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    1. Robinson, PN; Booms, P
      The molecular pathogenesis of the Marfan syndrome

      CELLULAR AND MOLECULAR LIFE SCIENCES
    2. Ritch, R; Schlotzer-Schrehardt, U
      Exfoliation (pseudoexfoliation) syndrome: toward a new understanding - Proceedings of the First International Think Tank

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    3. 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
    4. Boyer, AS; Runyan, RB
      TGF beta type III and TGF beta type II receptors have distinct activities during epithelial-mesenchymal cell transformation in the embryonic heart

      DEVELOPMENTAL DYNAMICS
    5. 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
    6. Sherratt, MJ; Wess, TJ; Baldock, C; Ashworth, JL; Purslow, PP; Shuttleworth, CA; Kielty, CM
      Fibrillin-rich microfibrils of the extracellular matrix: ultrastructure and assembly

      MICRON
    7. Morrissette, JJD; Colliton, RP; Spinner, NB
      Defective intracellular transport and processing of JAG1 missense mutations in Alagille syndrome

      HUMAN MOLECULAR GENETICS
    8. 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
    9. Hanssen, E; Franc, S; Garrone, R
      Synthesis and structural organization of zonular fibers during developmentand aging

      MATRIX BIOLOGY
    10. Farrell, AM; Dean, D; Millard, PR; Charnock, FM; Wojnarowska, F
      Alterations in fibrillin as well as collagens I and III and elastin occur in vulval lichen sclerosus

      JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
    11. Fietta, P; Manganelli, P
      Coexistent Marfan's syndrome and ankylosing spondylitis: A case report

      CLINICAL RHEUMATOLOGY
    12. Hanssen, E; Franc, S
      "Beads-on-a-string" filaments: structure, functions and associated pathologies

      M S-MEDECINE SCIENCES
    13. Di Lernia, V; Bonci, A; Cattania, M; Bisighini, G
      Striae distensae (rubrae) in monozygotic twins

      PEDIATRIC DERMATOLOGY
    14. 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
    15. Faury, G
      Function-structure relationship of elastic arteries in evolution: from microfibrils to elastin and elastic fibres

      PATHOLOGIE BIOLOGIE
    16. 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
    17. 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
    18. Oble, DA; Teh, HS
      Tight skin mouse subcutaneous hypertrophy can occur in the absence of up Tcell receptor-bearing lymphocytes

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

      JOURNAL OF RHEUMATOLOGY
    20. Gardella, R; Nuytinck, L; Barlati, S; Van Acker, P; Tadini, G; De Paepe, A; Colombi, M
      Characterization of mutations leading to recessive dystrophic epidermolysis bullosa and Marfan syndrome in a single patient

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    21. 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
    22. Akhtar, S; Bron, AJ; Meek, KM; Bennett, K
      Congenital hereditary endothelial dystrophy and band keratopathy in an infant with corpus callosum agenesis

      CORNEA
    23. 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
    24. 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
    25. 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
    26. 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
    27. Daamen, WF; Hafmans, T; Veerkamp, JH; van Kuppevelt, TH
      Comparison of five procedures for the purification of insoluble elastin

      BIOMATERIALS
    28. Salim, MA; Alpert, BS
      Sports and marfan syndrome - Awareness and early diagnosis can prevent sudden death

      PHYSICIAN AND SPORTSMEDICINE
    29. Ritch, R; Schlotzer-Schrehardt, U
      Exfoliation syndrome

      SURVEY OF OPHTHALMOLOGY
    30. Seo, JY; Lee, SH; Youn, CS; Choi, HR; Rhie, GE; Cho, KH; Kim, KH; Park, KC; Eun, HC; Chung, JH
      Ultraviolet radiation increases tropoelastin mRNA expression in the epidermis of human skin in vivo

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    31. 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
    32. Langenkamper, G; Manac'h, N; Broin, M; Cuine, S; Becuwe, N; Kuntz, M; Rey, P
      Accumulation of plastid lipid-associated proteins (fibrillin/CDSP34) upon oxidative stress, ageing and biotic stress in Solanaceae and in response todrought in other species

