N; Garcia-Heras, J
      Reverse dot-blot hybridization as an improved tool for the molecular diagnosis of point mutations in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency

      MOLECULAR DIAGNOSIS
    15. Ricevuto, E; Sobol, H; Stoppa-Lyonnet, D; Gulino, A; Marchetti, P; Ficorella, C; Martinotti, S; Meo, T; Tosi, M
      Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled amplicons

      CLINICAL CANCER RESEARCH
    16. Gelhaus, A; Scheding, A; Browne, E; Burchard, GD; Horstmann, RD
      Variability of the CD36 gene in West Africa

      HUMAN MUTATION
    17. Larsen, LA; Johnson, M; Brown, C; Christiansen, M; Frank-Hansen, R; Vuust, J; Andersen, PS
      Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis

      HUMAN MUTATION
    18. 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
    19. Geisler, JR; Hatterman-Zogg, MA; Rathe, JA; Lallas, TA; Kirby, P; Buller, RE
      Ovarian cancer BRCA1 mutation detection: Protein truncation test (PTT) outperforms single strand conformation polymorphism analysis (SSCP)

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

      HUMAN MUTATION
    21. 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
    22. Lodewyckx, L; Vandevyver, C; Vandervorst, C; Van Steenbergen, W; Raus, J; Michiels, L
      Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis

      HUMAN MUTATION
    23. Rannala, B; Bertorelle, G
      Using linked markers to infer the age of a mutation

      HUMAN MUTATION
    24. Hertz, JM; Juncker, I; Persson, U; Matthijs, G; Schmidtke, J; Petersen, MB; Kjeldsen, M; Gregersen, N
      Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome

      HUMAN MUTATION
    25. Jakubowska, A; Gorski, B; Byrski, T; Huzarski, T; Gronwald, J; Menkiszak, J; Cybulski, C; Debniak, T; Hadaczek, P; Scott, RJ; Lubinski, J
      Detection of germline mutations in the BRCA1 gene by RNA-based sequencing

      HUMAN MUTATION
    26. Feriotto, G; Ferlini, A; Ravani, A; Calzolari, E; Mischiati, C; Bianchi, N; Gambari, R
      Biosensor technology for real-time detection of the cystic fibrosis W1282Xmutation in CFTR

      HUMAN MUTATION
    27. Xiao, WZ; Oefner, PJ
      Denaturing high-performance liquid chromatography: A review

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

      HUMAN MUTATION
    29. Ye, F; Li, MS; Taylor, JD; Nguyen, Q; Colton, HM; Casey, WM; Wagner, M; Weiner, MP; Chen, JW
      Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification

      HUMAN MUTATION
    30. Nickerson, ML; Warren, MB; Zbar, B; Schmidt, LS
      Random mutagenesis-PCR to introduce alterations into defined DNA sequencesfor validation of SNP and mutation detection methods

      HUMAN MUTATION
    31. Edwards, SM; Kote-Jarai, Z; Hamoudi, R; Eeles, RA
      An improved high throughput heteroduplex mutation detection system for screening BRCA2 mutations - Fluorescent mutation detection (F-MD)

      HUMAN MUTATION
    32. Jakubowska, A; Gorski, B; Kurzawski, G; Debniak, T; Hadaczek, P; Cybulski, C; Kladny, J; Oszurek, O; Scott, RJ; Lubinski, J
      Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes

      HUMAN MUTATION
    33. Lothe, RA; Smith-Sorensen, B; Hektoen, M; Stenwig, AE; Mandahl, N; Saeter, G; Mertens, F
      Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors

      GENES CHROMOSOMES & CANCER
    34. 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
    35. Nakatani, K; Sando, S; Saito, I
      Improved selectivity for the binding of naphthyridine dimer to guanine-guanine mismatch

      BIOORGANIC & MEDICINAL CHEMISTRY
    36. Pirrung, MC; Worden, JD; Labriola, JP; Montague-Smith, MP; Weislo, LJ
      Solid-phase, single nucleotide primer extension of DNA/RNA hybrids by reverse transcriptases

      BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
    37. Kim, YS; Kang, DH; Kwon, DY; Park, WY; Kim, H; Lee, DS; Lim, CS; Han, JS; Kim, S; Lee, JS
      Uteroglobin gene polymorphisms affect the progression of immunoglobulin A nephropathy by modulating the level of uteroglobin expression

      PHARMACOGENETICS
    38. Forrest, SM; Knight, M; Akerman, BR; Cashman, JR; Treacy, EP
      A novel deletion in the flavin-containing monooxygenase gene (FMO3) in a Greek patient with trimethylaminuria

