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    1. Boardman, LA; Schmidt, S; Lindor, NM; Burgart, LJ; Cunningham, JM; Price-Troska, T; Snow, K; Ahlquist, DA; Thibodeau, SN
      A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair

      GENES CHROMOSOMES & CANCER
    2. Wang, LN; Bani-Hani, A; Montoya, DP; Roche, PC; Thibodeau, SN; Burgart, LJ; Roberts, LR
      HMLH1 and hMSH2 expression in human hepatocellular carcinoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    3. Wang, L; McDonnell, SK; Elkins, DA; Slager, SL; Christensen, E; Marks, AF; Cunningham, JM; Peterson, BJ; Jacobsen, SJ; Cerhan, JR; Blute, ML; Schaid, DJ; Thibodeau, SN
      Role of HPC2/ELAC2 in hereditary prostate cancer

      CANCER RESEARCH
    4. Aubry, MC; Halling, KC; Myers, JL; Tazelaar, HD; Yang, P; Thibodeau, SN
      DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lung

      CANCER
    5. Cunningham, JM; Kim, CY; Christensen, ER; Tester, DJ; Parc, Y; Burgart, LJ; Halling, KC; McDonnell, SK; Schaid, DJ; Vockley, CW; Kubly, V; Nelson, H; Michels, VV; Thibodeau, SN
      The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Schaid, DJ; McDonnell, SK; Thibodeau, SN
      Regression models for linkage heterogeneity applied to familial prostate cancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Bock, CH; Cunningham, JM; McDonnell, SK; Schaid, DJ; Peterson, BJ; Pavlic, RJ; Schroeder, JJ; Klein, J; French, AJ; Marks, A; Thibodeau, SN; Lange, EM; Cooney, KA
      Analysis of the prostate cancer-susceptibility locus HPC20 in 172 familiesaffected by prostate cancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    8. Yang, P; Cunningham, JM; Halling, KC; Lesnick, TG; Burgart, LJ; Wiegert, EM; Christensen, ER; Lindor, NM; Katzmann, JA; Thibodeau, SN
      Higher risk of mismatch repair-deficient colorectal cancer in alpha(1)-antitrypsin deficiency carriers and cigarette smokers

      MOLECULAR GENETICS AND METABOLISM
    9. Liu, WG; Dong, XY; Mai, M; Seelan, RS; Taniguchi, K; Krishnadath, KK; Halling, KC; Cunningham, JM; Boardman, LA; Qian, CP; Christensen, E; Schmidt, SJ; Roche, PC; Smith, DI; Thibodeau, SN
      Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling (vol 26, pg 146, 2000)

      NATURE GENETICS
    10. Liu, WG; Dong, XY; Mai, M; Seelan, RS; Taniguchi, K; Krishnadath, KK; Halling, KC; Cunningham, JM; Qian, CP; Christensen, E; Roche, PC; Smith, DI; Thibodeau, SN
      Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signalling

      NATURE GENETICS
    11. Boardman, LA; Couch, FJ; Burgart, LJ; Schwartz, D; Berry, R; McDonnell, SK; Schaid, DJ; Hartmann, LC; Schroeder, JJ; Stratakis, CA; Thibodeau, SN
      Genetic heterogeneity in Peutz-Jeghers syndrome

      HUMAN MUTATION
    12. Liu, WG; Mai, M; Yokomizo, A; Qian, CP; Tindall, DJ; Smith, DI; Thibodeau, SN
      Differential expression and allelotyping of the p73 gene in neuroblastoma

      INTERNATIONAL JOURNAL OF ONCOLOGY
    13. Urban, Z; Michels, VV; Thibodeau, SN; Davis, EC; Bonnefont, JP; Munnich, A; Eyskens, B; Gewillig, M; Devriendt, K; Boyd, CD
      Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay

      HUMAN GENETICS
    14. Brandhagen, DJ; Alvarez, W; Therneau, TM; Kruckeberg, KE; Thibodeau, SN; Ludwig, J; Porayko, MK
      Iron overload in cirrhosis - HFE genotypes and outcome after liver transplantation