      JOURNAL OF EXPERIMENTAL BOTANY
    33. Koli, K; Saharinen, J; Karkkainen, M; Keski-Oja, J
      Novel non-TGF-beta-binding splice variant of LTBP-4 in human cells and tissues provides means to decrease TGF-beta deposition

      JOURNAL OF CELL SCIENCE
    34. 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
    35. Arteaga-Solis, E; Gayraud, B; Lee, SY; Shum, L; Sakai, L; Ramirez, F
      Regulation of limb patterning by extracellular microfibrils

      JOURNAL OF CELL BIOLOGY
    36. Baldock, C; Koster, AJ; Ziese, U; Rock, MJ; Sherratt, MJ; Kadler, KE; Shuttleworth, CA; Kielty, CM
      The supramolecular organization of fibrillin-rich microfibrils

      JOURNAL OF CELL BIOLOGY
    37. Kukuvitis, A; Georgiou, I; Ioannidis, S; Tarlatzis, B; Bontis, J; Papadimas, J
      Congenital obstructive azoospermia in a man with Marfan syndrome

      FERTILITY AND STERILITY
    38. 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
    39. 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
    40. Guo, DC; Hasham, S; Kuang, SQ; Vaughan, CJ; Boerwinkle, E; Chen, H; Abuelo, D; Dietz, HC; Basson, CT; Shete, SS; Milewicz, DM
      Familial thoracic aortic aneurysms and dissections - Genetic heterogeneitywith a major locus mapping to 5q13-14

      CIRCULATION
    41. 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
    42. 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
    43. Trask, BC; Broekelmann, T; Ritty, TM; Trask, TM; Tisdale, C; Mecham, RP
      Posttranslational modifications of microfibril associated glycoprotein-1 (MAGP-1)

      BIOCHEMISTRY
    44. 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
    45. 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
    46. Dodig, TD; Mack, KT; Cassarino, DF; Clark, SH
      Development of the tight-skin phenotype in immune-deficient mice

      ARTHRITIS AND RHEUMATISM
    47. van Karnebeek, CDM; Naeff, MSJ; Mulder, BJM; Hennekam, RCM; Offringa, M
      Natural history of cardiovascular manifestations in Marfan syndrome

      ARCHIVES OF DISEASE IN CHILDHOOD
    48. Alexiou, C; Langley, SM; Charlesworth, P; Haw, MP; Livesey, SA; Monro, JL
      Aortic root replacement in patients with Marfan's syndrome: The Southampton experience

      ANNALS OF THORACIC SURGERY
    49. Kitahama, S; Gibson, MA; Hatzinikolas, G; Hay, S; Kuliwaba, JL; Evdokiou, A; Atkins, GJ; Findlay, DM
      Expression of fibrillins and other microfibril-associated proteins in human bone and osteoblast-like cells

      BONE
    50. 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
    51. 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
    52. Oh, MR; Kim, JS; Beck, NS; Lee, HJ; Kohsaka, T; Jin, DK
      Six novel mutations of the fibrillin-1 gene in Korean patients with Marfansyndrome

      PEDIATRICS INTERNATIONAL
    53. Le Parc, JM; Molcard, S; Tubach, F; Boileau, C; Jondeau, G; Muti, C; Chevallier, B; Pisella, PJ
      Marfan syndrome and fibrillin disorders

      JOINT BONE SPINE
    54. Rose, PS; Levy, HP; Ahn, NU; Sponseller, PD; Magyari, T; Davis, J; Francomano, CA
      A comparison of the Berlin and Ghent nosologies and the influence of duralectasia in the diagnosis of Marfan syndrome

      GENETICS IN MEDICINE
    55. Fattori, R; Reggiani, LB; Pepe, G; Napoli, G; Bna, C; Celletti, F; Lovato, L; Gavelli, G
      Magnetic resonance imaging evaluation of aortic elastic properties as early expression of Marfan syndrome

      JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE
    56. Majors, AK; Pyeritz, RE
      A deficiency of cysteine impairs fibrillin-1 deposition: Implications for the pathogenesis of cystathionine beta-synthase deficiency

      MOLECULAR GENETICS AND METABOLISM
    57. Zhou, GM; Price, CE; Rosenquist, TH; Gadson, PF; Godfrey, M
      Partial cloning and sequencing of chick fibrillin-1 cDNA

      IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
    58. 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
    59. Guala, A; Danesino, C; Milewicz, DM; Putnam, EA; Franceschini, F
      The metacarpophalangeal profile in a family with congenital contractural arachnodactyly

      GENETIC COUNSELING
    60. McGettrick, AJ; Knott, V; Willis, A; Handford, PA
      Molecular effects of calcium binding mutations in Marfan syndrome depend on domain context

      HUMAN MOLECULAR GENETICS
    61. Ramirez, F
      Pathophysiology of the microfibril/elastic fiber system: introduction

      MATRIX BIOLOGY
    62. Handford, PA; Downing, AK; Reinhardt, DP; Sakai, LY
      Fibrillin: from domain structure to supramolecular assembly

      MATRIX BIOLOGY
    63. Milewicz, DM; Urban, Z; Boyd, C
      Genetic disorders of the elastic fiber system

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

      MATRIX BIOLOGY
    65. Berton, A; Godeau, G; Emonard, H; Baba, K; Bellon, P; Hornebeck, W; Bellon, G
      Analysis of the ex vivo specificity of human gelatinases A and B towards skin collagen and elastic fibers by computerized morphometry

      MATRIX BIOLOGY
    66. Frankfater, C; Maus, E; Gaal, K; Segade, F; Copeland, NG; Gilbert, DJ; Jenkins, NA; Shipley, JM
      Organization of the mouse microfibril-associated glycoprotein-2 (MAGP-2) gene

      MAMMALIAN GENOME
    67. 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
    68. Arteaga-Solis, E; Gayraud, B; Ramirez, F
      Elastic and collagenous networks in vascular diseases

      CELL STRUCTURE AND FUNCTION
    69. 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
    70. Fujimoto, N; Tajima, S; Ishibashi, A
      Expression of microfibril-associated glycoprotein-1 (MAGP-1) in human epidermal keratinocytes

      ARCHIVES OF DERMATOLOGICAL RESEARCH
    71. Ohnishi, Y; Tajima, S; Akiyama, M; Ishibashi, A; Kobayashi, R; Horii, I
      Expression of elastin-related proteins and matrix metalloproteinases in actinic elastosis of sun-damaged skin

      ARCHIVES OF DERMATOLOGICAL RESEARCH
    72. 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
    73. Dawson, PA; Marini, JC
      Hammerhead ribozymes selectively suppress mutant type I collagen mRNA in osteogenesis imperfecta fibroblasts

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

      ZEITSCHRIFT FUR KARDIOLOGIE
    75. Shipley, JM; Mecham, RP; Maus, E; Bonadio, J; Rosenbloom, J; McCarthy, RT; Baumann, ML; Frankfater, C; Segade, F; Shapiro, SD
      Developmental expression of latent transforming growth factor beta bindingprotein 2 and its requirement early in mouse development

      MOLECULAR AND CELLULAR BIOLOGY
    76. Oklu, R; Hesketh, R
      The latent transforming growth factor beta binding protein (LTBP) family

      BIOCHEMICAL JOURNAL
    77. Plantin, P; Durigon, M; Boileau, C; Le Parc, JM
      Fibrillin network in normal bone and cartilage

      ANNALES DE PATHOLOGIE
    78. Handford, PA
      Fibrillin-1, a calcium binding protein of extracellular matrix

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
    79. Tuling, JR; Crowther, ET; McCord, P
      Clinical considerations in the chiropractic management of the patient withMarfan syndrome

