Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where authors phrase all words ' Nakae, J' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 37 riferimenti
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    1. Ishikawa, Y; Tajima, T; Nakae, J; Nagashima, T; Satoh, K; Okuhara, K; Fujieda, K
      Two mutations of the Gs alpha gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia

      JOURNAL OF HUMAN GENETICS
    2. Nakae, J; Kido, Y; Accili, D
      Tissue-specific insulin resistance in type 2 diabetes: lessons from gene-targeted mice

      ANNALS OF MEDICINE
    3. Nakae, J; Kitamura, T; Silver, DL; Accili, D
      The forkhead transcription factor Foxo1 (Fkhr) confers insulin sensitivityonto glucose-6-phosphatase expression

      JOURNAL OF CLINICAL INVESTIGATION
    4. Tajima, T; Fujieda, K; Kouda, N; Nakae, J; Miller, WL
      Heterozygous mutation in the cholesterol side chain cleavage enzyme (P450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    5. Kido, Y; Nakae, J; Accili, D
      Clinical review 125 - The insulin receptor and its cellular targets

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    6. Adachi, M; Tachibana, K; Asakura, Y; Abe, S; Nakae, J; Tajima, T; Fujieda, K
      Clinical case seminar - Compound heterozygous mutations in the gamma subunit gene of ENaC (1627delG and 1570-1G -> A) in one sporadic Japanese patient with a systemic form of pseudohypoaldosteronism type 1

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    7. Nakae, J; Kitamura, T; Ogawa, W; Kasuga, M; Accili, D
      Insulin regulation of gene expression through the forkhead transcription factor Foxo1 (Fkhr) requires kinases distinct from Akt

      BIOCHEMISTRY
    8. Okuhara, K; Tajima, T; Nakae, J; Fujieda, K
      A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversal

      JOURNAL OF HUMAN GENETICS
    9. Okuhara, K; Tajima, T; Abe, S; Satoh, K; Nakae, J; Shinohara, N; Fujieda, K
      Gonadotropin-releasing hormone analog therapy failed to improve predicted final height in two children with central precocious puberty and microcephalus

      ENDOCRINE JOURNAL
    10. Nakae, J; Barr, V; Accili, D
      Differential regulation of gene expression by insulin and IGF-1 receptors correlates with phosphorylation of a single amino acid residue in the forkhead transcription factor FKHR

      EMBO JOURNAL
    11. Sato, K; Tajima, T; Nakae, J; Adachi, M; Asakura, Y; Tachibana, K; Suwa, S; Katsumata, N; Tanaka, T; Hayashi, Y; Abe, S; Murashita, M; Okuhara, K; Shinohara, N; Fujieda, K
      Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets

      PEDIATRIC RESEARCH
    12. Tajima, T; Kitagawa, H; Yokoya, S; Tachibana, K; Adachi, M; Nakae, J; Suwa, S; Katoh, S; Fujieda, K
      A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    13. Tomizawa, M; Kumar, A; Perrot, V; Nakae, J; Accili, D; Rechler, MM
      Insulin inhibits the activation of transcription by a C-terminal fragment of the forkhead transcription factor FKHR: a mechanism for insulin inhibition of insulin-like growth factor binding protein-1 transcription (vol 275, pg 7289, 2000)

      JOURNAL OF BIOLOGICAL CHEMISTRY
    14. Tomizawa, M; Kumaro, A; Perrot, V; Nakae, J; Accili, D; Rechler, MM
      Insulin inhibits the activation of transcription by a C-terminal fragment of the forkhead transcription factor FKHR - A mechanism for insulin inhibition of insulin-like growth factor-binding protein-1 transcription

      JOURNAL OF BIOLOGICAL CHEMISTRY
    15. Nakae, J; Stoward, PJ; Shono, M; Matsuzaki, T
      Localisation and quantification of dehydrogenase activities in single muscle fibres of mdx gastrocnemius