      HEPATOLOGY
    15. Boardman, LA; Pittelkow, MR; Couch, FJ; Schaid, DJ; McDonnell, SK; Burgart, LJ; Ahlquist, DA; Carney, JA; Schwartz, DI; Thibodeau, SN; Hartmann, LC
      Association of Peutz-Jeghers-like mucocutaneous pigmentation with breast and gynecologic carcinomas in women

      MEDICINE
    16. Parc, YR; Halling, KC; Burgart, LJ; McDonnell, SK; Schaid, DJ; Thibodeau, SN; Halling, AC
      Microsatellite instability and hMLH1/hMSH2 expression in young endometrialcarcinoma patients: Associations with family history and histopathology

      INTERNATIONAL JOURNAL OF CANCER
    17. Ahlquist, DA; Skoletsky, JE; Boynton, KA; Harrington, JJ; Mahoney, DW; Pierceall, WE; Thibodeau, SN; Shuber, AP
      Colorectal cancer screening by detection of altered human DNA in stool: Feasibility of a multitarget assay panel

      GASTROENTEROLOGY
    18. Parc, YR; Halling, KC; Wang, L; Christensen, ER; Cunningham, JM; French, AJ; Burgart, LJ; Price-Troska, TL; Roche, PC; Thibodeau, SN
      hMSH6 alterations in patients with microsatellite instability-low colorectal cancer

      CANCER RESEARCH
    19. Sinclair, CS; Berry, R; Schaid, D; Thibodeau, SN; Couch, FJ
      BRCA1 and BRCA2 have a limited role in familial prostate cancer

      CANCER RESEARCH
    20. Berry, R; Schroeder, JJ; French, AJ; McDonnell, SK; Peterson, BJ; Cunningham, JM; Thibodeau, SN; Schaid, DJ
      Evidence for a prostate cancer-susceptibillty locus on chromosome 20

      AMERICAN JOURNAL OF HUMAN GENETICS
    21. Berry, R; Schaid, DJ; Smith, JR; French, AJ; Schroeder, JJ; McDonnell, SK; Peterson, BJ; Wang, ZY; Carpten, JD; Roberts, SG; Tester, DJ; Blute, ML; Trent, JM; Thibodeau, SN
      Linkage analyses at the chromosome 1 Loci 1q24-25 (HPC1), 1q42.2-43 (PCAP), and 1p36 (CAPB) in families with hereditary prostate cancer

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. Brandhagen, DJ; Fairbanks, VF; Baldus, WP; Smith, CI; Kruckeberg, KE; Schaid, DJ; Thibodeau, SN
      Prevalence and clinical significance of HFE gene mutations in patients with iron overload

      AMERICAN JOURNAL OF GASTROENTEROLOGY
    23. Cunningham, JM; Tester, DJ; Thibodeau, SN
      Mutation detection in colorectal cancers - Direct sequencing of DNA mismatch repair genes

      COLORECTAL CANCER: METHODS AND PROTOCOLS
    24. Yang, P; Wentzlaff, KA; Katzmann, JA; Marks, RS; Allen, MS; Lesnick, TG; Lindor, NM; Myers, JL; Wiegert, E; Midthun, DE; Thibodeau, SN; Krowka, MJ
      Alpha(1)-antitrypsin deficiency allele carriers among lung cancer patients

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    25. Endege, WO; Steinmann, KE; Boardman, LA; Thibodeau, SN; Schlegel, R
      Representative cDNA libraries and their utility in gene expression profiling

      BIOTECHNIQUES
    26. Urban, Z; Michels, VV; Thibodeau, SN; Donis-Keller, H; Csiszar, K; Boyd, CD
      Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts

      HUMAN GENETICS
    27. Tackels, D; Schwartz, CE; Thibodeau, SN; Michels, VV
      Refined gene localization for MRX7

      AMERICAN JOURNAL OF MEDICAL GENETICS
    28. Caselli, RJ; Graff-Radford, NR; Reiman, EM; Weaver, A; Osborne, D; Lucas, J; Uecker, A; Thibodeau, SN
      Preclinical memory decline in cognitively normal apolipoprotein E-epsilon 4 homozygotes

      NEUROLOGY
    29. Brandhagen, DJ; Fairbanks, VF; Batts, KP; Thibodeau, SN
      Update on hereditary hemochromatosis and the HFE gene

