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La ricerca find articoli where soggetti phrase all words 'FIBRILLIN 1' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 88 riferimenti
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    1. Robinson, PN; Booms, P
      The molecular pathogenesis of the Marfan syndrome

      CELLULAR AND MOLECULAR LIFE SCIENCES
    2. Marque, V; Kieffer, P; Gayraud, B; Lartaud-Idjouadiene, I; Ramirez, F; Atkinson, J
      Aortic wall mechanics and composition in a transgenic mouse model of Marfan syndrome

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    3. Tiecke, F; Katzke, S; Booms, P; Robinson, PN; Neumann, L; Godfrey, M; Mathews, KR; Scheuner, M; Hinkel, GK; Brenner, RE; Hovels-Gurich, HH; Hagemeier, C; Fuchs, J; Skovby, F; Rosenberg, T
      Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Morrissette, JJD; Colliton, RP; Spinner, NB
      Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndrome

      HUMAN MOLECULAR GENETICS
    5. Eldadah, ZA; Hamosh, A; Biery, NJ; Montgomery, RA; Duke, M; Elkins, R; Dietz, HC
      Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

      HUMAN MOLECULAR GENETICS
    6. Gigante, A; Chillemi, C; Quaglino, D; Miselli, M; Pasquali-Ronchetti, I
      DL-penicillamine induced alteration of elastic fibers of periosteum-perichondrium and associated growth inhibition: an experimental study

      JOURNAL OF ORTHOPAEDIC RESEARCH
    7. Lo, IFM; Wong, RMS; Lam, FWF; Tong, TMF; Lam, STS
      Missense mutations of the fibrillin-1 gene in two Chinese patients with severe Marfan syndrome

      CHINESE MEDICAL JOURNAL
    8. Hutchinson, S; Wordsworth, BP; Handford, PA
      Marfan syndrome caused by a mutation in FBN1 that gives rise to cryptic splicing and a 33 nucleotide insertion in the coding sequence

      HUMAN GENETICS
    9. Oble, DA; Teh, HS
      Tight skin mouse subcutaneous hypertrophy can occur in the absence of up Tcell receptor-bearing lymphocytes

      JOURNAL OF RHEUMATOLOGY
    10. Simkin, PA
      Acetabular osteitis in ankylosing spondylitis: Does fibrillin figure in its pathogenesis?

      JOURNAL OF RHEUMATOLOGY
    11. Sterzel, RB; Hartner, A; Hilgers, KF; Bressan, GM
      Contribution of the mesangium to elastic strength and anchorage of the glomerular capillary tuft

      ADVANCED GLYCATION END PRODUCTS IN NEPHROLOGY
    12. Akhtar, S; Bron, AJ; Meek, KM; Bennett, K
      Congenital hereditary endothelial dystrophy and band keratopathy in an infant with corpus callosum agenesis

      CORNEA
    13. Pandey, JP; Page, GP; Silver, RM; LeRoy, EC; Bona, CA
      Anti-fibrillin-1 autoantibodies in systemic sclerosis are GM and KM allotype-restricted

      EXPERIMENTAL AND CLINICAL IMMUNOGENETICS
    14. Toudjarska, I; Kilpatrick, MW; Lembessis, P; Carra, S; Harton, GL; Sisson, ME; Black, SH; Stern, HJ; Gelman-Kohan, Z; Shohat, M; Tsipouras, P
      Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis

      AMERICAN JOURNAL OF MEDICAL GENETICS
    15. Judge, DP; Biery, NJ; Dietz, HC
      Characterization of microsatellite markers flanking FBN1: Utility in the diagnostic evaluation for Marfan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    16. Guo, D; Tan, FK; Cantu, A; Plon, SE; Milewicz, DM
      FBN1 exon 2 splicing error in a patient with Marfan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    17. McGaha, T; Saito, S; Phelps, RG; Gordon, R; Noben-Trauth, N; Paul, WE; Bona, C
      Lack of skin fibrosis in tight skin (TSK) mice with targeted mutation in the interleukin-4R alpha and transforming growth factor-beta genes

