Zobrazeno 1 - 10
of 909
pro vyhledávání: '"Lamina densa"'
Autor:
Janina Müller-Deile, Victoria Rose, Jan Hegermann, Christoph Daniel, Kerstin Amann, Marwin Gröner, Mario Schiffer, Nina Sopel, Alexandra Ohs, Christoph Wrede, Gunther Zahner
Publikováno v:
J Am Soc Nephrol
Background Autoantibodies binding to podocyte antigens cause idiopathic membranous glomerulonephritis (iMGN). However, it remains elusive how autoantibodies reach the subepithelial space because the glomerular filtration barrier (GFB) is size selecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1c808ba1e58f1854cc5584bc3252156
https://doi.org/10.1681/asn.2020121699
https://doi.org/10.1681/asn.2020121699
Publikováno v:
Acta Histochemica et Cytochemica
The basement membrane (BM)-related factors, including collagen IV, are important for the maintenance and recovery of skeletal muscles. Aging impairs the expression of BM-related factors during recovery after disuse atrophy. Muscle activity facilitate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::056141bd118ec838abe7f06b5155dee0
https://doi.org/10.1267/ahc.21-00057
https://doi.org/10.1267/ahc.21-00057
Publikováno v:
Neonatology, surgery and perinatal medicine. 10:87-91
Summary. Hereditary bullous epidermolysis (BE) is a group of genetically and clinically heterogeneous diseases characterized by the formation of blisters and erosion due to injury on the skin and mucous membranes. Different forms of BE can be accompa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c208850b2337f2ea132afe477b59877c
https://doi.org/10.24061/2413-4260.x.4.38.2020.10
https://doi.org/10.24061/2413-4260.x.4.38.2020.10
Autor:
Gobinda Chatterjee, Keya Basu, Raghavendra Rao, Abhishek De, Manimoy Bandopadhyay, Subhrajyoti Karmakar
Publikováno v:
International Journal of Clinical and Diagnostic Pathology. 3:461-468
Background: Epidermolysis Bullosa is a rare genetic mechanobullous skin and mucosal fragility with blistering. It is classified into: Epidermolysis (Simplex), lucidolytic (Junctional) and dermolytic (Dystrophic). The disease is extremely debilitating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c94ace7f24693a13ce342c180699cf
https://doi.org/10.33545/pathol.2020.v3.i1g.212
https://doi.org/10.33545/pathol.2020.v3.i1g.212
Autor:
M.A. de Laat, Christopher C. Pollitt
Publikováno v:
Domestic Animal Endocrinology. 69:30-34
The third phalanx of the equine digit is suspended within the hoof capsule by a specialized interdigitating dermoepidermal layer called the lamellae, which fails during laminitis. Pathology of the basement membrane (BM), which interfaces epidermis an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1220547947544394d3af5bdf348bf34b
https://doi.org/10.1016/j.domaniend.2019.04.004
https://doi.org/10.1016/j.domaniend.2019.04.004
Autor:
Luciane Donida Bartoli Miot, Daniela Carvalho dos Santos, Hélio Amante Miot, Ana Cláudia Cavalcante Espósito, Gabrielli Brianezi, Nathália Pereira de Souza
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2020-12-12T01:42:44Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-04-01 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a29ff8153e98483d24c2d772c420382a
https://doi.org/10.1007/s00403-019-01979-w
https://doi.org/10.1007/s00403-019-01979-w
Autor:
Ariana Kariminejad, Keith A. Choate, John A. McGrath, Alyson Guy, Mahtab Naji, Leila Youssefian, Masoud Zabihi, Nailah Harvey, Lynn M. Boyden, Andrew Touati, Sirous Zeinali, Hassan Vahidnezhad, Amir Hossein Saeidian, Lu Liu, Soheila Sotoudeh, Mohammadreza Barzegar, Jouni Uitto
Publikováno v:
Matrix biology : journal of the International Society for Matrix Biology. 99
Epidermolysis bullosa (EB) is a genotypically heterogeneous group of disorders characterized by cutaneous blistering and erosions with a tremendous spectrum of severity. One of the distinct forms of EB, Kindler EB (KEB), manifests with blistering and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f45ed7c09db9223a2984ac187049d2f
https://pubmed.ncbi.nlm.nih.gov/34004352
https://pubmed.ncbi.nlm.nih.gov/34004352
Accepted manuscript version, licensed CC BY-NC-ND 4.0. The muscle cells and extracellular matrices (ECMs) of two teleost-infecting blood flukes belonging to distinct evolutionary lineages of the Aporocotylidae (Digenea) were examined using Transmissi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed34a836bcfad6cc8f0cce8463e61150
https://hdl.handle.net/10037/25138
https://hdl.handle.net/10037/25138
Autor:
Richard Viebahn, Dierk Gruhn, Gianluca Ciardelli, Valeria Chiono, Inge Schmitz, Alice Zoso, Sandra Pacharra, S. Shah, Jochen Salber, Ayesha Idrees
Publikováno v:
4 open, Vol 4, p 1 (2021)
Nowadays, human skin constructs (HSCs) are required for biomaterials, pharmaceuticals and cosmeticsin vitrotesting and for the development of complex skin wound therapeutics.In vitrothree-dimensional (3D) dermal-epidermal based interfollicular, full-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9d824b419ecfd09fb450e7e23260819
https://www.4open-sciences.org/articles/fopen/full_html/2021/01/fopen200025/fopen200025.html
https://www.4open-sciences.org/articles/fopen/full_html/2021/01/fopen200025/fopen200025.html
Autor:
Kelly D. Smith, Fuki M. Hisama, Christopher D. Blosser, Jennifer Schleit, Michael O. Dorschner, Nicole K. Andeen
Publikováno v:
American Journal of Kidney Diseases. 72:296-301
Variants in the LMX1B gene cause nail-patella syndrome, a rare autosomal dominant disorder characterized by dysplasia of nails, patella and elbow abnormalities, iliac "horns," and glaucoma. We describe an adult man with nephrotic syndrome and no syst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2c8a9090b528ca37d28896b3aff1af
https://doi.org/10.1053/j.ajkd.2017.09.023
https://doi.org/10.1053/j.ajkd.2017.09.023