      MAYO CLINIC PROCEEDINGS
    30. Boland, CR; Thibodeau, SN; Hamilton, SR; Sidransky, D; Burt, RW; Meltzer, SJ; Rodriguez-Bigas, MA; Fodde, R; Ranzani, GN; Srivastava, S
      Correspondence re: C. R. Boland et al., a National Cancer Institute Workshop on Microsatellite Instability for Cancer Detection and Familial Predisposition: Development of International Criteria for the Determination of Microsatellite Instability in Colorectal Cancer. Cancer Res., 58 : 5248-5257, 1998. Reply

      CANCER RESEARCH
    31. Ameri, A; Fairbanks, VF; Yanik, GA; Mahdi, F; Thibodeau, SN; McCormick, DJ; Boxer, LA; McDonagh, KT
      Identification of the molecular genetic defect of patients with methemoglobin M Kankakee (M-Iwate), alpha 87 (F8) His -> Tyr: Evidence for an electrostatic model of alpha M hemoglobin assembly

      BLOOD
    32. Halling, KC; Harper, J; Moskaluk, CA; Thibodeau, SN; Petroni, GR; Yustein, AS; Tosi, P; Minacci, C; Roviello, F; Piva, P; Hamilton, SR; Jackson, CE; Powell, SM
      Origin of microsatellite instability in gastric cancer

      AMERICAN JOURNAL OF PATHOLOGY
    33. Halling, KC; French, AJ; McDonnell, SK; Burgart, LJ; Schaid, DJ; Peterson, BJ; Moon-Tasson, L; Mahoney, MR; Sargent, DJ; O'Connell, MJ; Witzig, TE; Farr, GH; Goldberg, RM; Thibodeau, SN
      Microsatellite instability and 8p allelic imbalance in stage B2 and C colorectal cancers

      JOURNAL OF THE NATIONAL CANCER INSTITUTE
    34. Cunningham, JM; Boardman, LA; Burgart, LJ; Thibodeau, SN
      Microsatellite instability

      MOLECULAR PATHOLOGY OF EARLY CANCER
    35. REIMAN EM; UECKER A; CASELLI RJ; LEWIS S; BANDY D; DELEON MJ; DESANTI S; CONVIT A; OSBORNE D; WEAVER A; THIBODEAU SN
      HIPPOCAMPAL VOLUMES IN COGNITIVELY NORMAL PERSONS AT GENETIC RISK FORALZHEIMERS-DISEASE

      Annals of neurology
    36. JACK CR; PETERSEN RC; XU YC; OBRIEN PC; WARING SC; TANGALOS EG; SMITH GE; IVNIK RJ; THIBODEAU SN; KOKMEN E
      HIPPOCAMPAL ATROPHY AND APOLIPOPROTEIN-E GENOTYPE ARE INDEPENDENTLY ASSOCIATED WITH ALZHEIMERS-DISEASE

      Annals of neurology
    37. HUTT PJ; PISCIOTTA AV; FAIRBANKS VF; THIBODEAU SN; GREEN MM
      DNA-SEQUENCE ANALYSIS PROVES HB-M MILWAUKEE-2 IS DUE TO BETA-GLOBIN GENE CODON-92 ((C)UNDER-BAR-AC-](T)UNDER-BAR-AC), THE PRESUMED MUTATIONOF HB-M-HYDE-PARK AND HB-M-AKITA

      Hemoglobin
    38. HOYER JD; WICK MJ; THIBODEAU SN; KECHTEIGER KS; COOK JD; FAIRBANKS VF
      HB SILVER-SPRINGS [BETA-131(H9)GLN-]HIS], A NEW HEMOGLOBIN-VARIANT FOUND IN 6 AFRICAN-AMERICANS

      Hemoglobin
    39. HOYER JD; WICK MJ; THIBODEAU SN; VIKER KA; CONNER R; FAIRBANKS VF
      HB TAK CONFIRMED BY DNA ANALYSIS - NOT EXPRESSED AS THALASSEMIA IN A HB TAK HB-E COMPOUND HETEROZYGOTE

      Hemoglobin
    40. LIU WG; SMITH DI; RECHTZIGEL KJ; THIBODEAU SN; JAMES CD
      DENATURING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY (DHPLC) USED IN THEDETECTION OF GERMLINE AND SOMATIC MUTATIONS