      PHARMACOGENETICS
    39. Verhoog, LC; van den Ouweland, AMW; Berns, E; van Veghel-Plandsoen, MM; van Staveren, IL; Wagner, A; Bartels, CCM; Tilanus-Linthorst, MMA; Devilee, P; Seynaeve, C; Halley, DJJ; Niermeijer, MF; Klijn, JGM; Meijers-Heijboer, H
      Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families

      EUROPEAN JOURNAL OF CANCER
    40. Schweitzer, B; Kingsmore, S
      Combining nucleic acid amplification and detection

      CURRENT OPINION IN BIOTECHNOLOGY
    41. Landegren, U
      Consulting the source code: prospects for gene-based medical diagnostics (Reprinted from Journal of Internal Medicine, vol 248, pg 271-276, 2000)

      JOURNAL OF INTERNAL MEDICINE
    42. Kapitanovic, S; Cacev, T; Spaventi, R; Pavelic, K
      Submerged gel electrophoresis on Spreadex gels - a new method for APC genemutation detection

      JOURNAL OF MOLECULAR MEDICINE-JMM
    43. Casana, P; Martinez, F; Haya, S; Espinos, C; Aznar, JA
      Association of the 3467C > T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease

      ANNALS OF HEMATOLOGY
    44. Heaton, MP; Grosse, WM; Kappes, SM; Keele, JW; Chitko-McKown, CG; Cundiff, LV; Braun, A; Little, DP; Laegreid, WW
      Estimation of DNA sequence diversity in bovine cytokine genes

      MAMMALIAN GENOME
    45. van den Heuvel, L; Op de Koul, K; Knots, E; Knoers, N; Monnens, L
      Autosomal recessive hypophosphataemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    46. Ringpfeil, E; Pulkkinen, L; Uitto, J
      Molecular genetics of pseudoxanthoma elasticum

      EXPERIMENTAL DERMATOLOGY
    47. 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
    48. DeFrancesco, L; Perkel, JM
      In search of genomic variation

      SCIENTIST
    49. Didenko, VV
      DNA probes using fluorescence resonance energy transfer (FRET): Designs and applications

      BIOTECHNIQUES
    50. Voisey, J; Hafner, GJ; Morris, CP; van Daal, A; Giffard, PM
      Interrogation of multimeric DNA amplification products by competitive primer extension using Bst DNA polymerase (large fragment)

      BIOTECHNIQUES
    51. Hamilton, SC; Farchaus, JW; Davis, MC
      DNA polymerases as engines for biotechnology

      BIOTECHNIQUES
    52. Xiao, W; Stern, D; Jain, M; Huber, CG; Oefner, PJ
      Multiplex capillary denaturing high-performance liquid chromatography withlaser-induced fluorescence detection

      BIOTECHNIQUES
    53. Hafner, GJ; Yang, IC; Wolter, LC; Stafford, MR; Giffard, PM
      Isothermal amplification and multimerization of DNA by bst DNA polymerase

      BIOTECHNIQUES
    54. Kristensen, VN; Kelefiotis, D; Kristensen, T; Borresen-Dale, AL
      High-throughput methods for detection of genetic variation

      BIOTECHNIQUES
    55. Ziemssen, F; Schnepf, R; Pfeiffer, A
      Single strand conformation polymorphism (SSCP) analysis in detection of point mutations: a technique and its limitations in the diagnostics of maturity onset diabetes in the young

      MEDIZINISCHE KLINIK
    56. Casana, P; Martinez, F; Haya, S; Tavares, A; Aznar, JA
      New mutations in exon 28 of the von Willebrand factor gene detected in patients with different types of von Willebrand's disease

      HAEMATOLOGICA
    57. Chen, JJZ; Yauk, CL; Hebert, C; Hebert, PDN
      Genetic variation in mitochondrial DNA of North American herring gulls, Larus argentatus

      JOURNAL OF GREAT LAKES RESEARCH
    58. Le Marechal, C; Audrezet, MP; Quere, I; Raguenes, O; Langonne, S; Ferec, C
      Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling

      HUMAN GENETICS
    59. Beaulieu, M; Larson, GP; Geller, L; Flanagan, SD; Krontiris, TG
      PCR candidate region mismatch scanning: adaptation to quantitative, high-throughput genotyping

      NUCLEIC ACIDS RESEARCH
    60. Broude, NE; Woodward, K; Cavallo, R; Cantor, CR; Englert, D
      DNA microarrays with stem-loop DNA probes: preparation and applications

      NUCLEIC ACIDS RESEARCH
    61. Gasser, RB; Chilton, NB
      Applications of single-strand conformation polymorphism (SSCP) to taxonomy, diagnosis, population genetics and molecular evolution of parasitic nematodes

