Results 81 to 90 of about 2,763 (196)

Extracellular Matrix Origin Directs Morphogenesis and Gene Regulation in Bioengineered Human Skin

Advanced Healthcare Materials, Volume 15, Issue 15, 17 April 2026.
Fibroblast‐driven production of endogenous extracellular matrix is shown to be essential for guiding transcriptional programs and morphogenesis in biofabricated human skin equivalents. Constructs relying on native, cell‐produced ECM support physiological dermo‐epidermal junction formation and tissue architecture, whereas exogenous matrices promote ...
Francesco Galardo, Giorgia Imparato, Costantino Casale, Francesco Urciuolo, Luca Mannino, Antonio Federico, Dario Greco, Paolo Antonio Netti   +7 more
wiley   +1 more source

Junctional epidermolysis bullosa, non-Herlitz type

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2018
La epidermólisis ampollosa de las uniones (JEB, por sus siglas en inglés) es una enfermedad ampollosa de la piel hereditaria de forma recesiva y es causada por anomalías en las proteínas que retienen las capas de la piel. Herlitz JEB es la forma severa y no Herlitz JEB es la forma más leve.
Munir Ahmad Bhinder, Muhammad Arshad, Muhammad Yasir Zahoor, Wasim Shehzad, Muhammad Tariq, Muhammad Imran Shabbir   +5 more
openaire   +2 more sources

Complete Paternal Uniparental Isodisomy of Chromosome 1: A Novel Mechanism for Herlitz Junctional Epidermolysis Bullosa

, 2000
Uniparental disomy denotes a situation when an individual has inherited two copies of a specific chromosome from a single parent. Uniparental disomy has been demonstrated to be involved in the pathogenesis of recessively inherited diseases in rare cases.
Nakajima, Hiromichi, Takizawa, Yasuko, Nakano, Yasushi, Uitto, Jouni, Chao, Sheau-Chiou, Pulkkinen, Leena, Shimizu, Hiroshi   +6 more
core   +1 more source

Aplasia Cutis Congenita in Bart's Syndrome: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Aplasia cutis congenita (ACC) is a partial or complete absence of skin layers which can be a part of a syndromic disease. Bart's syndrome is a combination of clinical manifestations including ACC, epidermolysis bullosa, blistering in the oral mucosa, nail dystrophy, or congenital absence of nails. Additional anomalies, such as pyloric atresia,
Parvaneh Sadeghimoghadam, Niloofar Hoorshad, Maryam Ghavami Adel, Mahroo Rezaeinejad, Marjan Ghaemi   +4 more
wiley   +1 more source

Occurrence of epidermolysis bullosa along with Amelogenesis imperfecta in female patient of India

Dental Research Journal, 2013
Epidermolysis bullosa (EB) is an inherited disorder, which is characteristically presented as skin blisters developing in response to minor injury. Junctional variety of EB is also associated with enamel hypoplasia.
A P Javed, Prashanth Shenai, Laxmikanth Chatra, K M Veena, Prasanna Kumar Rao, Rachana Prabhu   +5 more
doaj   +1 more source

Localized epidermolysis bullosa simplex with generalized enamel hypoplasia in a child

, 2006
Epidermolysis bullosa is an uncommon disease characterized by the formation of blisters following minor trauma. The three major types are simplex, junctional, and dystrophic.
HATİPOĞLU, HASAN, Hatipoglu, MG, ÇAĞIRANKAYA, LEYLA BERNA   +2 more
core   +2 more sources

(New) antenatal ultrasound signs of fetal junctional epidermolysis bullosa: A case report and systematic review of literature

, 2023
20.500.12530/87857Epidermolysis bullosa is a rare hereditary autosomal disease that is included in the heterogeneous group of genodermatosis. It is characterized by skin and mucous membranes fragility and denudation, and it can be associated with pyloric
Josè Luis Bartha, Valentina Tosto, Raul de Lucas, Bartha, Josè Luis, Eugenia Antolin, Barbara Moreno-Sanz, Tamara Illescas, Herrero, Beatriz, de Lucas, Raul, Illescas, Tamara, Beatriz Herrero, Moreno-Sanz, Barbara, Tosto, Valentina, De la Calle Fernandez-Miranda, Maria, Maria De la Calle Fernandez-Miranda, Antolin, Eugenia   +15 more
core   +1 more source

Inherited epidermolysis bullosa: Case report of finger localization

Indian Journal of Plastic Surgery, 2012
Inherited epidermolysis bullosa is a rare condition that often present at birth with skin blisters and erosions. They are associated with defective cohesion of the dermis and epidermis. There are 3 principal types: Simple, junctional and dystrophic.
Anne- Aurore Sankale, Ndeye Coulibaly, Lamine Ndiaye, Hugues Tiemdjo   +3 more
doaj   +1 more source

Junctional and Dystrophic Epidermolysis Bullosa

, 2013
Epidermolysis bullosa (EB) is a congenital genodermatosis, which affects mainly skin and occasionally other organs [1]. Lifelong blistering and erosion of the skin and mucous membrane, caused by mechanical trauma, threaten EB patients [1]. The most common cause of death is metastasizing squamous cell carcinoma [2].
Daisuke Tsuruta, Chiharu Tateishi, Masamitsu Ishii   +2 more
openaire   +2 more sources

Genética Molecular das Epidermólises Bolhosas Molecular Genetics of Epidermolysis Bullosa

Anais Brasileiros de Dermatologia, 2002
O estudo das alterações moleculares das epidermólises bolhosas tem contribuído para que se compreenda melhor essas enfermidades. Na epidermólise bolhosa simples a maioria dos casos está associada com alteração nas citoqueratinas basais 5 (gen KRT5) e 14 (
Hiram Larangeira de Almeida Jr
doaj   +1 more source