      Nucleic acids research
    41. O'Sullivan, DA; Torres, VE; Gabow, PA; Thibodeau, SN; King, BF; Bergstralh, EJ
      Cystic fibrosis and the phenotypic expression of autosomal dominant polycystic kidney disease

      AMERICAN JOURNAL OF KIDNEY DISEASES
    42. LINDOR NM; JALAL SM; VANDEWALKER TJ; CUNNINGHAM JM; DAHL RJ; THIBODEAU SN
      SEARCH FOR CHROMOSOME INSTABILITY IN LYMPHOCYTES WITH GERM-LINE MUTATIONS IN DNA MISMATCH REPAIR GENES

      Cancer genetics and cytogenetics
    43. OLSON TM; MICHELS VV; THIBODEAU SN; TAI YS; KEATING MT
      ACTIN MUTATIONS IN DILATED CARDIOMYOPATHY, A HERITABLE FORM OF HEART-FAILURE

      Science
    44. ACKERMAN MJ; SCHROEDER JJ; BERRY R; SCHAID DJ; PORTER CBJ; MICHELS VV; THIBODEAU SN
      A NOVEL MUTATION IN KVLQT1 IS THE MOLECULAR-BASIS OF INHERITED LONG QT SYNDROME IN A NEAR-DROWNING PATIENTS FAMILY

      Pediatric research
    45. BRANDHAGEN DJ; FAIRBANKS VF; BALDUS WP; SMITH CI; KRUCKEBERG KE; THIBODEAU SN
      PREVALENCE OF HFE GENE-MUTATIONS IN NORMAL BLOOD-DONORS AND IN PATIENTS WITH IRON OVERLOAD

      Gastroenterology
    46. BURGART LJ; BATTS KP; WANG L; ROCHE PC; TESTER DJ; THIBODEAU SN
      ADENOCARCINOMA INVOLVING COLONIC HYPERPLASTIC POLYPS IS ASSOCIATED WITH LOSS OF DNA-REPAIR ENZYME MLH-1

      Gastroenterology
    47. BURGART LJ; WANG L; ROCHE PC; TESTER DJ; THIBODEAU SN
      DNA MISMATCH REPAIR ENZYME (MLH1) STATUS OF ABERRANT CRYPT FOCI AND SMALL POLYPS ASSOCIATED WITH MLH1-NEGATIVE COLON ADENOCARCINOMA

      Gastroenterology
    48. KAMES WE; DUBOIS RN; SHATTUCKBRANDT R; BURGART LJ; TESTER DJ; THIBODEAU SN
      REDUCED COX-2 PROTEIN EXPRESSION IN HUMAN COLORECTAL-CANCER EXHIBITING DEFECTIVE MISMATCH REPAIR

      Gastroenterology
    49. THIBODEAU SN; FRENCH AJ; CUNNINGHAM JM; TESTER D; BURGART LJ; ROCHE PC; MCDONNELL SK; SCHAID DJ; VOCKLEY CW; MICHELS VV; FARR GH; OCONNELL MJ
      MICROSATELLITE INSTABILITY IN COLORECTAL-CANCER - DIFFERENT MUTATOR PHENOTYPES AND THE PRINCIPAL INVOLVEMENT OF HMLH1

      Cancer research
    50. CUNNINGHAM JM; CHRISTENSEN ER; TESTER DJ; KIM CY; ROCHE PC; BURGART LJ; THIBODEAU SN
      HYPERMETHYLATION OF THE HMLH1 PROMOTER IN COLON-CANCER WITH MICROSATELLITE INSTABILITY

      Cancer research
    51. Karnes, WE; Shattuck-Brandt, R; Burgart, LJ; DuBois, RN; Tester, DJ; Cunningham, JM; Kim, CY; McDonnell, SK; Schaid, DJ; Thibodeau, SN
      Reduced COX-2 protein in colorectal cancer with defective mismatch repair

      CANCER RESEARCH
    52. BOARDMAN LA; THIBODEAU SN; SCHAID DJ; LINDOR NM; MCDONNELL SK; BURGART LJ; AHLQUIST DA; PODRATZ KC; PITTELKOW M; HARTMANN LC
      INCREASED RISK FOR CANCER IN PATIENTS WITH THE PEUTZ-JEGHERS-SYNDROME

