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La ricerca find articoli where authors phrase all words ' COGAN JD' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 15 riferimenti
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    1. Pernasetti, F; Toledo, SPA; Vasilyev, VV; Hayashida, CY; Cogan, JD; Ferrari, C; Lourenco, DM; Mellon, PL
      Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the Prophet of Pit-1 gene

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    2. Cogan, JD; Phillips, JA
      Molecular defects in the growth hormone axis

      MOLECULAR AND CELLULAR PEDIATRIC ENDOCRINOLOGY
    3. WU W; COGAN JD; PFAFFLE RW; DASEN JS; FRISCH H; OCONNELL SM; FLYNN SE; BROWN MR; MULLIS PE; PARKS JS; PHILLIPS JA; ROSENFELD MG
      MUTATIONS IN PROP1 CAUSE FAMILIAL COMBINED PITUITARY-HORMONE DEFICIENCY

      Nature genetics
    4. ARNHOLD IJP; OSORIO MGF; OLIVEIRA SB; ESTEFAN V; KAMIJO T; KRISHNAMANI MRS; COGAN JD; PHILLIPS JA; MENDONCA BB
      CLINICAL AND MOLECULAR CHARACTERIZATION OF BRAZILIAN PATIENTS WITH GROWTH-HORMONE GENE DELETIONS

      Brazilian journal of medical and biological research
    5. COGAN JD; WU W; PHILLIPS JA; ARNHOLD IJP; AGAPITO A; FOFANOVA OV; OSORIO MGF; BIRCAN I; MORENO A; MENDONCA BB
      THE PROP1 2-BASE PAIR DELETION IS A COMMON-CAUSE OF COMBINED PITUITARY-HORMONE DEFICIENCY

      The Journal of clinical endocrinology and metabolism
    6. COGAN JD; PRINCE MA; LEKHAKULA S; BUNDEY S; FUTRAKUL A; MCCARTHY EMS; PHILLIPS JA
      A NOVEL MECHANISM OF ABERRANT PRE-MESSENGER-RNA SPLICING IN HUMANS

      Human molecular genetics
    7. MIYATA I; COGAN JD; PRINCE MA; KAMIJO T; OGAWA M; PHILLIPS JA
      DETECTION OF GROWTH-HORMONE GENE DEFECTS BY DIDEOXY FINGERPRINTING (DDF)

      Endocrine journal
    8. WAGNER JK; EBLE A; COGAN JD; PRINCE MA; PHILLIPS JA; MULLIS PE
      ALLELIC VARIATIONS IN THE HUMAN GROWTH HORMONE-1 GENE PROMOTER OF GROWTH HORMONE-DEFICIENT PATIENTS AND NORMAL CONTROLS

      European journal of endocrinology
    9. RASKIN S; COGAN JD; SUMMAR ML; MORENO A; KRISHNAMANI MRS; PHILLIPS JA
      GENETIC-MAPPING OF THE HUMAN PITUITARY-SPECIFIC TRANSCRIPTIONAL FACTOR GENE AND ITS ANALYSIS IN FAMILIAL PANHYPOPITUITARY DWARFISM

      Human genetics
    10. HAMID R; COGAN JD; JONES SN; TIBBETTS C
      PHENOTYPIC DETERMINANTS OF ADENOVIRUS E1A GENE AUTOREGULATION - VARIABLE REGION BETWEEN CONSERVED CODING DOMAIN-2 AND DOMAIN-3

      Virology
    11. COGAN JD; RAMEL B; LEHTO M; PHILLIPS J; PRINCE M; BLIZZARD RM; DERAVEL TJL; BRAMMERT M; GROOP L
      A RECURRING DOMINANT-NEGATIVE MUTATION CAUSES AUTOSOMAL-DOMINANT GROWTH-HORMONE DEFICIENCY - A CLINICAL RESEARCH-CENTER STUDY

      The Journal of clinical endocrinology and metabolism
    12. COGAN JD; PHILLIPS JA; SCHENKMAN SS; MILNER RDG; SAKATI N
      FAMILIAL GROWTH-HORMONE DEFICIENCY - A MODEL OF DOMINANT AND RECESSIVE MUTATIONS AFFECTING A MONOMERIC PROTEIN

      The Journal of clinical endocrinology and metabolism
    13. PHILLIPS JA; COGAN JD
      GENETIC-BASIS OF ENDOCRINE DISEASE-6 - MOLECULAR-BASIS OF FAMILIAL HUMAN GROWTH-HORMONE DEFICIENCY

      The Journal of clinical endocrinology and metabolism
    14. COGAN JD; PHILLIPS JA; SAKATI N; FRISCH H; SCHOBER E; MILNER RDG
      HETEROGENEOUS GROWTH-HORMONE (GH) GENE-MUTATIONS IN FAMILIAL GH DEFICIENCY

      The Journal of clinical endocrinology and metabolism
    15. PHILLIPS JA; COGAN JD; MILLENDAVIS S; MILNER RDG; SAKATI NA; SCHENKMAN SS; BUNDEY SE
      MOLECULAR-BASIS OF AUTOSOMAL RECESSIVE AND AUTOSOMAL-DOMINANT INHERITANCE OF FAMILIAL GH DEFICIENCY

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/21 alle ore 00:21:00