      VETERINARY PARASITOLOGY
    62. Drabek, J
      A commented dictionary of techniques for genotyping

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

      ELECTROPHORESIS
    64. Razzaghi, H; Kamboh, MI
      A highly sensitive and nonradioactive mutation detection method based on vertical gradient temperature single-strand conformation polymorphism

      ELECTROPHORESIS
    65. Huber, CG; Premstaller, A; Wen, X; Oberacher, H; Bonn, GK; Oefner, PJ
      Mutation detection by capillary denaturing high-performance liquid chromatography using monolithic columns

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    66. Roberts, PS; Jozwiak, S; Kwiatkowski, DJ; Dabora, SL
      Denaturing high-performance liquid chromatography (DHPLC) is a highly sensitive, semi-automated method for identifying mutations in the TSC1 gene

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    67. Gross, E; Kiechle, M; Arnold, N
      Mutation analysis of p53 in ovarian rumors by DHPLC

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    68. Cotton, RGH; Bray, PJ
      Using CCM and DHPLC to detect mutations in the glucocorticoid receptor in atherosclerosis: a comparison

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    69. Pals, G; Young, C; Mao, HS; Worsham, MJ
      Detection of a single base substitution in a single cell using the LightCycler (TM)

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    70. Fleming, N; Maynard, J; Tzitzis, L; Sampson, JR; Cheadle, JP
      LD-PCR coupled to long-read direct sequencing: an approach for mutation detection in genes with compact genomic structures

      JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS
    71. Barker, DF; Denison, JC; Atkin, CL; Gregory, MC
      Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP

      AMERICAN JOURNAL OF MEDICAL GENETICS
    72. Feng, JN; Yan, J; Michaud, S; Craddock, N; Jones, IR; Cook, EH; Goldman, D; Heston, LL; Peltonen, L; Delisi, LE; Sommer, SS
      Scanning of estrogen receptor alpha (ER alpha) and thyroid hormone receptor alpha (TR alpha) genes in patients with psychiatric diseases: Four missense mutations identified in ER alpha gene

      AMERICAN JOURNAL OF MEDICAL GENETICS
    73. Chabas, A; Montfort, M; Martinez-Campos, M; Diaz, A; Coll, MJ; Grinberg, D; Vilageliu, L
      Mutation and haplotype analyses in 26 Spanish Sanfilippo syndrome type A patients: Possible single origin for 1091delC mutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Wittig, I; Augstein, P; Brown, GK; Fujii, T; Rotig, A; Rustin, P; Munnich, A; Seibel, P; Thorburn, D; Wissinger, B; Tamboom, K; Metspalu, A; Lamantea, E; Zeviani, M; Wehnert, MS
      Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain

      JOURNAL OF INHERITED METABOLIC DISEASE
    75. Peters, DJM; Breuning, MH
      Autosomal dominant polycystic kidney disease: modification of disease progression

      LANCET
    76. Bavykin, SG; Akowski, JP; Zakhariev, VM; Barsky, VE; Perov, AN; Mirzabekov, AD
      Portable system for microbial sample preparation and oligonucleotide microarray analysis

      APPLIED AND ENVIRONMENTAL MICROBIOLOGY
    77. Small, J; Call, DR; Brockman, FJ; Straub, TM; Chandler, DP
      Direct detection of 16S rRNA in soil extracts by using oligonucleotide microarrays

      APPLIED AND ENVIRONMENTAL MICROBIOLOGY
    78. Mathonnet, F; Peltier, JY; Roda, L; de Raucourt, E; D'Hailly, F; Tetegan, M; Catherine, N; Vinatier, I; de Mazancourt, P
      Three new cases of dysfibrinogenemia Poissy III, Saint-Germain I and Tahiti

      THROMBOSIS RESEARCH
    79. Jain, AN; Chin, K; Borresen-Dale, AL; Erikstein, BK; Lonning, PE; Kaaresen, R; Gray, JW
      Quantitative analysis of chromosomal CGH in human breast tumors associatescopy number abnormalities with p53 status and patient survival

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    80. Niu, TH; Seielstad, M; Zeng, X; Li, G; Apffel, A; Hahnenberger, K; Xu, XP
      Detection of novel ALAD gene polymorphisms using denaturing high-performance liquid chromatography

      HUMAN BIOLOGY
    81. Yakubovskaya, MG; Neschastnova, AA; Humphrey, KE; Babon, JJ; Popenko, VI; Smith, MJ; Lambrinakos, A; Lipatova, ZV; Dobrovolskaia, MA; Cappai, R; Masters, CL; Belitsky, GA; Cotton, RG
      Interaction of linear homologous DNA duplexes via Holliday junction formation

      EUROPEAN JOURNAL OF BIOCHEMISTRY
    82. Boutin, P; Vasseur, F; Samson, C; Wahl, C; Froguel, P
      Routine mutation screening of HNF-1 alpha and GCK genes in MODY diagnosis:How effective are the techniques of DHPLC and direct sequencing used in combination?