      Annals of internal medicine
    53. SCHAID DJ; MCDONNELL SK; BLUTE ML; THIBODEAU SN
      EVIDENCE FOR AUTOSOMAL-DOMINANT INHERITANCE OF PROSTATE-CANCER

      American journal of human genetics
    54. HALLING KC; BUFILL JA; COTTER M; ARTZ SA; CARPENTER AB; SCHAID D; HARTMANADAMS H; CHANG HH; BOUSTANY MM; FITHIAN L; JHIANG SM; THIBODEAU SN
      AGE-RELATED DISEASE PENETRANCE IN A LARGE MEDULLARY-THYROID CANCER FAMILY WITH A CODON-609 RET GENE MUTATION

      Molecular diagnosis
    55. KOCHHAR R; HALLING KC; MCDONNELL S; SCHAID DJ; FRENCH AJ; OCONNELL MJ; NAGORNEY DM; THIBODEAU SN
      ALLELIC IMBALANCE AND MICROSATELLITE INSTABILITY IN RESECTED DUKE D COLORECTAL-CANCER

      Diagnostic molecular pathology
    56. OSULLIVAN DA; TORRES VE; THIBODEAU SN; KING BF; OFFORD KP
      CYSTIC-FIBROSIS (CF) AND THE PHENOTYPIC-EXPRESSION OF AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) IN A FAMILY WITH COEXISTENT DISEASES

      Journal of the American Society of Nephrology
    57. MERRITT D; JONES RT; HEAD C; THIBODEAU SN; FAIRBANKS VF; STEINBERG MH; COLEMAN MB; RODGERS GP
      HB-SEAL-ROCK [(ALPHA-2)142-TERM-]GLU, CODON-142 (T)UNDER-BAR-AA-](G)UNDER-BAR-AA] - AN EXTENDED ALPHA-CHAIN VARIANT ASSOCIATED WITH ANEMIA,MICROCYTOSIS, AND ALPHA-THALASSEMIA-2 (-3.7-KB)

      Hemoglobin
    58. HUTT PJ; FAIRBANKS VF; THIBODEAU SN; GREEN MM; HOYER JD; BLOCK SH; DAY C; JONES RT; BARWICK RC
      HB T-CAMBODIA, A BETA-CHAIN VARIANT WITH THE MUTATIONS OF HB-E AND HBD-PUNJAB, CONFIRMED BY DNA ANALYSIS

      Hemoglobin
    59. PRUTHI RK; SCHAD C; THIBODEAU SN
      TRENDS IN MOLECULAR-GENETIC TESTING IN HEMOPHILIA-A (HA)

      Thrombosis and haemostasis
    60. BRANDHAGEN DJ; PORAYKO MK; MOYER TP; BALDUS WP; KRUCKEBERG KE; WIESNER RH; THIBODEAU SN
      GENETIC TESTING FOR HEMOCHROMATOSIS IN LIVER-TRANSPLANT RECIPIENTS WITH HEPATIC EXPLANT HEMOSIDEROSIS

      Hepatology
    61. LINDOR NM; VALDES MG; WICK M; THIBODEAU SN; JALAL S
      DE-NOVO 16P DELETION - ATR-16 SYNDROME

      American journal of medical genetics
    62. CASELLI RJ; GRAFFRADFORD NR; REIMAN EM; THIBODEAU SN; OSBORNE D; YUN LS; BANDY D
      CROSS-SECTIONAL AND LONGITUDINAL-STUDY OF PRESYMPTOMATIC ALZHEIMERS-DISEASE (AD) IN APOLIPOPROTEIN-E TYPE-4 (APOE-4) HOMOZYGOTES, HETEROZYGOTES, AND NONCARRIERS - NEUROPSYCHOLOGY COMPONENT

      Neurology
    63. HESHMATI HM; GHARIB H; KHOSLA S; ABULEBDEH HS; LINDOR NM; THIBODEAU SN
      GENETIC TESTING IN MEDULLARY-THYROID CARCINOMA SYNDROMES - MUTATION TYPES AND CLINICAL-SIGNIFICANCE

