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La ricerca find articoli where authors phrase all words 'HINNEY A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 43 riferimenti
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    1. 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
    2. Hamann, A; Brieske, C; Tafel, J; Buttron, P; Schwarzloh, B; Munzberg, H; Hinney, A; Mayer, H; Siegfried, W; Hebebrand, J; Greten, H; Algenstaedt, P; Ziegler, R
      Identification of a deletion variant in the gene encoding the human alpha(2A)-adrenergic receptor

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    3. Oeffner, F; Korn, T; Roth, H; Ziegler, A; Hinney, A; Goldschmidt, H; Siegfried, W; Hebebrand, J; Grzeschik, KH
      Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation

      INTERNATIONAL JOURNAL OF OBESITY
    4. Hebebrand, J; Sommerlad, C; Geller, F; Gorg, T; Hinney, A
      The genetics of obesity: practical implications

      INTERNATIONAL JOURNAL OF OBESITY
    5. Hamann, A; Disque, C; Munzberg, H; Tafel, J; Hinney, A; Mayer, H; Hebebrand, J; Ziegler, R
      Mutational screening of the human type II deiodinase gene

      HORMONE AND METABOLIC RESEARCH
    6. Oeffner, F; Bornholdt, D; Ziegler, A; Hinney, A; Gorg, T; Gerber, G; Goldschmidt, HP; Siegfried, W; Wright, A; Hebebrand, J; Grzeschik, KH
      Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents

      ACTA DIABETOLOGICA
    7. Hebebrand, J; Wulftange, H; Goerg, T; Ziegler, A; Hinney, A; Barth, N; Mayer, H; Remschmidt, H
      Epidemic obesity: are genetic factors involved via increased rates of assortative mating?

      INTERNATIONAL JOURNAL OF OBESITY
    8. Hinney, A; Ziegler, A; Oeffner, F; Wedewardt, C; Vogel, M; Wulftange, H; Geller, F; Stubing, K; Siegfried, W; Goldschmidt, HP; Remschmidt, H; Hebebrand, J
      Independent confirmation of a major locus for obesity on chromosome 10

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    9. Hinney, A; Ziegler, A; Oeffner, F; Wedewardt, C; Vogel, M; Wulftange, H; Geller, F; Stubing, K; Siegried, WG; Goldschmidt, HP; Remschmidt, H; Hebegrand, J
      Independent confirmation of a major locus for obesity on chromosome 10 (vol 85, pg 2962, 2000)

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    10. Hinney, A; Remschmidt, H; Hebebrand, J
      Candidate gene polymorphisms in eating disorders

      EUROPEAN JOURNAL OF PHARMACOLOGY
    11. Ziegler, A; Hebebrand, J; Gorg, T; Rosenkranz, K; Fichter, MM; Herpertz-Dahlmann, B; Remschmidt, H; Hinney, A
      Further lack of association between the 5-HT2A gene promoter polymorphism and susceptibility to eating disorders and a meta-analysis pertaining to anorexia nervosa

      MOLECULAR PSYCHIATRY
    12. Hamann, A; Munzberg, H; Buttron, P; Busing, B; Hinney, A; Mayer, H; Siegfried, W; Hebebrand, J; Greten, H
      Missense variants in the human peroxisome proliferator-activated receptor-gamma 2 gene in lean and obese subjects

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    13. Hinney, A; Herrmann, H; Lohr, T; Rosenkranz, K; Ziegler, A; Lehmkuhl, G; Poustka, F; Schmidt, MH; Mayer, H; Siegfried, W; Remschmidt, H; Hebebrand, J
      No evidence for an involvement of alleles of polymorphisms in the serotonin(1D beta and 7) receptor genes in obesity, underweight or anorexia nervosa

      INTERNATIONAL JOURNAL OF OBESITY
    14. Hinney, A; Schneider, J; Ziegler, A; Lehmkuhl, G; Poustka, F; Schmidt, MH; Mayer, H; Siegfried, W; Remschmidt, H; Hebebrand, J
      No evidence for involvement of polymorphisms of the dopamine D4 receptor gene in anorexia nervosa, underweight, and obesity