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    18. Unsold, C; Hyytiainen, M; Bruckner-Tuderman, L; Keski-Oja, J
      Latent TGF-beta binding protein LTBP-1 contains three potential extracellular matrix interacting domains

      JOURNAL OF CELL SCIENCE
    19. Pepe, G; Giusti, B; Evangelisti, L; Porciani, MC; Brunelli, T; Giurlani, L; Attanasio, M; Fattori, R; Bagni, C; Comeglio, P; Abbate, R; Gensini, GF
      Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: genotype-phenotype correlation

      CLINICAL GENETICS
    20. Bunton, TE; Biery, NJ; Myers, L; Gayraud, B; Ramirez, F; Dietz, HC
      Phenotypic alteration of vascular smooth muscle cells precedes elastolysisin a mouse model of Marfan syndrome

      CIRCULATION RESEARCH
    21. Hunzelmann, N; Nischt, R; Brenneisen, P; Eickert, A; Krieg, T
      Increased deposition of fibulin-2 in solar elastosis and its colocalization with elastic fibres

      BRITISH JOURNAL OF DERMATOLOGY
    22. Malby, S; Pickering, R; Saha, S; Smallridge, R; Linse, S; Downing, AK
      The first epidermal growth factor-like domain of the low-density lipoprotein receptor contains a noncanonical calcium binding site

      BIOCHEMISTRY
    23. Osakabe, T; Hayashi, M; Hasegawa, K; Okuaki, T; Ritty, TM; Mecham, RP; Wachi, H; Seyama, Y
      Age- and gender-related changes in ligament components

      ANNALS OF CLINICAL BIOCHEMISTRY
    24. Denton, CP; Bing, Z; Xu, SW; Zhang, ZP; Bou-Gharios, G; Eberspaecher, H; Black, CM; de Crombrugghe, B
      Activation of a fibroblast-specific enhancer of the Pro alpha 2(I) collagen gene in tight-skin mice

      ARTHRITIS AND RHEUMATISM
    25. Dodig, TD; Mack, KT; Cassarino, DF; Clark, SH
      Development of the tight-skin phenotype in immune-deficient mice

      ARTHRITIS AND RHEUMATISM
    26. Chikumi, H; Yamamoto, T; Ohta, Y; Nanba, E; Nagata, K; Ninomiya, H; Narasaki, K; Katoh, T; Hisatome, I; Ono, K; Tanaka, Y; Kuroda, H; Ohgi, S
      Fibrillin gene (FBN1) mutations in Japanese patients with Marfan syndrome

      JOURNAL OF HUMAN GENETICS
    27. Kettle, S; Cardy, CM; Hutchinson, S; Sykes, B; Handford, PA
      Characterisation of fibrillin-1 cDNA clones in a human fibroblast cell line that assembles microfibrils

      INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
    28. Saharinen, J; Keski-Oja, J
      Specific sequence motif of 8-Cys repeats of TGF-beta binding proteins, LTBPs, creates a hydrophobic interaction surface for binding of small latent TGF-beta

      MOLECULAR BIOLOGY OF THE CELL
    29. McGettrick, AJ; Knott, V; Willis, A; Handford, PA
      Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context

      HUMAN MOLECULAR GENETICS
    30. Milewicz, DM; Urban, Z; Boyd, C
      Genetic disorders of the elastic fiber system

      MATRIX BIOLOGY
    31. Dietz, HC; Mecham, RP
      Mouse models of genetic diseases resulting from mutations in elastic fiberproteins

      MATRIX BIOLOGY
    32. Lundberg, I; Antohi, S; Takeuki, K; Arnett, F; Steiner, G; Brumeanu, TD; Klareskog, L; Bona, C
      Kinetics of anti-fibrillin-1 autoantibodies in MCTD and CREST syndrome

      JOURNAL OF AUTOIMMUNITY
    33. Katsanis, N; Venable, S; Smith, JR; Lupski, JR
      Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13

      HUMAN GENETICS
    34. Burke, RD; Wang, D; Mark, S; Martens, G
      Distribution of fibrillin 1 in extracellular matrix and epithelia during early development of avian embryos

