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La ricerca find articoli where authors phrase all words ' Sinke, RJ' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 33 riferimenti
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    1. van Voorn, B; Smit, HHG; Sinke, RJ; de Klerk, B
      Natural fibre reinforced sheet moulding compound

      COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
    2. Vink, T; Hinney, A; van Elburg, AA; van Goozen, SHM; Sandkuijl, LA; Sinke, RJ; Herpertz-Dahlmann, BM; Hebebrand, J; Remschmidt, H; van Engeland, H; Adan, RAH
      Association between an agouti-related protein gene polymorphism and anorexia nervosa

      MOLECULAR PSYCHIATRY
    3. van Alfen, N; Sinke, RJ; Zwarts, MJ; Gabreels-Festen, A; Praamstra, P; Kremer, BPH; Horstink, MWIM
      Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype

      ANNALS OF NEUROLOGY
    4. Giltay, JC; Ausems, MGEM; van Seumeren, I; Zewald, RA; Sinke, RJ; Faas, B; de Vroede, M
      Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic study

      EUROPEAN JOURNAL OF PEDIATRICS
    5. Schelhaas, HJ; Ippe, PF; Hageman, G; Sinke, RJ; van der Laan, EN; Beemer, FA
      Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia

      JOURNAL OF NEUROLOGY
    6. van de Warrenburg, BPC; Frenken, CWGM; Ausems, MGEM; Kleefstra, T; Sinke, RJ; Knoers, NVAM; Kremer, HPH
      Striking anticipation in spinocerebellar ataxia type 7: the infantile phenotype

      JOURNAL OF NEUROLOGY
    7. Sinke, RJ; Ippel, EF; Diepstraten, CM; Beemer, FA; Wokke, JHJ; van Hilten, BJ; Knoers, NVAM; van Amstel, HKP; Kremer, HPH
      Clinical and molecular correlations in spinocerebellar ataxia type 6 - A study of 24 Dutch families

      ARCHIVES OF NEUROLOGY
    8. Bull, LN; Juijn, JA; Liao, M; van Eijk, MJT; Sinke, RJ; Stricker, NL; DeYoung, JA; Carlton, VEH; Baharloo, S; Klomp, LWJ; Abukawa, D; Barton, DE; Bass, NM; Bourke, B; Drumm, B; Jankowska, I; Lovisetto, P; McQuaid, S; Pawlowska, J; Tazawa, Y; Villa, E; Tygstrup, N; Berger, R; Knisely, AS; Houwen, RHJ; Freimer, NB
      Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC (vol 104, pg 241, 1999)

      HUMAN GENETICS
    9. Bull, LN; Juijn, JA; Liao, M; van Eijk, MJT; Sinke, RJ; Stricker, NL; DeYoung, JA; Carlton, VEH; Baharloo, S; Klomp, LWJ; Abukawa, D; Barton, DE; Bass, NM; Bourke, B; Drumm, B; Jankowska, I; Lovisetto, P; McQuaid, S; Pawlowska, J; Tazawa, Y; Villa, E; Tygstrup, N; Berger, R; Knisely, AS; Houwen, RHJ; Freimer, NB
      Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 andBRIC

      HUMAN GENETICS
    10. IPPEL E; PHILIPPENS RMH; SINKE RJ; DIEPSTRATEN CM; HALLEY DJJ; TIJMENSEN ASLN; BEEMER FA; VANNIEUWENHUIZEN O
      GENOTYPE AND PHENOTYPE RELATIONSHIP IN PATIENTS WITH FRIEDREICHS-ATAXIA

      European journal of human genetics
    11. SINKE RJ; VANASSELDONK M; DEBRUIJN D; STRIJK JA; MERKX G; WEGHUIS DO; DEJONG B; OOSTERHUIS JW; VANKESSEL A
      TOWARDS THE ISOLATION OF A HUMAN-MALIGNANT EXTRAGONADAL GERM-CELL TUMOR-ASSOCIATED BREAKPOINT IN CHROMOSOME 11Q13

      APMIS. Acta pathologica, microbiologica et immunologica Scandinavica
    12. AUSEMS MGEM; VANDIGGELEN OP; SINKE RJ; REUSER AJJ; WOKKE JHJ
      GENOTYPE OF ADULT-ONSET GLYCOGEN-STORAGE-DISEASE TYPE-II IN ASYMPTOMATIC PATIENTS

      Neurology
    13. SJARIF DR; SINKE RJ; DURAN M; BEEMER FA; KLEIJER WJ; VANAMSTEL JKP; POLLTHE BT
      CLINICAL HETEROGENEITY AND NOVEL MUTATIONS IN THE GLYCEROL KINASE GENE IN 3 FAMILIES WITH ISOLATED GLYCEROL KINASE-DEFICIENCY

