Catalogo Articoli (Spogli Riviste)

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La ricerca find articoli where soggetti phrase all words 'LARGE FAMILY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 43 riferimenti
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    1. Angres, B; Kim, L; Jung, R; Gessner, R; Tauber, R
      LI-cadherin gene expression during mouse intestinal development

      DEVELOPMENTAL DYNAMICS
    2. Takei, Y; Hamada, S; Senzaki, K; Mutoh, T; Sugino, H; Yagi, T
      Two novel CNRs from the CNR gene cluster have molecular features distinct from those of CNR1 to 8

      GENOMICS
    3. Ishihara, H; Kanda, F; Nishio, H; Sumino, K; Chihara, K
      Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy

      JOURNAL OF NEUROLOGY
    4. Cammarata, M; Vazzana, M; Chinnici, C; Parrinello, N
      A serum fucolectin isolated and characterized from sea bass Dicentrarchus labrax

      BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
    5. Nakajima, D; Nakayama, M; Kikuno, R; Hirosawa, M; Nagase, T; Ohara, O
      Identification of three novel non-classical cadherin genes through comprehensive analysis of large cDNAs

      MOLECULAR BRAIN RESEARCH
    6. Bertola, DR; Kim, CA; Pereira, AC; Mota, GFA; Krieger, JE; Vieira, IC; Valente, M; Loreto, MR; Magalhaes, RP; Gonzalez, CH
      Are Noonan syndrome and Noonan-like/multiple giant cell lesion syndrome distinct entities?

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Hilschmann, N; Barnikol, HU; Barnikol-Watanabe, S; Gotz, H; Kratzin, H; Thinnes, FP
      The immunoglobulin-like genetic predetermination of the brain: the protocadherins, blueprint of the neuronal network

      NATURWISSENSCHAFTEN
    8. Nakagawa, M; Matsuzaki, T; Suehara, M; Kanzato, N; Takashima, H; Higuchi, I; Matsumura, T; Goto, K; Arahata, K; Osame, M
      Phenotypic variation in a large Japanese family with Miyoshi myopathy withnonsense mutation in exon 19 of dysferlin gene

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    9. Hill, E; Broadbent, ID; Chothia, C; Pettitt, J
      Cadherin superfamily proteins in Caenorhabditis elegans and Drosophila melanogaster

      JOURNAL OF MOLECULAR BIOLOGY
    10. Homayouni, R; Rice, DS; Curran, T
      Disabled-1 interacts with a novel developmentally regulated protocadherin

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    11. Maciel, P; Costa, MDC; Ferro, A; Rousseau, M; Santos, CS; Gaspar, C; Barros, J; Rouleau, GA; Coutinho, P; Sequeiros, J
      Improvement in the molecular diagnosis of Machado-Joseph disease

      ARCHIVES OF NEUROLOGY
    12. Bruses, JL
      Cadherin-mediated adhesion at the interneuronal synapse

      CURRENT OPINION IN CELL BIOLOGY
    13. Blanco, P; Sargent, CA; Boucher, CA; Mitchell, M; Affara, NA
      Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain

      MAMMALIAN GENOME
    14. Yagi, T; Takeichi, M
      Cadherin superfamily genes: functions, genomic organization, and neurologic diversity

      GENES & DEVELOPMENT
    15. Sharp, A; Robinson, D; Jacobs, P
      Age- and tissue-specific variation of X chromosome inactivation ratios in normal women

      HUMAN GENETICS
    16. Rauen, KA; Cotter, PD; Bitts, SR; Cox, VA; Golabi, M
      Cardio-facio-cutaneous syndrome phenotype in an individual with an interstitial deletion of 12q: Identification of a candidate region for CFC syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. Bonnemann, CG; Cox, GF; Shapiro, F; Wu, JJ; Feener, CA; Thompson, TG; Anthony, DC; Eyre, DR; Darras, BT; Kunkel, LM
      A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    18. Suzuki, ST
      Recent progress in protocadherin research

      EXPERIMENTAL CELL RESEARCH
    19. Costa, JM; Vidaud, D; Laurendeau, I; Vidaud, M; Fressinaud, E; Moisan, JP; David, A; Meyer, D; Lavergne, JM
      Somatic mosaicism and compound heterozygosity in female hemophilia B

      BLOOD
    20. Tanner, SM; Orstavik, KH; Kristiansen, M; Lev, D; Lerman-Sagie, T; Sadeh, M; Liechti-Gallati, S
      Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother

      HUMAN GENETICS
    21. de Seze, J; Udd, B; Vermersch, P
      Tibial muscular dystrophy.