      Mayo Clinic proceedings
    64. HANSON CA; HOYER JD; THIBODEAU SN; KRUCKEBERG KE; LUST JA
      ABNORMAL HYPERMETHYLATION OF THE CALCITONIN-GENE - A NOVEL MARKER IN THE EVALUATION OF MYELODYSPLASIA (MDS)

      Laboratory investigation
    65. KRISHNA M; BURGART LJ; FRENCH AJ; MOONTASSON LL; MCDONNELL SK; SCHAID DJ; THIBODEAU SN
      PREDICTIVE VALUE OF HISTOPATHOLOGY FOR MUTATOR PHENOTYPE (MICROSATELLITE INSTABILITY) IN COLORECTAL-CARCINOMA

      Gastroenterology
    66. SIEGELMAN M; MOHABEER A; FAHEY TJ; TOMLINSON G; MAYAMBALA C; JAFARI S; NOLL WW; THIBODEAU SN; DAWSON DB
      RAPID, NONRADIOACTIVE SCREENING FOR MUTATIONS IN EXON-10, EXON-11, AND EXON-16 OF THE RET PROTOONCOGENE ASSOCIATED WITH INHERITED MEDULLARY-THYROID CARCINOMA

      Clinical chemistry
    67. BHUIYAN J; ROBERTS SG; THIBODEAU SN; OKANE DJ
      TELOMERASE ACTIVITIES IN BLADDER TISSUES, BLADDER WASHES AND IN URINEFROM PATIENTS WITH TRANSITIONAL-CELL CARCINOMA - A RAPID AND NONINVASIVE TECHNIQUE TO IDENTIFY BLADDER-CANCER

      Clinical chemistry
    68. TENNER KS; THIBODEAU SN; OKANE DJ
      A CHEMILUMINESCENCE (CL) ASSAY FOR DNA METHYLATION ANALYSIS IN THE DIAGNOSIS OF PRADER-WILLI-SYNDROME AND ANGELMAN-SYNDROME

      Clinical chemistry
    69. FAIRBANKS VF; THIBODEAU SN; GRANFORTUNA JM; LUBIN IM; SILVERMAN LM; ROHLFS EM
      IRON OVERLOADING IN BETA-THALASSEMIA TRAIT AND HEREDITARY SPHEROCYTOSIS - ANALYSIS OF C282Y AND H63D MUTATIONS

      Blood
    70. GREENBERG J; FAIRBANKS VF; HOYER J; THIBODEAU SN; FAIRFAX VA
      HEMOGLOBIN FAIRFAX, A TANDEM DUPLICATION OF BETA-90-94 INSERTED BETWEEN BETA-94-BETA-95 (PROVED BY DNA-SEQUENCE ANALYSIS) - A PREVIOUSLY UNDESCRIBED UNSTABLE HEMOGLOBIN-VARIANT ASSOCIATED WITH SEVERE HEMOLYTIC-ANEMIA AND STROKE DURING EARLY-CHILDHOOD

      Blood
    71. HOYER JD; WICK MJ; THIBODEAU SN; KECHTEIGER KS; COOK JD; FAIRBANKS VF
      HEMOGLOBIN SILVER-SPRINGS [BETA-131(H9) GLN-]HIS], A NEW HEMOGLOBIN-VARIANT FOUND IN 5 AFRICAN-AMERICANS

      Blood
    72. CUNNINGHAM JM; TESTER DJ; BURGART LJ; KIM CY; ROCHE PC; SCHAID DJ; NELSON H; THIBODEAU SN
      FREQUENCY OF ALTERED HMLH1 AND HMSH2 PROTEIN EXPRESSION IN UNSELECTEDCOLORECTAL-CANCER

      American journal of human genetics
    73. BOARDMAN LA; SCHROEDER JJ; MCDONNELL SK; BURGART LJ; HARTMANN LC; SCHAID DJ; THIBODEAU SN
      LINKAGE ANALYSIS IN PEUTZ-JEGHERS-SYNDROME TO CHROMOSOMAL ARM 19P

      American journal of human genetics
    74. LUBIN IM; FAIRBANKS V; THIBODEAU SN; HARRILL WS; GRANFORTUNA JM; SILVERMAN LM; ROHLFS EM
      HEREDITARY HEMOCHROMATOSIS IN ASSOCIATION WITH HETEROZYGOUS BETA-THALASSEMIA OR SPHEROCYTOSIS

