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La ricerca find articoli where authors phrase all words ' CRAIG IW' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 43 riferimenti
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    1. Benjamin, D; Van Bakel, I; Craig, IW
      A novel expression based approach for assessing the inactivation status ofhuman X-linked genes

      EUROPEAN JOURNAL OF HUMAN GENETICS
    2. Koch, HG; McClay, J; Loh, EW; Higuchi, S; Zhao, JH; Sham, P; Ball, D; Craig, IW
      Allele association studies with SSR and SNP markers at known physical distances within a 1 Mb region embracing the ALDH2 locus in the Japanese, demonstrates linkage disequilibrium extending up to 400 kb

      HUMAN MOLECULAR GENETICS
    3. Craig, IW; McClay, J; Plomin, R; Freeman, B
      Chasing behaviour genes into the next millennium

      TRENDS IN BIOTECHNOLOGY
    4. Hill, L; Craig, IW; Asherson, P; Ball, D; Eley, T; Ninomiya, T; Fisher, PJ; Turic, D; McGuffin, P; Owen, MJ; Chorney, K; Chorney, MJ; Benbow, CP; Lubinski, D; Thompson, LA; Plomin, R
      DNA pooling and dense marker maps: a systematic search for genes for cognitive ability

      NEUROREPORT
    5. Tanaka, K; Fisher, SE; Craig, IW
      Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, Clcn5, implicated in X-linked hereditary nephrolithiasis

      GENOMICS
    6. Kenyon, JR; Craig, IW
      Analysis of the 5 ' regulatory region of the human Norrie's disease gene: evidence that a non-translated CT dinucleotide repeat in exon one has a role in controlling expression

      GENE
    7. Denney, RM; Koch, H; Craig, IW
      Association between monoamine oxidase A activity in human male shin fibroblasts and genotype of the MAOA promoter-associated variable number tandem repeat

      HUMAN GENETICS
    8. KOCH H; PARKES D; DAHLITZ M; CRAIG IW
      ANALYSIS OF THE MONOAMINE-OXIDASE GENES AND THE NORRIE DISEASE GENE LOCUS IN NARCOLEPSY

      American journal of medical genetics
    9. KOCH HG; DENNEY RM; ROSS M; CRAIG IW
      DETAILED ANALYSIS AND CLASSIFICATION OF A COMPLEX VNTR IN THE FIRST INTRON OF THE MONOAMINE-OXIDASE A GENE AND NEW SSR VARIANTS IN AND FLANKING THE MAOB GENE

      American journal of medical genetics
    10. WALKER JL; DIXON J; FENTON CR; HUNGERFORD J; LYNCH SA; STENHOUSES SAR; CHRISTIAN A; CRAIG IW
      2 NEW MUTATIONS IN EXON-3 OF THE NDP GENE - S73X AND S101F ASSOCIATEDWITH SEVERE AND LESS SEVERE OCULAR PHENOTYPE, RESPECTIVELY

      Human mutation
    11. LLOYD SE; GUNTHER W; PEARCE SHS; THOMSON A; BIANCHI ML; BOSIO M; CRAIG IW; FISHER SE; SCHEINMAN SJ; WRONG O; JENTSCH TJ; THAKKER RV
      CHARACTERIZATION OF RENAL CHLORIDE CHANNEL, CLCN5, MUTATIONS IN HYPERCALCIURIC NEPHROLITHIASIS (KIDNEY-STONES) DISORDERS

      Human molecular genetics
    12. FISHER SE; CICCODICOLA A; TANAKA K; CURCI A; DESICATO S; DURSO M; CRAIG IW
      SEQUENCE-BASED EXON PREDICTION AROUND THE SYNAPTOPHYSIN LOCUS REVEALSA GENE-RICH AREA CONTAINING NOVEL GENES IN HUMAN PROXIMAL XP

      Genomics
    13. BATRA RS; HATCHWELL E; RIDER S; BROWN R; BROWN GK; CRAIG IW
      LOCALIZATION OF HUMAN LIVER 6-PHOSPHOFRUCTO-2-KINASE FRUCTOSE-2,6-BISPHOSPHATASE (PFKFB1) WITHIN A YAC CONTIG IN XP11.21/

      Genomics
    14. SUAREZMERINO B; WALKER J; CRAIG IW
      DETAILED ANALYSIS OF A 2.5-MEGABASE GENOMIC REGION INCLUDING MAOA, MAOB, AND NDP GENES WHICH IS DELETED IN A CONTIGUOUS-GENE-SYNDROME WITH COMPLEX BEHAVIORAL DYSFUNCTION

      American journal of medical genetics
    15. BATTINELLI EM; BOYD Y; CRAIG IW; BREAKEFIELD XO; CHEN ZY
      CHARACTERIZATION AND MAPPING OF THE MOUSE NDP (NORRIE DISEASE) LOCUS (NDP)