      Journal of Medical Genetics
    14. LANDSVATER RM; DEWIT MJ; PETERSON LF; SINKE RJ; VANKESSEL AG; LIPS CJM; HOPPENER JWM
      EXCLUSION OF THE NUCLEAR-FACTOR-KAPPA-B3 (REL-A) GENE AS CANDIDATE FOR THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN-1) GENE

      Biochemical and molecular medicine
    15. DEWIT MJ; LANDSVATER RM; SINKE RJ; VANKESSEL AG; LIPS CJM; HOPPENER JWM
      EXCLUSION OF THE PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE-C BETA-3(PLC BETA-3) GENE AS CANDIDATE FOR THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN-1) GENE

      Human genetics
    16. SINKE RJ; CARLTON VEH; JUIJN JA; DELHAAS T; BULL L; HENEGOUWEN GPV; VANHATTUM J; KELLER KM; SINAASAPPEL M; BIJLEVELD CMA; KNOL IE; VANAMSTEL HKP; PEARSON PL; BERGER R; FREIMER NB; HOUWEN RHJ
      BENIGN RECURRENT INTRAHEPATIC CHOLESTASIS (BRIC) - EVIDENCE OF GENETIC-HETEROGENEITY AND DELIMITATION OF THE BRIC LOCUS TO A 7-CM INTERVAL BETWEEN D18S69 AND D18S64

      Human genetics
    17. SINKE RJ; DIJKHUIZEN T; JANSSEN B; WEGHUIS DO; MERKX G; VANDENBERG E; SCHUURING E; MELONI AM; DEJONG B; VANKESSEL AG
      FINE MAPPING OF THE HUMAN RENAL ONCOCYTOMA-ASSOCIATED TRANSLOCATION (5-11)(Q35-Q13) BREAKPOINT

      Cancer genetics and cytogenetics
    18. VANAMSTEL JKP; SJARIF DR; DURAN M; KLEIJER WJ; BEEMER FA; SINKE RJ; POLL BT
      NOVEL MUTATIONS IN THE GLYCEROL KINASE GENE - MOLECULAR AND CLINICAL HETEROGENEITY IN ISOLATED GLYCEROL KINASE-DEFICIENCY

      American journal of human genetics
    19. VANECHTEN J; DEJONG B; SINKE RJ; WEGHUIS DO; SLEIJFER DT; OOSTERHUIS JW
      DEFINITION OF A NEW ENTITY OF MALIGNANT EXTRAGONADAL GERM-CELL TUMORS

      Genes, chromosomes & cancer
    20. HULSEBOS TJM; CEROSALETTI KM; FOURNIER REK; SINKE RJ; ROCCHI M; MARZELLA R; JENKINS NA; GILBERT DJ; COPELAND NG
      IDENTIFICATION OF THE HUMAN BETA-A2 CRYSTALLIN GENE (CRYBA2) - LOCALIZATION OF THE GENE ON HUMAN-CHROMOSOME-2 AND OF THE HOMOLOGOUS GENE ONMOUSE CHROMOSOME-1

      Genomics
    21. SINKE RJ; VANKESSEL AG
      LOCALIZATION OF THE HUMAN PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASEC-BETA(3), GENE (PLCB3) WITHIN CHROMOSOME BAND 11Q13

      Genomics
    22. WETERMAN MAJ; WILBRINK M; SINKE RJ; DEJONG B; VANKESSEL AG
      CONFINING THE BREAKPOINT REGION FOR THE PAPILLARY RENAL-CELL CARCINOMA-ASSOCIATED TRANSLOCATION T(X-1)(P11-Q21)

      Journal of cellular biochemistry
    23. BRAKENHOFF RH; GERRETSEN M; KNIPPELS EMC; VANDIJK M; VANESSEN H; WEGHUIS DO; SINKE RJ; SNOW GB; VANDONGEN GAMS
      THE HUMAN E48 ANTIGEN, HIGHLY HOMOLOGOUS TO THE MURINE LY-6 ANTIGEN THB, IS A GPI-ANCHORED MOLECULE APPARENTLY INVOLVED IN KERATINOCYTE CELL-CELL ADHESION

      The Journal of cell biology
    24. DEEN PMT; WEGHUIS DO; SINKE RJ; VANKESSEL AG; WIERINGA B; VANOS CH
      ASSIGNMENT OF THE HUMAN GENE FOR THE WATER CHANNEL OF RENAL COLLECTING DUCT AQUAPORIN-2 (AQP2) TO CHROMOSOME-12 REGION Q12-]Q13