      JOURNAL OF MANIPULATIVE AND PHYSIOLOGICAL THERAPEUTICS
    80. Belleh, S; Zhou, GM; Wang, M; Der Kaloustian, VM; Pagon, RA; Godfrey, M
      Two novel fibrillin-2 mutations in congenital contractural arachnodactyly

      AMERICAN JOURNAL OF MEDICAL GENETICS
    81. Palz, M; Tiecke, F; Booms, P; Goldner, B; Rosenberg, T; Fuchs, J; Skovby, F; Schumacher, H; Kaufmann, UC; von Kodolitsch, Y; Nienaber, CA; Leitner, C; Katzke, S; Vetter, B; Hagemeier, C; Robinson, PN
      Clustering of mutations associated with mild Marfan-like phenotypes in the3 ' region of FBN1 suggests a potential genotype-phenotype correlation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    82. Sterzel, RB; Hartner, A; Schlotzer-Schrehardt, U; Voit, S; Hausknecht, B; Doliana, R; Colombatti, A; Gibson, MA; Braghetta, P; Bressan, GM
      Elastic fiber proteins in the glomerular mesangium in vivo and in cell culture

      KIDNEY INTERNATIONAL
    83. Pyeritz, RE
      The Marfan syndrome

      ANNUAL REVIEW OF MEDICINE
    84. Gerli, R; Solito, R; Weber, E; Agliano, M
      Specific adhesion molecules bind anchoring filaments and endothelial cellsin human skin initial lymphatics

      LYMPHOLOGY
    85. Abela-Formanek, C; Amon, M; Schauersberger, J; Schild, G; Kruger, A
      Postoperative inflammatory response to phacoemulsification and implantation of 2 types of foldable IOLs in pseudoexfoliation syndrome

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    86. Krumdieck, CL; Prince, CW
      Mechanisms of homocysteine toxicity on connective tissues: Implications for the morbidity of aging

      JOURNAL OF NUTRITION
    87. 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
    88. Robinson, PN; Godfrey, M
      The molecular genetics of Marfan syndrome and related microfibrillopathies

      JOURNAL OF MEDICAL GENETICS
    89. Duplan-Perrat, F; Damour, O; Montrocher, C; Peyrol, S; Grenier, G; Jacob, MP; Braye, F
      Keratinocytes influence the maturation and organization of the elastin network in a skin equivalent

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    90. Doliana, R; Canton, A; Bucciotti, F; Mongiat, M; Bonaldo, P; Colombatti, A
      Structure, chromosomal localization, and promoter analysis of the human elastin microfibril interfase located protein (EMILIN) gene

      JOURNAL OF BIOLOGICAL CHEMISTRY
    91. 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
    92. Pena, JDO; Mello, PAA; Hernandez, MR
      Synthesis of elastic microfibrillar components fibrillin-1 and fibrillin-2by human optic nerve head astrocytes in situ and in vitro

      EXPERIMENTAL EYE RESEARCH
    93. Kolker, SJ; Tajchman, U; Weeks, DL
      Confocal imaging of early heart development in Xenopus laevis

      DEVELOPMENTAL BIOLOGY
    94. 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
    95. 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
    96. 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
    97. 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
    98. Dingemans, KP; Teeling, P; Lagendijk, JH; Becker, AE
      Extracellular matrix of the human aortic media: An ultrastructural histochemical and immunohistochemical study of the adult aortic media

      ANATOMICAL RECORD
    99. Hinek, A; Zhang, SQ; Smith, AC; Callahan, JW
      Impaired elastic-fiber assembly by fibroblasts from patients with either Morquio B disease or infantile GM1-gangliosidosis is linked to deficiency inthe 67-kD spliced variant of beta-galactosidase

      AMERICAN JOURNAL OF HUMAN GENETICS
    100. Nakamura, M; Itoh, S; Makita, S; Ohira, A; Arakawa, N; Hiramori, K
      Peripheral resistance vessel dysfunction in Marfan syndrome

      AMERICAN HEART JOURNAL


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Documento generato il 11/08/20 alle ore 21:50:45