      ANATOMY AND EMBRYOLOGY
    35. Dawson, PA; Marini, JC
      Hammerhead ribozymes selectively suppress mutant type I collagen mRNA in osteogenesis imperfecta fibroblasts

      NUCLEIC ACIDS RESEARCH
    36. Laudahn, BM; Gyurus, P; Orth, U; Gal, A; Nienaber, CA
      Indirect genotype analysis as a tool for diagnosis of Marfan syndrome

      ZEITSCHRIFT FUR KARDIOLOGIE
    37. Handford, PA
      Fibrillin-1, a calcium binding protein of extracellular matrix

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
    38. Pyeritz, RE
      The Marfan syndrome

      ANNUAL REVIEW OF MEDICINE
    39. Krumdieck, CL; Prince, CW
      Mechanisms of homocysteine toxicity on connective tissues: Implications for the morbidity of aging

      JOURNAL OF NUTRITION
    40. Werner, JM; Knott, V; Handford, PA; Campbell, ID; Downing, AK
      Backbone dynamics of a cbEGF domain pair in the presence of calcium

      JOURNAL OF MOLECULAR BIOLOGY
    41. Maddox, BK; Mokashi, A; Keene, DR; Bachinger, HP
      A cartilage oligomeric matrix protein mutation associated with pseudoachondroplasia changes the structural and functional properties of the type 3 domain

      JOURNAL OF BIOLOGICAL CHEMISTRY
    42. Megarbane, A; Mustapha, M; Bleik, J; Waked, N; Delague, V; Loiselet, J
      Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family

      CLINICAL GENETICS
    43. Muranyi, A; Evenas, J; Stenberg, Y; Stenflo, J; Drakenberg, T
      Characterization of the EGF-like module pair 3-4 from vitamin K-dependent protein S using NMR spectroscopy reveals dynamics on three separate time scales and extensive effects from calcium binding

      BIOCHEMISTRY
    44. Hata, RI; Akai, J; Kimura, A; Ishikawa, O; Kuwana, M; Shinkai, H
      Association of functional microsatellites in the human type I collagen alpha 2 chain (COL1A2) gene with systemic sclerosis

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    45. Zhou, XD; Tan, FK; Stivers, DN; Arnett, FC
      Microsatellites and intragenic polymorphisms of transforming growth factorbeta and platelet-derived growth factor and their receptor genes in NativeAmericans with systemic sclerosis (scleroderma) - A preliminary analysis showing no genetic association

      ARTHRITIS AND RHEUMATISM
    46. Vella, F; Hernandez, JF; Molla, A; Block, MR; Arlaud, GJ
      Grafting an RGD motif onto an epidermal growth factor-like module: chemical synthesis and functional characterization of the chimeric molecule

      JOURNAL OF PEPTIDE RESEARCH
    47. Suwabe, H; Serizawa, A; Kajiwara, H; Ohkido, M; Tsutsumi, Y
      Degenerative processes of elastic fibers in sun-protected and sun-exposed skin: Immunoelectron microscopic observation of elastin, fibrillin-1, amyloid P component, lysozyme and alpha(1)-antitrypsin

      PATHOLOGY INTERNATIONAL
    48. Yuan, B; Thomas, JP; von Kodolitsch, Y; Pyeritz, RE
      Comparison of heteroduplex analysis, direct sequencing, and enzyme mismatch cleavage for detecting mutations in a large gene, FBN1

      HUMAN MUTATION
    49. Adachi, M; Tachibana, K; Asakura, Y; Suwa, S; Nishimura, G
      A male patient presenting with major clinical symptoms of glucocorticoid deficiency and skeletal dysplasia, showing a steroid pattern compatible with17 alpha-hydroxylase/17,20-lyase deficiency, but without obvious CYP17 gene mutations

      ENDOCRINE JOURNAL
    50. Halliday, D; Hutchinson, S; Kettle, S; Firth, H; Wordsworth, P; Handford, PA
      Molecular analysis of eight mutations in FBN1