      American journal of human genetics
    75. THIBODEAU SN; WANG Z; TESTER DJ; FRENCH AJ; SCHROEDER JJ; BISSONET AS; ROBERTS SG; BLUT ML; SCHAID DJ; SMITH JR; TRENT JM
      LINKAGE ANALYSIS AT THE HPC1 LOCUS IN HEREDITARY PROSTATE-CANCER FAMILIES

      American journal of human genetics
    76. LIM PC; TESTER D; CLIBY W; ZIESMER SC; ROCHE PC; HARTMANN L; THIBODEAU SN; PODRATZ KC; JENKINS RB
      ABSENCE OF MUTATIONS IN DNA MISMATCH REPAIR GENES IN SPORADIC ENDOMETRIAL TUMORS WITH MICROSATELLITE INSTABILITY

      Clinical cancer research
    77. MOSLEIN G; TESTER DJ; LINDOR NM; HONCHEL R; CUNNINGHAM JM; FRENCH AJ; HALLING KC; SCHWAB M; GORETZKI P; THIBODEAU SN
      MICROSATELLITE INSTABILITY AND MUTATION ANALYSIS OF HMSH2 AND HMLH1 IN PATIENTS WITH SPORADIC, FAMILIAL AND HEREDITARY COLORECTAL-CANCER

      Human molecular genetics
    78. URBAN Z; CSISZAR K; DONISKELLER H; THIBODEAU SN; BOYD CD
      ISOLATED SUPRAVALVULAR AORTIC-STENOSIS IS CHARACTERIZED BY A SPECTRUMOF MUTATIONS WITHIN THE ELASTIN GENE

      Matrix biology
    79. HUTT PJ; FAIRBANKS VF; GRIFFIN TC; THIBODEAU SN; GREEN MM; HOYER JD
      HB COOK [BETA-132(H10)LYS-]THR] - A NEW HEMOGLOBIN-VARIANT IN A SOUTHEAST-ASIAN FAMILY

      Hemoglobin
    80. HUTT PJ; DONALDSON MH; KHATRI J; FAIRBANKS VF; HOYER JD; THIBODEAU SN; MOXNESS MS; MCMORROW LE; GREEN MM; JONES RT
      HEMOGLOBIN-S HEMOGLOBIN-OSLER - A CASE WITH 3 BETA-GLOBIN CHAINS - DNA-SEQUENCE (AAT) PROVES THAT HB-OSLER IS BETA-145 TYR-]ASN

      American journal of hematology
    81. ENG C; CLAYTON D; SCHUFFENECKER I; LENOIR G; COTE G; GAGEL RF; VANAMSTEL HKP; LIPS CJM; NISHISHO I; TAKAI SI; MARSH DJ; ROBINSON BG; FRANKRAUE K; RAUE F; XUE FY; NOLL WW; ROMEI C; PACINI F; FINK M; NIEDERLE B; ZEDENIUS J; NORDENSKJOLD M; KOMMINOTH P; HENDY GN; GHARIB H; THIBODEAU SN; LACROIX A; FRILLING A; PONDER BAJ; MULLIGAN LM
      THE RELATIONSHIP BETWEEN SPECIFIC RET PROTOONCOGENE MUTATIONS AND DISEASE PHENOTYPE IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 - INTERNATIONAL RET MUTATION CONSORTIUM ANALYSIS

      JAMA, the journal of the American Medical Association
    82. REIMAN EM; CASELLI RJ; YUN LS; CHEN KW; BANDY D; MINOSHIMA S; THIBODEAU SN; OSBORNE D
      PRECLINICAL EVIDENCE OF ALZHEIMERS-DISEASE IN PERSONS HOMOZYGOUS FOR THE EPSILON-4 ALLELE FOR APOLIPOPROTEIN-E

      The New England journal of medicine
    83. WANG ZY; THIBODEAU SN
      A POLYMERASE CHAIN REACTION-BASED TEST FOR SPINAL AND BULBAR MUSCULAR-ATROPHY

      Mayo Clinic proceedings
    84. MOSLEIN G; HONCHEL R; SCHWAB M; GORETZKI P; ROHER HD; THIBODEAU SN
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/10/20 alle ore 07:47:34