      REVUE NEUROLOGIQUE
    22. Van den Berg, H; Hennekam, RCM
      Acute lymphoblastic leukaemia in a patient with cardiofaciocutaneous syndrome

      JOURNAL OF MEDICAL GENETICS
    23. de Parseval, N; Alkabbani, H; Heidmann, T
      The long terminal repeats of the HERV-H human endogenous retrovirus contain binding sites for transcriptional regulation by the Myb protein

      JOURNAL OF GENERAL VIROLOGY
    24. Paassilta, P; Lohiniva, J; Annunen, S; Bonaventure, J; Le Merrer, M; Pai, L; Ala-Kokko, L
      COL9A3: A third locus for multiple epiphyseal dysplasia

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. Plenge, RM; Tranebjaerg, L; Jensen, PKA; Schwartz, C; Willard, HF
      Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation

      AMERICAN JOURNAL OF HUMAN GENETICS
    26. GURTUG O; HALILSOY M
      NEW COLLIDING WAVE SOLUTIONS IN THE EINSTEIN-ABELIAN GAUGE AND EINSTEIN-MAXWELL-DILATON THEORIES

      Nuovo cimento della Societa italiana di fisica. B, Relativity, classical a
    27. Naumova, AK; Olien, L; Bird, LM; Smith, M; Verner, AE; Leppert, M; Morgan, K; Sapienza, C
      Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

      EUROPEAN JOURNAL OF HUMAN GENETICS
    28. UDD B; HARAVUORI H; KALIMO H; PARTANEN J; PULKKINEN L; PAETAU A; PELTONEN L; SOMER H
      TIBIAL MUSCULAR-DYSTROPHY - FROM CLINICAL DESCRIPTION TO LINKAGE ON CHROMOSOME 2Q31

      Neuromuscular disorders
    29. KOOI AVD; GINJAAR HB; BUSCH HFM; WOKKE JHJ; BARTH PG; DEVISSER M
      LIMB-GIRDLE MUSCULAR-DYSTROPHY - A PATHOLOGICAL AND IMMUNOHISTOCHEMICAL REEVALUATION

      Muscle & nerve
    30. BIROUK N; LEGUERN E; MAISONOBE T; ROUGER H; GOUIDER R; TARDIEU S; GUGENHEIM M; ROUTON MC; LEGER JM; AGID Y; BRICE A; BOUCHE P
      X-LINKED CHARCOT-MARIE-TOOTH-DISEASE WITH CONNEXIN-32 MUTATIONS - CLINICAL AND ELECTROPHYSIOLOGIC STUDY

      Neurology
    31. ORSTAVIK KH; ORSTAVIK RE; NAUMOVA AK; DADAMO P; GEDEON A; BOLHUIS PA; BARTH PG; TONIOLO D
      X-CHROMOSOME INACTIVATION IN CARRIERS OF BARTH-SYNDROME

      American journal of human genetics
    32. YAGISHITA S; INOUE M
      CLINICOPATHOLOGY OF SPINOCEREBELLAR DEGENERATION - ITS CORRELATION TOTHE UNSTABLE CAG REPEAT OF THE AFFECTED GENE

      Pathology international
    33. KALTNER H; LIPS KS; REUTER G; LIPPERT S; SINOWATZ F; GABIUS HJ
      QUANTITATION AND HISTOCHEMICAL-LOCALIZATION OF GALECTIN-1 AND GALECTIN-1-REACTIVE GLYCOCONJUGATES IN FETAL DEVELOPMENT OF BOVINE ORGANS

      Histology and histopathology
    34. BOOTH A; CHURCHILL A; ANWAR R; MENAGE M; MARKHAM A
      THE GENETICS OF PRIMARY OPEN-ANGLE GLAUCOMA

      British journal of ophthalmology
    35. MOREIRA ES; VAINZOF M; MARIE SK; SERTIE AL; ZATZ M; PASSOSBUENO MR
      THE 7TH FORM OF AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHY ISMAPPED TO 17Q11-12

      American journal of human genetics
    36. FRANKE P; BARBE B; LEBOYER M; MAIER W
      FRAGILE-X SYNDROME .2. COGNITIVE AND BEHAVIORAL-CORRELATES OF MUTATIONS OF THE FMR-1 GENE

      European psychiatry
    37. MATSUMURA R; TAKAYANAGI T; FUJIMOTO Y; MURATA K; MANO Y; HORIKAWA H; CHUMA T
      THE RELATIONSHIP BETWEEN TRINUCLEOTIDE REPEAT LENGTH AND PHENOTYPIC VARIATION IN MACHADO-JOSEPH DISEASE

      Journal of the neurological sciences
    38. ADAR R; SHARON N
      MUTATIONAL STUDIES OF THE AMINO-ACID-RESIDUES IN THE COMBINING SITE OF ERYTHRINA CORALLODENDRON LECTIN

      European journal of biochemistry
    39. NOKELAINEN P; UDD B; SOMER H; PELTONEN L
      LINKAGE ANALYSES IN TIBIAL MUSCULAR-DYSTROPHY

      Human heredity
    40. GURTUG O
      A NEW EXTENSION OF THE FERRARI-IBANEZ COLLIDING WAVE SOLUTION

      General relativity and gravitation
    41. VANDERKOOI AJ; DEVISSER M; BARTH PG
      LIMB-GIRDLE MUSCULAR-DYSTROPHY - REAPPRAISAL OF A REJECTED ENTITY

      Clinical neurology and neurosurgery
    42. PARTANEN J; LAULUMAA V; PALJARVI L; PARTANEN K; NAUKKARINEN A
      LATE-ONSET FOOT-DROP MUSCULAR-DYSTROPHY WITH RIMMED VACUOLES

      Journal of the neurological sciences
    43. RAVEAU B; BOREL MM; LECLAIRE A; GRANDIN A
      NIOBIUM PHOSPHATE BRONZES - STRUCTURAL RELATIONSHIPS WITH PURE OCTAHEDRAL OXYGEN TUNGSTEN BRONZES

      International journal of modern physics b


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/10/20 alle ore 05:19:55