      HUMAN GENETICS
    51. Weidenbach, M; Brenner, R; Rantamaki, T; Redel, DA
      Acute mitral regurgitation due to chordal rupture in a patient with neonatal Marfan syndrome caused by a deletion in exon 29 of the FBN1 gene

      PEDIATRIC CARDIOLOGY
    52. Fattori, R; Nienaber, CA; Descovich, B; Ambrosetto, P; Reggiani, LB; Pepe, G; Kaufmann, U; Negrini, N; von Kodolitsch, Y; Gensini, GF
      Importance of dural ectasia in phenotypic assessment of Marfan's syndrome

      LANCET
    53. Stenberg, Y; Muranyi, A; Steen, C; Thulin, E; Drakenberg, T; Stenflo, J
      EGF-like module pair 3-4 in vitamin K-dependent protein S: Modulation of calcium affinity of module 4 by module 3, and interaction with factor X

      JOURNAL OF MOLECULAR BIOLOGY
    54. Raghunath, M; Putnam, EA; Ritty, T; Hamstra, D; Park, ES; Tschodrich-Rotter, M; Peters, R; Rehemtulla, A; Milewicz, DM
      Carboxy-terminal conversion of profibrillin to fibrillin at a basic site by PACE/furin-like activity required for incorporation in the matrix

      JOURNAL OF CELL SCIENCE
    55. Estienne, V; Blanchet, C; Niccoli-Sire, P; Duthoit, C; Durand-Gorde, JM; Geourjon, C; Baty, D; Carayon, P; Ruf, J
      Molecular model, calcium sensitivity, and disease specificity of a conformational thyroperoxidase B-cell epitope

      JOURNAL OF BIOLOGICAL CHEMISTRY
    56. Booms, P; Cisler, J; Mathews, KR; Godfrey, M; Tiecke, F; Kaufmann, UC; Vetter, U; Hagemeier, C; Robinson, PN
      Novel exon skipping mutation in the fibrillin-1 gene: Two 'hot spots' for the neonatal Marfan syndrome

      CLINICAL GENETICS
    57. McGrory, J; Cole, WG
      Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndrome

      CLINICAL GENETICS
    58. Ong, CJ; Ip, S; Teh, SJ; Wong, C; Jirik, FR; Grusby, MJ; Teh, HS
      A role for T helper 2 cells in mediating skin fibrosis in tight-skin mice

      CELLULAR IMMUNOLOGY
    59. Kilpatrick, MW; Lembessis, P; Rose, E; Tsipouras, P
      A novel G to a substitution at nucleotide 1734 of the FBN1 gene predictinga C534Y mutation responsible for Marfan syndrome

      HUMAN HEREDITY
    60. Sinha, S; Nevett, C; Shuttleworth, CA; Kielty, CM
      Cellular and extracellular biology of the latent transforming growth factor-beta binding proteins

      MATRIX BIOLOGY
    61. MURAI C; SAITO S; KASTURI KN; BONA CA
      SPONTANEOUS OCCURRENCE OF ANTI-FIBRILLIN-1 AUTOANTIBODIES IN TIGHT-SKIN MICE

      Autoimmunity (Print)
    62. BABCOCK D; GASNER C; FRANCKE U; MASLEN C
      A SINGLE MUTATION THAT RESULTS IN AN ASP TO HIS SUBSTITUTION AND PARTIAL EXON SKIPPING IN A FAMILY WITH CONGENITAL CONTRACTURAL ARACHNODACTYLY

      Human genetics
    63. KOO HP; MACARAK EJ; CHANG SL; ROSENBLOOM J; HOWARD PS
      TEMPORAL EXPRESSION OF ELASTIC FIBER COMPONENTS IN BLADDER DEVELOPMENT

      Connective tissue research
    64. VONKODOLITSCH Y; RAGHUNATH M; NIENABER CA
      THE MARFAN-SYNDROME - PREVALENCE AND NATU RAL-HISTORY OF CARDIOVASCULAR MANIFESTATIONS

