Results 81 to 90 of about 1,207 (150)

Desmosomal Molecules In and Out of Adhering Junctions: Normal and Diseased States of Epidermal, Cardiac and Mesenchymally Derived Cells [PDF]

, 2010
Current cell biology textbooks mention only two kinds of cell-to-cell adhering junctions coated with the cytoplasmic plaques: the desmosomes (maculae adhaerentes), anchoring intermediate-sized filaments (IFs), and the actin microfilament-anchoring ...
Barth, Mareike, Franke, Werner W., Pieperhoff, Sebastian, Rickelt, Steffen   +3 more
core   +3 more sources

The potency of the fs260 connexin43 mutant to impair keratinocyte differentiation is distinct from other disease-linked connexin43 mutants [PDF]

Although there are currently 62 mutants of Cx43 (connexin43) that can cause ODDD (oculodentodigital dysplasia), only two mutants have also been reported to cause palmar plantar hyperkeratosis.
Ajani, Alao, Baden, Beyer, Bragg, Braun-Falco, Chopra, Choudhry, Dale W. Laird, Das, de Carvalho, de Zwart-Storm, Flenniken, Gillespie, Goliger, Goliger, Gong, Gong, Goodenough, Guo, Gutmann, Gutstein, Iossa, Jared M. Churko, Kelly, Kimonis, Kimyai-Asadi, Kjaer, Kretz, Lai, Laird, Langlois, Langlois, Li, Maass, Maestrini, Masgrau-Peya, McLachlan, Musil, Nagasawa, Paznekas, Petit, Qing Shao, Richard, Richards, Rouan, Scherer, Simek, Stephanie Langlois, Thomas, Uyguner, Vanslyke, van Steensel, Vreeburg, White, Xinyue Pan   +55 more
core   +2 more sources

Molecular Genetics of Keratinization Disorders - What\u27s New About Ichthyosis [PDF]

, 2020
The heritable forms of keratinization disorders, including various forms of ichthyosis and keratodermas, comprise a phenotypically heterogeneous group of diseases which can be divided into syndromic and non-syndromic forms.
Saeidian, Amir Hossein, Uitto, Jouni, Vahidnezhad, Hassan, Youssefian, Leila   +3 more
core   +1 more source

Punctate palmoplantar keratoderma type I: the clinical and genetic features of two family members with AAGAB gene mutation

Revista da Sociedade Portuguesa de Dermatologia e Venereologia
Hereditary punctate palmoplantar keratoderma type I (PPPK1) is a rare autosomal dominant disorder characterized by hyperkeratotic papules on the palms and soles, typically appearing in adolescence but occasionally manifesting later in life.
Lanyu Sun, Leonor Lopes, Pedro Vasconcelos, Luís Soares-de-Almeida, Gabriel Miltenberger-Miltenyi, Joana F. Ferreira, Paulo Filipe   +6 more
doaj  

Pitted Plaques of Palms and Soles [PDF]

Porokeratosis is a chronic and progressive disorder of keratinization. Punctate porokeratosis is grossly described as multiple minute keratotic projections over the palmoplantar region.
Akshata Mane, Akshay Arvind Patankar, Mahesh Unni, Priyanka Sunil Malhotra, Purvesh Fale   +4 more
core   +1 more source

Tratamiento queratodermias palmoplantares [PDF]

, 2014
Treball Final de Grau de Podología, Escola Universitaria d'Infermeria, Universitat de Barcelona, curs: 2013-2014, Tutor: Antonio ZalacainLas patologías dermatológicas que cursan con trastornos en la producción de queratina son patologías muy habituales ...
Araguas Garcia, Caleb
core  

Towards a comprehensive resource for elucidating the pathogenesis of inherited keratodermas [PDF]

, 2010
Keratoderma – pathological hyperkeratosis of palms and soles - is a cause of disability in many clinical situations, including the rare and heterogeneous group of inherited palmoplantar keratodermas (PPKs).
Zamiri, Mozheh
core  

Hereditary Palmoplantar Keratosis [PDF]

, 2013
Kawakami, Tamihiro
core   +1 more source

Hypopigmentation-punctate palmoplantar keratoderma syndrome [PDF]

, 2020
openaire   +1 more source

Punctate palmoplantar keratoderma type 1 [PDF]

, 2020
openaire   +1 more source