      DIABETOLOGIA
    83. Foy, CA; Parkes, HC
      Emerging homogeneous DNA-based technologies in the clinical laboratory

      CLINICAL CHEMISTRY
    84. Schaeffeler, E; Lang, T; Zanger, UM; Eichelbaum, M; Schwab, M
      High-throughput genotyping of thiopurine S-methyltransferase by denaturingHPLC

      CLINICAL CHEMISTRY
    85. Lam, CW; Hui, KN; Poon, PMK; Luk, NM; Yuen, YP; Tong, SF; Lai, CK; Chan, YW; Lo, KK
      Novel splicing mutation of the PPOX gene (IVS10+1G -> A) detected by denaturing high-performance liquid chromatography

      CLINICA CHIMICA ACTA
    86. Yang, AL; Festing, MFW
      A promoter function of the CCCGGG Sma I recognition sequence and its specific role in determining p53 status and identifying DNA damaging agents

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    87. Benoit, V; Steel, A; Torres, M; Lu, YY; Yang, HJ; Cooper, J
      Evaluation of three-dimensional microchannel glass biochips for multiplexed nucleic acid fluorescence hybridization assays

      ANALYTICAL CHEMISTRY
    88. Huber, M; Losert, D; Hiller, R; Harwanegg, C; Mueller, MW; Schmidt, WM
      Detection of single base alterations in genomic DNA by solid phase polymerase chain reaction on oligonucleotide microarrays

      ANALYTICAL BIOCHEMISTRY
    89. Wang, J; Kawde, AN
      Pencil-based renewable biosensor for label-free electrochemical detection of DNA hybridization

      ANALYTICA CHIMICA ACTA
    90. Thorstenson, YR; Shen, PD; Tusher, VG; Wayne, TL; Davis, RW; Chu, G; Oefner, PJ
      Global analysis of ATM polymorphism reveals significant functional constraint

      AMERICAN JOURNAL OF HUMAN GENETICS
    91. Berry, DA
      Role of population-based studies in assessing genetic cancer risk

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    92. Ben-Asher, E; Chalifa-Caspi, V; Horn-Saban, S; Avidan, N; Olender, Z; Adato, A; Glusman, G; Safran, M; Rubinstein, M; Lancet, D
      Harvesting the human genome: the Israeli perspective

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    93. Mir, KU; Southern, EM
      Sequence variation genes and genomic DNA: Methods for large-scale analysis

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    94. Tonisson, N; Kurg, A; Kaasik, K; Lohmussaar, E; Metspalu, A
      Unravelling genetic data by arrayed primer extension

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    95. Ren, JC
      High-throughput single-strand conformation polymorphism analysis by capillary electrophoresis

      JOURNAL OF CHROMATOGRAPHY B
    96. Burnouf, DY; Fuchs, RPP
      The early detection of frameshift mutations induced by a food-borne carcinogen in rats: a new tool for molecular epidemiology

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    97. Steinmetz, LM; Mindrinos, M; Oefner, PJ
      Combining genome sequences and new technologies for dissecting the genetics of complex phenotypes

      TRENDS IN PLANT SCIENCE
    98. Austin, J; Buckland, P; Cardno, AG; Williams, N; Spurlock, G; Hoogendoorn, B; Zammit, S; Jones, G; Sanders, R; Jones, L; McCarthy, G; Jones, S; Bray, NJ; McGuffin, P; Owen, MJ; O'Donovan, MC
      The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia

      MOLECULAR PSYCHIATRY
    99. Speight, G; Turic, D; Austin, J; Hoogendoorn, B; Cardno, AG; Jones, L; Murphy, KC; Sanders, R; McCarthy, G; Jones, I; McCandless, F; McGuffin, P; Craddock, N; Owen, MJ; Buckland, P; O'Donovan, MC
      Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder

      MOLECULAR PSYCHIATRY
    100. Wang, JJ; Bowman, CM; Wong, LJC
      A novel CFTR frame-shift mutation, 935delA, in two Hispanic cystic fibrosis patients

      MOLECULAR GENETICS AND METABOLISM


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Documento generato il 19/02/20 alle ore 18:20:15