      Zeitschrift fur Kardiologie
    65. VONKODOLITSCH Y; RAGHUNATH M; DIECKMANN C; NIENABER CA
      THE MARFAN-SYNDROME - DIAGNOSIS OF THE CA RDIOVASCULAR MANIFESTATIONS

      Zeitschrift fur Kardiologie
    66. LJUBIMOV AV; SAGHIZADEH M; SPIRIN KS; MECHAM RP; SAKAI LY; KENNEY MC
      INCREASED EXPRESSION OF FIBRILLIN-1 IN HUMAN CORNEAS WITH BULLOUS KERATOPATHY

      Cornea
    67. GREALLY MT; CAREY JC; MILEWICZ DM; HUDGINS L; GOLDBERG RB; SHPRINTZEN RJ; COUSINEAU AJ; SMITH WL; JUDISCH GF; HANSON JW
      SHPRINTZEN-GOLDBERG-SYNDROME - A CLINICAL ANALYSIS

      American journal of medical genetics
    68. CARDY CM; HANDFORD PA
      METAL-ION DEPENDENCY OF MICROFIBRILS SUPPORTS A ROD-LIKE CONFORMATIONFOR FIBRILLIN-1 CALCIUM-BINDING EPIDERMAL GROWTH FACTOR-LIKE DOMAINS

      Journal of Molecular Biology
    69. DIRLAMSCHATZ KA; ATTIE AD
      CALCIUM INDUCES A CONFORMATIONAL CHANGE IN THE LIGAND-BINDING DOMAIN OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR

      Journal of lipid research
    70. Prahlow, JA; Barnard, JJ; Milewicz, DM
      Familial thoracic aortic aneurysms and dissections

      JOURNAL OF FORENSIC SCIENCES
    71. OKLU R; METCALFE JC; HESKETH TR; KEMP PR
      LOSS OF A CONSENSUS HEPARIN-BINDING SITE BY ALTERNATIVE SPLICING OF LATENT TRANSFORMING-GROWTH-FACTOR-BETA BINDING PROTEIN-1

      FEBS letters
    72. LJUBIMOV AV; ALBA SA; BURGESON RE; NINOMIYA Y; SADO Y; SUN TT; NESBURN AB; KENNEY MC; MAGUEN E
      EXTRACELLULAR-MATRIX CHANGES IN HUMAN CORNEAS AFTER RADIAL KERATOTOMY

      Experimental Eye Research
    73. GIBSON MA; ELLIS SL; ADES LC; HAAN E; CLEARY EG
      PREFERENTIAL PRE-MESSENGER-RNA UTILIZATION OF AN UPSTREAM CRYPTIC 5'-SPLICE-SITE CREATED BY A SINGLE-BASE DELETION MUTATION IN EXON-37 OF THE FBN-1 GENE

      European journal of biochemistry
    74. MILEWICZ DM; CHEN H; PARK ES; PETTY EM; ZAGHI H; PAI S; WILLING M; PATEL V
      REDUCED PENETRANCE AND VARIABLE EXPRESSIVITY OF FAMILIAL THORACIC AORTIC ANEURYSMS DISSECTIONS/

      The American journal of cardiology
    75. RAND MD; LINDBLOM A; CARLSON J; VILLOUTREIX BO; STENFLO J
      CALCIUM-BINDING TO TANDEM REPEATS OF EGF-LIKE MODULES - EXPRESSION AND CHARACTERIZATION OF THE EGF-LIKE MODULES OF HUMAN NOTCH-1 IMPLICATEDIN RECEPTOR-LIGAND INTERACTIONS

      Protein science
    76. KASTURI KN; HATAKEYAMA A; MURAI C; GORDON R; PHELPS RG; BONA CA
      B-CELL DEFICIENCY DOES NOT ABROGATE DEVELOPMENT OF CUTANEOUS HYPERPLASIA IN MICE INHERITING THE DEFECTIVE FIBRILLIN-1 GENE