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Hebebrand, J; Ballauff, A; Hinney, A; Herpertz, S; Kopp, W; Wewetzer, C; Ziegler, A; Blum, WF; Remschmidt, H
      Body weight regulation in anorexia nervosa under special consideration of leptin secretion

      NERVENARZT
    16. Hinney, A; Schmidt, A; Nottebom, K; Heibult, O; Becker, I; Ziegler, A; Gerber, G; Sina, M; Gorg, T; Mayer, H; Siegfried, W; Fichter, M; Remschmidt, H; Hebebrand, J
      Several mutations in the melanocortin-4 receptor gene including a nonsenseand a frameshift mutation associated with dominantly inherited obesity in humans

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    17. Hamann, A; Busing, B; Munzberg, H; de Weerth, A; Hinney, A; Mayer, H; Siegfried, W; Hebebrand, J; Greten, H
      Missense variants in the human cholecystokinin type A receptor gene: No evidence for association with early-onset obesity

      HORMONE AND METABOLIC RESEARCH
    18. Sina, M; Hinney, A; Ziegler, A; Neupert, T; Mayer, H; Siegfried, W; Blum, WF; Remschmidt, H; Hebebrand, J
      Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    19. HINNEY A; BORNSCHEUER A; DEPENBUSCH M; MIERKE B; TOLLE A; MIDDEKE K; ZIEGLER A; ROTH H; GERBER G; ZAMZOW K; BALLAUFF A; HAMANN A; MAYER H; SIEGFRIED W; LEHMKUHL G; POUSTKA F; SCHMIDT MH; HERMANN H; HERPERTZDAHLMANN BM; FICHTER M; REMSCHMIDT H; HEBEBRAND J
      NO EVIDENCE FOR INVOLVEMENT OF THE LEPTIN GENE IN ANOREXIA-NERVOSA, BULIMIA-NERVOSA, UNDERWEIGHT OR EARLY-ONSET EXTREME OBESITY - IDENTIFICATION OF 2 NOVEL MUTATIONS IN THE CODING SEQUENCE AND A NOVEL POLYMORPHISM IN THE LEPTIN GENE LINKED UPSTREAM REGION

      Molecular psychiatry
    20. MUNZBERG H; TAFEL J; BUSING B; HINNEY A; ZIEGLER A; MAYER H; SIEGFRIED W; MATTHAEI S; GRETEN H; HEBEBRAND J; HAMANN A
      SCREENING FOR VARIABILITY IN THE CILIARY NEUROTROPHIC FACTOR (CNTF) GENE - NO EVIDENCE FOR ASSOCIATION WITH HUMAN OBESITY

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    21. Roth, H; Korn, T; Rosenkranz, K; Hinney, A; Ziegler, A; Kunz, J; Siegfried, W; Mayer, H; Hebebrand, J; Grzeschik, KH
      Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents

      HUMAN GENETICS
    22. HAMANN A; TAFEL J; BUSING B; MUNZBERG H; HINNEY A; MAYER H; SIEGFRIED W; RICQUIER D; GRETEN H; HEBEBRAND J; MATTHAEI S
      ANALYSIS OF THE UNCOUPLING PROTEIN-1 (UCP1) GENE IN OBESE AND LEAN SUBJECTS - IDENTIFICATION OF 4 AMINO-ACID VARIANTS

      International journal of obesity
    23. ROSENKRANZ K; HINNEY A; ZIEGLER A; VONPRITTWITZ S; BARTH N; ROTH H; MAYER H; SIEGFRIED W; LEHMKUHL G; POUSTKA F; SCHMIDT M; SCHAFER H; REMSCHMIDT H; HEBEBRAND J
      SCREENING FOR MUTATIONS IN THE NEUROPEPTIDE-Y Y5 RECEPTOR GENE IN COHORTS BELONGING TO DIFFERENT WEIGHT EXTREMES

      International journal of obesity
    24. HINNEY A; ROSENKRANZ K; ZIEGLER A; REMSCHMIDT H; HEBEBRAND J
      SCREENING OF CANDIDATE GENES IN PATIENTS WITH ANOREXIA-NERVOSA