      HISTOCHEMISTRY AND CELL BIOLOGY
    16. Okuhara, K; Tajima, T; Nakae, J; Sasaki, S; Tochimaru, H; Abe, S; Fujieda, K
      A Japanese case with Frasier syndrome caused by the splice junction mutation of WT1 gene

      ENDOCRINE JOURNAL
    17. Accili, D; Nakae, J; Kim, JJ; Park, BC; Rother, KI
      Targeted gene mutations define the roles of insulin and IGF-I receptors inmouse embryonic development

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    18. Nakae, J; Accili, D
      The mechanism of insulin action

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    19. Murashita, M; Tajima, T; Nakae, J; Shinohara, N; Geffner, ME; Fujieda, K
      Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-1 - A case report

      HORMONE RESEARCH
    20. Abe, S; Nakae, J; Yasoshima, K; Tajima, T; Shinohara, N; Murashita, M; Satoh, K; Koike, A; Takahashi, Y; Fujieda, K
      Novel missense mutation (Leu466Arg) of the DAX1 gene in a patient with X-linked congenital adrenal hypoplasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    21. Nakae, J; Park, BC; Accili, D
      Insulin stimulates phosphorylation of the forkhead transcription factor FKHR on serine 253 through wortmannin-sensitive pathway

      JOURNAL OF BIOLOGICAL CHEMISTRY
    22. TAJIMA T; FUJIEDA K; NAKAE J; MIKAMI A; CUTLER GB
      MUTATIONS OF THE CYP21 GENE IN NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY IN JAPAN

      Endocrine journal
    23. TAJIMA T; FUJIEDA K; MIKAMI A; IGARASHI Y; NAKAE J; CUTLER GB
      PRENATAL-DIAGNOSIS OF STEROID 21-HYDROXYLASE DEFICIENCY BY THE MODIFIED POLYMERASE-CHAIN-REACTION TO DETECT SPLICE-SITE MUTATION IN THE CYP21 GENE

      Endocrine journal
    24. NAKAE J; KATO M; MURASHITA M; SHINOHARA N; TAJIMA T; FUJIEDA K
      LONG-TERM EFFECT OF RECOMBINANT HUMAN INSULIN-LIKE-GROWTH-FACTOR-I ONMETABOLIC AND GROWTH-CONTROL IN A PATIENT WITH LEPRECHAUNISM

      The Journal of clinical endocrinology and metabolism
    25. NAKAE J; TAJIMA T; SUGAWARA T; ARAKANE F; HENAKI K; HOTSUBO T; IGARASHI N; IGARASHI Y; ISHII T; KODA N; KONDO T; KOHNO H; NAKAGAWA Y; TACHIBANA K; TAKESHIMA Y; TSUBOUCHI K; STRAUSS JF; FUJIEDA K
      ANALYSIS OF THE STEROIDOGENIC ACUTE REGULATORY PROTEIN (STAR) GENE INJAPANESE PATIENTS WITH CONGENITAL LIPOID ADRENAL-HYPERPLASIA

      Human molecular genetics
    26. TAJIMA T; MIKAMI A; FUKUSHI M; NAKAE J; KIKUCHI Y; FUJIEDA K
      CONVENTIONAL MOLECULAR DIAGNOSIS OF STEROID 21-HYDROXYLASE DEFICIENCYUSING MISMATCHED PRIMERS AND POLYMERASE CHAIN-REACTION

      Endocrine research
    27. TAJIMA T; NISHI Y; TAKASE A; NAKAE J; MURASHITA M; FUJIEDA K
      NO GENETIC MUTATION IN TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE IN PATIENTS WITH BIOCHEMICAL-EVIDENCE OF ENZYME DEFICIENCY