      Mammalian genome
    16. LLOYD SE; PEARCE SHS; THOMSON A; BIANCHI ML; CRAIG IW; FISHER SE; SCHEINMAN SJ; WRONG OM; THAKKER RV
      MUTATIONS IN THE CHLORIDE CHANNEL GENE (CLCN5) ARE ASSOCIATED WITH HYPERCALCIURIC RICKETS AND NEPHROLITHIASIS

      Journal of bone and mineral research
    17. LLOYD SE; PEARCE SHS; FISHER SE; STEINMEYER K; SCHWAPPACH B; SCHEINMAN SJ; HARDING B; BOLINO A; DEVOTO M; GOODYER P; RIGDEN SPA; WRONG O; JENTSCH TJ; CRAIG IW; THAKKER RV
      A COMMON MOLECULAR-BASIS FOR 3 INHERITED KIDNEY-STONE DISEASES

      Nature
    18. BATRA RS; BROWN R; BROWN GK; CRAIG IW
      MOLECULAR-CLONING AND TISSUE-SPECIFIC EXPRESSION OF MOUSE KIDNEY 6-PHOSPHOFRUCTO-2-KINASE FRUCTOSE-2,6-BISPHOSPHATASE/

      FEBS letters
    19. SCHUBACK DE; CHEN ZY; CRAIG IW; BREAKEFIELD XO; SIMS KB
      MUTATIONS IN THE NORRIE DISEASE GENE

      Human mutation
    20. SCHEINMAN SJ; LLOYD SE; PEARCE SHS; HOPPES RR; FISHER SE; CRAIG IW; JENTSCH TJ; BUSHINSKY DA; THAKKER RV
      ROLE OF A VOLTAGE-GATED CHLORIDE-CHANNEL GENE CLC-5 IN HUMAN AND RAT HYPERCALCIURIA

      Journal of the American Society of Nephrology
    21. MATTHEWS PM; BENJAMIN D; VANBAKEL I; SQUIER MV; NICHOLSON LVB; SEWRY C; BARNES PRJ; HOPKIN J; BROWN R; HILTONJONES D; BOYD Y; KARPATI G; BROWN GK; CRAIG IW
      MUSCLE X-INACTIVATION PATTERNS AND DYSTROPHIN EXPRESSION IN DUCHENNE MUSCULAR-DYSTROPHY CARRIERS

      Neuromuscular disorders
    22. BLACK GCM; CRAIG IW; OOSTRA RJ; NORBY S; ROSENBERG T; MORTEN K; LABORDE A; POULTON J
      LEBER HEREDITARY OPTIC NEUROPATHY - IMPLICATIONS OF THE SEX-RATIO FORLINKAGE STUDIES IN FAMILIES WITH THE 3460 ND1 MUTATION

      Eye
    23. CHAND A; CLARK J; COOPER CS; CRAIG IW
      LONG-RANGE ORGANIZATION OF REITERATED SEQUENCES, INCLUDING THE SSX1 CDNA, AT THE OATL1 CLUSTER IN XP11.23

      Genomics
    24. FISHER SE; VANBAKEL I; LLOYD SE; PEARCE SHS; THAKKER RV; CRAIG IW
      CLONING AND CHARACTERIZATION OF CLCN5, THE HUMAN KIDNEY CHLORIDE CHANNEL GENE IMPLICATED IN DENT DISEASE (AN X-LINKED HEREDITARY NEPHROLITHIASIS)

      Genomics
    25. FISHER SE; HATCHWELL E; CHAND A; OCKENDEN N; MONACO AP; CRAIG IW
      CONSTRUCTION OF 2 YAC CONTIGS IN HUMAN XP11.23-P11.22, ONE ENCOMPASSING THE LOCI OATL1,GATA,TFE3, AND SYP, THE OTHER LINKING DXS255 TO DXS146

      Genomics
    26. BLAIR HJ; HO MF; MONACO AP; FISHER S; CRAIG IW; BOYD Y
      HIGH-RESOLUTION COMPARATIVE MAPPING OF THE PROXIMAL REGION OF THE MOUSE X-CHROMOSOME

      Genomics
    27. BLACK GCM; COLEMAN MP; CHEN ZY; NEMETH AH; DAVIES KE; CRAIG IW
      A BIDIRECTIONAL YAC WALK FROM THE NORRIE DISEASE (NDP) LOCUS

      Genomics
    28. LLOYD SE; PEARCE SIS; FISHER SE; HARDING B; SCHEINMAN SJ; GOODYER P; WRONG OM; CRAIG IW; THAKKER RV
      HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE

      Journal of bone and mineral research
    29. SCHEINMAN SJ; LLOYD SE; PEARCE SHS; FISHER SE; SALENGER PV; HOOPES RR; CRAIG IW; THAKKER RV
      ANALYSIS OF THE GENE ENCODING AN X-LINKED VOLTAGE-GATED CHLORIDE CHANNEL IN IDIOPATHIC HYPERCALIURIA