      Cytogenetics and cell genetics
    25. DELEEUW B; SUIJKERBUIJK RF; WEGHUIS DO; SINKE RJ; VANKESSEL AG
      2 DISTINCT TRANSLOCATION BREAKPOINTS IN T(X-18)-POSITIVE SYNOVIAL SARCOMAS AND THEIR SUB-LOCALIZATION

      Cytogenetics and cell genetics
    26. SUIJKERBUIJK RF; SINKE RJ; WEGHUIS DEMO; ROQUE L; FORUS A; STELLINK F; SIEPMAN A; VANDEKAA C; SOARES J; VANKESSEL AG
      AMPLIFICATION OF CHROMOSOME SUBREGION 12P11.2-P12.1 IN A METASTASIS OF AN I(12P)-NEGATIVE SEMINOMA - RELATIONSHIP TO TUMOR PROGRESSION

      Cancer genetics and cytogenetics
    27. SINKE RJ; WEGHUIS DO; SUIJKERBUIJK RF; TANIGAMI A; NAKAMURA Y; LARSSON C; WEBER G; DEJONG B; OOSTERHUIS JW; MOLENAAR WM; VANKESSEL AG
      MOLECULAR CHARACTERIZATION OF A RECURRING COMPLEX CHROMOSOMAL TRANSLOCATION IN 2 HUMAN EXTRAGONADAL GERM-CELL TUMORS

      Cancer genetics and cytogenetics
    28. DELEEUW B; SUIJKERBUIJK RF; BALEMANS M; SINKE RJ; DEJONG B; MOLENAAR WM; MELONI AM; SANDBERG AA; GERAGHTY M; HOFKER M; ROPERS HH; VANKESSEL AG
      SUBLOCALIZATION OF THE SYNOVIAL SARCOMA-ASSOCIATED T(X-18) CHROMOSOMAL BREAKPOINT IN XP11.2 USING COSMID CLONING AND FLUORESCENCE INSITU HYBRIDIZATION

      Oncogene
    29. SINKE RJ; TANIGAMI A; NAKAMURA Y; VANKESSEL AG
      REVERSE MAPPING OF THE GENE ENCODING THE HUMAN FOS-RELATED ANTIGEN-1 (FRA-1) WITHIN CHROMOSOME BAND-11Q13

      Genomics
    30. SINKE RJ; DELEEUW B; JANSSEN HAP; WEGHUIS DO; SUIJKERBUIJK RF; MELONI AM; GILGENKRANTZ S; BERGER W; ROPERS HH; SANDBERG AA; VANKESSEL AG
      LOCALIZATION OF X-CHROMOSOME SHORT ARM MARKERS RELATIVE TO SYNOVIAL SARCOMA-ASSOCIATED AND RENAL ADENOCARCINOMA-ASSOCIATED TRANSLOCATION BREAKPOINTS

      Human genetics
    31. SUIJKERBUIJK RF; MELONI AM; SINKE RJ; DELEEUW B; WILBRINK M; JANSSEN HAP; GERAGHTY MT; MONACO AP; SANDBERG AA; VANKESSEL AG
      IDENTIFICATION OF A YEAST ARTIFICIAL CHROMOSOME THAT SPANS THE HUMAN PAPILLARY RENAL-CELL CARCINOMA-ASSOCIATED T(X1) BREAKPOINT IN XP11.2

      Cancer genetics and cytogenetics
    32. SUIJKERBUIJK RF; SINKE RJ; MELONI AM; PARRINGTON JM; VANECHTEN J; DEJONG B; OOSTERHUIS JW; SANDBERG AA; VANKESSEL AG
      OVERREPRESENTATION OF CHROMOSOME 12P SEQUENCES AND KARYOTYPIC EVOLUTION IN I(12P)-NEGATIVE TESTICULAR GERM-CELL TUMORS REVEALED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Cancer genetics and cytogenetics
    33. SCHULTZ D; MIKALA G; YATANI A; ENGLE DB; ILES DE; SEGERS B; SINKE RJ; WEGHUIS DO; KLOCKNER U; WAKAMORI M; WANG JJ; MELVIN D; VARADI G; SCHWARTZ A
      CLONING, CHROMOSOMAL LOCALIZATION, AND FUNCTIONAL EXPRESSION OF THE ALPHA-1-SUBUNIT OF THE L-TYPE VOLTAGE-DEPENDENT CALCIUM-CHANNEL FROM NORMAL HUMAN HEART

      Proceedings of the National Academy of Sciences of the United Statesof America


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Documento generato il 08/08/20 alle ore 14:43:56