      Hormone research
    28. FUJIEDA K; TAJIMA T; NAKAE J; SAGESHIMA S; TACHIBANA K; SUWA S; SUGAWARA T; STRAUSS JF
      SPONTANEOUS PUBERTY IN 46,XX SUBJECTS WITH CONGENITAL LIPOID ADRENAL-HYPERPLASIA - OVARIAN STEROIDOGENESIS IS SPARED TO SOME EXTENT DESPITEINACTIVATING MUTATIONS IN THE STEROIDOGENIC ACUTE REGULATORY PROTEIN (STAR) GENE

      The Journal of clinical investigation
    29. TAJIMA T; FUJIEDA K; NAKAE J; TOYOURA T; SHIMOZAWA K; KUSUDA S; GOJI K; NAGASHIMA T; CUTLER GB
      MOLECULAR-BASIS OF NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY DETECTED BY NEONATAL MASS-SCREENING IN JAPAN

      The Journal of clinical endocrinology and metabolism
    30. NAKAE J; ABE S; TAJIMA T; SHINOHARA N; MURASHITA M; IGARASHI Y; KUSUDA S; SUZUKI J; FUJIEDA K
      3 NOVEL MUTATIONS AND A DE-NOVO DELETION MUTATION OF THE DAX-1 GENE IN PATIENTS WITH X-LINKED ADRENAL HYPOPLASIA CONGENITA

      The Journal of clinical endocrinology and metabolism
    31. TAJIMA T; NAKAE J; TAKEKOSHI Y; TAKAHASHI Y; YURI K; NAGASHIMA T; FUJIEDA K
      3 NOVEL AVPR2 MUTATIONS IN 3 JAPANESE FAMILIES WITH X-LINKED NEPHROGENIC DIABETES-INSIPIDUS

      Pediatric research
    32. NAKAE J; TAJIMA T; KUSUDA S; KOHDA N; OKABE T; SHINOHARA N; KATO M; MURASHITA M; MUKAI T; IMANAKA K; FUJIEDA K
      TRUNCATION AT THE C-TERMINUS OF THE DAX-1 PROTEIN IMPAIRS ITS BIOLOGICAL ACTIONS IN PATIENTS WITH X-LINKED ADRENAL HYPOPLASIA CONGENITA

      The Journal of clinical endocrinology and metabolism
    33. TAJIMA T; FUJIEDA K; NAKAE J; SHINOHARA N; YOSHIMOTO M; BABA T; KINOSHITA E; IGARASHI Y; OOMURA T
      MOLECULAR ANALYSIS OF TYPE-II 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE IN JAPANESE PATIENTS WITH CLASSICAL 3-BETA-HYDROXYSTEROID DEHYDROGENASE-DEFICIENCY

      Human molecular genetics
    34. TONOKI H; NAKAE J; TAJIMA T; SHINOHARA N; MONJI J; SATOH S; FUJIEDA K
      PREDOMINANCE OF THE MUTATION AT 1138 OF THE CDNA FOR THE FIBROBLAST-GROWTH-FACTOR-RECEPTOR-3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA

      Japanese journal of human genetics
    35. NAKAE J; MORIOKA H; OHTSUKA E; FUJIEDA K
      REPLACEMENTS OF LEUCINE-87 IN HUMAN INSULIN-RECEPTOR ALTER AFFINITY FOR INSULIN

      The Journal of biological chemistry
    36. TAJIMA T; NAKAE J; SHINOHARA N; FUJIEDA K
      A NOVEL MUTATION LOCALIZED IN THE 3' NON-HMG BOX REGION OF THE SRY GENE IN 46,XY GONADAL-DYSGENESIS

      Human molecular genetics
    37. MATSUMOTO M; NOMIYAMA T; NAKAE J; NISHIKAWA H
      COMBINATION CHEMOTHERAPY FOR A SENILE PATIENT WITH ADENOID CYSTIC CARCINOMA OF THE ESOPHAGUS - A CASE-REPORT

      Japanese Journal of Clinical Oncology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 08:54:25