      Journal of bone and mineral research
    30. SHIPLEY JM; BIRDSALL S; CLARK J; CREW J; GILL S; LINEHAN M; GNARRA J; FISHER S; CRAIG IW; COOPER CS
      MAPPING THE X-CHROMOSOME BREAKPOINT IN 2 PAPILLARY RENAL-CELL CARCINOMA CELL-LINES WITH A T(X-1)(P11.2-Q21.2) AND THE FIRST REPORT OF A FEMALE CASE

      Cytogenetics and cell genetics
    31. HATCHWELL E; CRAIG IW
      FUNCTIONAL DISOMY OF A LOCUS (LOCI) IN XP AND HYPOMELANOSIS OF ITO

      Journal of Medical Genetics
    32. RACK KA; CHELLY J; GIBBONS RJ; RIDER S; BENJAMIN D; LAFRENIERE RG; OSCIER D; HENDRIKS RW; CRAIG IW; WILLARD HF; MONACO AP; BUCKLE VJ
      ABSENCE OF THE XIST GENE FROM LATE-REPLICATING ISODICENTRIC X-CHROMOSOMES IN LEUKEMIA

      Human molecular genetics
    33. FISHER SE; BLACK GCM; LLOYD SE; HATCHWELL E; WRONG O; THAKKER RV; CRAIG IW
      ISOLATION AND PARTIAL CHARACTERIZATION OF A CHLORIDE CHANNEL GENE WHICH IS EXPRESSED IN KIDNEY AND IS A CANDIDATE FOR DENTS DISEASE (AN X-LINKED HEREDITARY NEPHROLITHIASIS)

      Human molecular genetics
    34. REED V; RIDER S; MASLEN GL; HATCHWELL E; BLAIR HJ; UWECHUE IC; CRAIG IW; LAVAL SH; MONACO AP; BOYD Y
      A 2-MB YAC CONTIG ENCOMPASSING 3 LOCI (DXF34, DXS14, AND DXS390) THATLIE BETWEEN XP11.2 TRANSLOCATION BREAKPOINTS ASSOCIATED WITH INCONTINENTIA PIGMENTI TYPE-1

      Genomics
    35. SIMS KB; SCHUBACK D; CHEN ZY; CRAIG IW; BREAKEFIELD XO
      MUTATIONAL ANALYSIS IN THE NORRIE DISEASE GENE - AN EXPANDING PHENOTYPE

      Annals of neurology
    36. BLACK GM; CHEN ZY; COLEMAN M; DAVIES KE; CRAIG IW
      A BIDIRECTIONAL CHROMOSOME WALK FROM L1.28 (DXS7) EMBRACING 19 YAC CLONES

      Cytogenetics and cell genetics
    37. CRAIG IW
      ORGANIZATION OF THE HUMAN GENOME

      Journal of inherited metabolic disease
    38. CRAIG IW
      TRAVELING AROUND THE HUMAN GENOME - AN IN-SITU INVESTIGATION. - JORDAN,B

      Science
    39. CHEN ZY; BATTINELLI EM; FIELDER A; BUNDEY S; SIMS K; BREAKEFIELD XO; CRAIG IW
      A MUTATION IN THE NORRIE DISEASE GENE (NDP) ASSOCIATED WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY

      Nature genetics
    40. CHEN ZY; BATTINELLI EM; WOODRUFF G; YOUNG I; BREAKEFIELD XO; CRAIG IW
      CHARACTERIZATION OF A MUTATION WITHIN THE NDP GENE IN A FAMILY WITH AMANIFESTING FEMALE CARRIER

      Human molecular genetics
    41. CHEN ZY; BATTINELLI EM; HENDRIKS RW; POWELL JF; MIDDLETONPRICE H; SIMS KB; BREAKEFIELD XO; CRAIG IW
      NORRIE DISEASE GENE - CHARACTERIZATION OF DELETIONS AND POSSIBLE FUNCTION

      Genomics
    42. CHEN ZY; BATTINELLI EM; FIELDER A; BUNDEY S; SIMS K; BREAKEFIELD XO; CRAIG IW
      IDENTIFICATION OF A MUTATION IN THE NORRIE DISEASE GENE (NDP) IN AFFECTED MEMBERS OF A FAMILY WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY

      American journal of human genetics
    43. TUMER Z; TOMMERUP N; TONNESEN T; KREUDER J; CRAIG IW; HORN N
      MAPPING OF THE MENKES LOCUS TO XQ13.3 DISTAL TO THE X-INACTIVATION CENTER BY AN INTRACHROMOSOMAL INSERTION OF THE SEGMENT XQ13.3-Q21.2

      Human genetics


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Documento generato il 21/01/21 alle ore 06:16:35