      American journal of medical genetics
    25. HINNEY A; BECKER I; HEIBULT O; NOTTEBOM K; SCHMIDT A; ZIEGLER A; MAYER H; SIEGFRIED W; BLUM WF; REMSCHMIDT H; HEBEBRAND J
      SYSTEMATIC MUTATION SCREENING OF THE PROOPIOMELANOCORTIN GENE - IDENTIFICATION OF SEVERAL GENETIC-VARIANTS INCLUDING 3 DIFFERENT INSERTIONS, ONE NONSENSE AND 2 MISSENSE POINT MUTATIONS IN PROBANDS OF DIFFERENTWEIGHT EXTREMES

      The Journal of clinical endocrinology and metabolism
    26. Rosenkranz, K; Hinney, A; Ziegler, A; Hermann, H; Fichter, M; Mayer, H; Siegfried, W; Young, JK; Remschmidt, H; Hebebrand, J
      Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: Identification of several genetic variants

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    27. HEBEBRAND J; HINNEY A; ROTH H; BALLAUFF A; REMSCHMIDT H
      WILL LEPTIN PROVIDE AN INSIGHT INTO WEIGHT REGULATION OF PATIENTS WITH ANOREXIA-NERVOSA

      European eating disorders review
    28. ROTH H; HINNEY A; ZIEGLER A; BARTH N; GERBER G; STEIN K; BROMEL T; MAYER H; SIEGFRIED W; SCHAFER H; REMSCHMIDT H; GRZESCHIK KH; HEBEBRAND J
      FURTHER SUPPORT FOR LINKAGE OF EXTREME OBESITY TO THE OBESE GENE IN ASTUDY-GROUP OF OBESE CHILDREN AND ADOLESCENTS

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    29. HINNEY A; LENTES KU; ROSENKRANZ K; BARTH N; ROTH H; ZIEGLER A; HENNIGHAUSEN K; CONERS H; WURMSER H; JACOB K; ROMER G; WINNIKES U; MAYER H; HERZOG W; LEHMKUHL G; POUSTKA F; SCHMIDT MH; BLUM WF; PIRKE KM; SCHAFER H; GRZESCHIK KH; REMSCHMIDT H; HEBEBRAND J
      BETA(3)-ADRENERGIC-RECEPTOR ALLELE DISTRIBUTIONS IN CHILDREN, ADOLESCENTS AND YOUNG-ADULTS WITH OBESITY, UNDERWEIGHT OR ANOREXIA NERVOSA

      International journal of obesity
    30. HINNEY A; BORNSCHEUER A; DEPENBUSCH M; MIERKE B; TOLLE A; MAYER H; SIEGFRIED W; REMSCHMIDT H; HEBEBRAND J
      ABSENCE OF LEPTIN DEFICIENCY MUTATION IN EXTREMELY OBESE GERMAN CHILDREN AND ADOLESCENTS

      International journal of obesity
    31. LESCH KP; MEYER J; GLATZ K; FLUGGE G; HINNEY A; HEBEBRAND J; KLAUCK SM; POUSTKA A; POUSTKA F; BENGEL D; MOSSNER R; RIEDERER P; HEILS A
      THE 5-HT TRANSPORTER GENE-LINKED POLYMORPHIC REGION (5-HTTLPR) IN EVOLUTIONARY PERSPECTIVE - ALTERNATIVE BIALLELIC VARIATION IN RHESUS-MONKEYS

      Journal of neural transmission
    32. HINNEY A; ZIEGLER A; NOTHEN MM; REMSCHMIDT H; HEBEBRAND J
      5-HT2A RECEPTOR GENE POLYMORPHISMS, ANOREXIA-NERVOSA, AND OBESITY

      Lancet
    33. HINNEY A; BARTH N; ZIEGLER A; VONPRITTWITZ S; HAMANN A; HENNIGHAUSEN K; PIRKE KM; HEILS A; ROSENKRANZ K; ROTH H; CONERS H; MAYER H; HERZOG W; SIEGFRIED A; LEHMKUHL G; POUSTKA F; SCHMIDT MH; SCHAFER H; GRZESCHIK KH; LESCH KP; LENTES KU; REMSCHMIDT H; HEBEBRAND J
      SEROTONIN TRANSPORTER GENE-LINKED POLYMORPHIC REGION - ALLELE DISTRIBUTIONS IN RELATIONSHIP TO BODY-WEIGHT AND IN ANOREXIA-NERVOSA