      Journal of autoimmunity
    77. YUAN XM; DOWNING AK; KNOTT V; HANDFORD PA
      SOLUTION STRUCTURE OF THE TRANSFORMING-GROWTH-FACTOR BETA-BINDING PROTEIN-LIKE MODULE, A DOMAIN ASSOCIATED WITH MATRIX FIBRILS

      EMBO journal
    78. ADAM S; GOHRING W; WIEDEMANN H; CHU ML; TIMPL R; KOSTKA G
      BINDING OF FIBULIN-1 TO NIDOGEN DEPENDS ON ITS C-TERMINAL GLOBULAR DOMAIN AND A SPECIFIC ARRAY OF CALCIUM-BINDING EPIDERMAL GROWTH FACTOR-LIKE (EG) MODULES

      Journal of Molecular Biology
    79. PEPE G; GIUSTI B; ATTANASIO M; COMEGLIO P; PORCIANI MC; GIURLANI L; MONTESI GF; CALAMAI GC; VACCARI M; FAVILLI S; ABBATE R; GENSINI GF
      A MAJOR INVOLVEMENT OF THE CARDIOVASCULAR-SYSTEM IN PATIENTS AFFECTEDBY MARFAN-SYNDROME - NOVEL MUTATIONS IN FIBRILLIN-1 GENE

      Journal of Molecular and Cellular Cardiology
    80. WERTH VP; WILLIAMS KJ; FISHER EA; BASHIR M; ROSENBLOOM J; SHI XM
      UVB IRRADIATION ALTERS CELLULAR-RESPONSES TO CYTOKINES - ROLE IN EXTRACELLULAR-MATRIX GENE-EXPRESSION

      Journal of investigative dermatology
    81. GIBSON MA; KUMARATILAKE JS; CLEARY EG
      IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL-LOCALIZATION OF MP78 70 (BETA-IG-H3) IN EXTRACELLULAR-MATRIX OF DEVELOPING AND MATURE BOVINE-TISSUES/

      The Journal of histochemistry and cytochemistry
    82. STENBERG Y; LINSE S; DRAKENBERG T; STENFLO J
      THE HIGH-AFFINITY CALCIUM-BINDING SITES IN THE EPIDERMAL GROWTH-FACTOR MODULE REGION OF VITAMIN-K-DEPENDENT PROTEIN-S

      The Journal of biological chemistry
    83. KILPATRICK MW; HARTON GL; PHYLACTOU LA; LEVINSON G; FUGGER EF; SCHULMAN JD; BLACK SH; TSIPOURAS P
      PREIMPLANTATION GENETIC DIAGNOSIS IN MARFAN-SYNDROME

      Fetal diagnosis and therapy
    84. WIRTZ MK; SAMPLES JR; KRAMER PL; RUST K; YOUNT J; ACOTT TS; KOLER RD; CISLER J; JAHED A; GORLIN RJ; GODFREY M
      WEILL-MARCHESANI SYNDROME - POSSIBLE LINKAGE OF THE AUTOSOMAL-DOMINANT FORM TO 15Q21.1

      American journal of medical genetics
    85. PUTNAM EA; CHO M; ZINN AB; TOWBIN JA; BYERS PH; MILEWICZ DM
      DELINEATION OF THE MARFAN PHENOTYPE ASSOCIATED WITH MUTATIONS IN EXONS 23-32 OF THE FBN1 GENE

      American journal of medical genetics
    86. ADES LC; HAAN EA; COLLEY AF; RICHARDS RI
      CHARACTERIZATION OF 4 NOVEL FIBRILLIN-1 (FBN1) MUTATIONS IN MARFAN-SYNDROME

      Journal of Medical Genetics
    87. PFAFF M; REINHARDT DP; SAKAI LY; TIMPL R
      CELL-ADHESION AND INTEGRIN BINDING TO RECOMBINANT HUMAN FIBRILLIN-1

      FEBS letters
    88. JACOBSON SL; KIMBERLY D; THORNBURG K; MASLEN C
      LOCALIZATION OF FIBRILLIN-1 IN THE HUMAN TERM PLACENTA

      Journal of the Society for Gynecologic Investigation


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Documento generato il 05/06/20 alle ore 15:46:52