      Life sciences
    34. LENTES KU; HINNEY A; ZIEGLER A; ROSENKRANZ K; WURMSER H; BARTH N; JACOB K; CONERS H; MAYER H; GRZESCHIK KH; SCHAFER H; REMSCHMIDT H; PIRKE KM; HEBEBRAND J
      EVALUATION OF A CYS23SER MUTATION WITHIN THE HUMAN 5-HT2C RECEPTOR GENE - NO EVIDENCE FOR AN ASSOCIATION OF THE MUTANT ALLELE WITH OBESITY OR UNDERWEIGHT IN CHILDREN, ADOLESCENTS AND YOUNG-ADULTS

      Life sciences
    35. SCHUCH B; HINNEY A; KNIPPER AJ; ENCZMANN J; KUBITZKY I; UHRBERG M; WERNET P
      DISTRIBUTION OF HLA CLASS-II DRB DQB AND DPB SUBTYPES WITH A POOL OF 506 POTENTIAL BONE-MARROW DONORS AND RECIPIENTS/

      Experimental hematology
    36. HAKENBERG P; ENCZMANN J; KNIPPER AJ; HINNEY A; WERNET P
      ANALYSIS OF THE DISTINGUISHABILITY OF ALLELIC COMBINATIONS OF DIRECTLY SEQUENCED HLA CLASS-I AND CLASS-II GENES

      Experimental hematology
    37. KUBITZKY I; ENCZMANN J; HINNEY A; SCHUCH B; AUER S; WERNET P
      PROSPECTIVE LARGE-SCALE DNA-BASED TYPING OF HLA CLASS-II GENES OF UNRELATED BONE-MARROW DONORS

      Experimental hematology
    38. HAKENBERG P; KIESEL U; ENCZMANN J; KNIPPER AJ; EPPINK R; HINNEY A; NAUMANN H; WERNET P
      CORD-BLOOD STEM-CELL TRANSPLANT SELECTION AS AN APPLICATION FOR AN UNIVERSAL PROGRAM FOR EASY IMPLEMENTING DIFFERENT IMMUNOGENETIC ALLOCATION RULES

      Experimental hematology
    39. DURR C; HINNEY A; LUEKENBACH C; RITTER H
      DETECTION OF 2 HYPERVARIABLE (ATTTT)N LOCI IN THE HUMAN GENOME

      Electrophoresis
    40. HINNEY A; DURR C; LUCKENBACH C; RITTER H
      TGGE AND HIEF - A COMPARISON OF 2 METHODS IN THE DETECTION OF CARRIERS OF THE Z-MUTATION OF THE ALPHA-1-ANTITRYPSIN GENE

      Human genetics
    41. ENCZMANN J; HINNEY A; KNIPPER A; SCHUCH B; WERNET P
      FINAL SELECTION OF UNRELATED BONE-MARROW DONORS BY NONRADIOACTIVE SEQUENCING OF HLA DRB1 3/4/5, DQB1, AND DPB1 ALLELES/

      Experimental hematology
    42. UHRBERG M; HINNEY A; ENCZMANN J; WERNET P
      ANALYSIS OF THE HLA-DR GENE LOCUS BY TEMPERATURE-GRADIENT GEL-ELECTROPHORESIS AND ITS APPLICATION FOR THE RAPID SELECTION OF UNRELATED BONE-MARROW DONORS

      Electrophoresis
    43. KNIPPER AJ; HINNEY A; SCHUCH B; ENCZMANN J; UHRBERG M; WERNET P
      SELECTION OF UNRELATED BONE-MARROW DONORS BY PCR-SSP TYPING AND SUBSEQUENT NONRADIOACTIVE SEQUENCE-BASED TYPING FOR HLA DRB1 3/4/5, DQB1, AND DPB1 ALLELES/

      Tissue antigens


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/08/20 alle ore 14:45:21