Basic and clinical aspects of non-neuronal acetylcholine: biological and clinical significance of non-canonical ligands of epithelial nicotinic acetylcholine receptors

SA Grando - Journal of pharmacological sciences, 2008 - Elsevier
Mucocutaneous keratinocytes and bronchial epithelial cells express nicotinic acetylcholine
receptors (nAChRs). Emerging evidence indicates that nAChRs can be stimulated also by …

Mal de Meleda: a focused review

C Perez, A Khachemoune - American journal of clinical dermatology, 2016 - Springer
Mal de Meleda is a rare autosomal recessive palmoplantar keratoderma (PPK) disease with
an estimated prevalence of 1: 100,000. Clinically, the onset of the disease is typically soon …

Inherited disorders of cornification

V Oji, D Metze, H Traupe - Rook's Textbook of Dermatology …, 2016 - Wiley Online Library
The majority of keratinization disorders are referred to as Mendelian disorders of
cornification. This is a very broad group, clinically characterized by hyperkeratosis or visible …

[HTML][HTML] Endogenous CHRNA7-ligand SLURP1 as a potential tumor suppressor and anti-nicotinic factor in pancreatic cancer

VM Throm, D Männle, T Giese, AS Bauer, MM Gaida… - Oncotarget, 2018 - ncbi.nlm.nih.gov
Smoking is associated with increased risk and poorer prognosis of pancreatic ductal
adenocarcinoma (PDAC). Nicotine acts through cholinergic nicotinic receptors, preferentially …

SLURP‐1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene

C Bergqvist, H Kadara, L Hamie… - International journal …, 2018 - Wiley Online Library
Abstract Background Mal de Meleda (MDM) is a rare inherited autosomal recessive
genodermatosis characterized by palmoplantar keratoderma (PPK) with transgrediens and …

SLURP1 mutation‐impaired T‐cell activation in a family with mal de Meleda

JW Tjiu, PJ Lin, WH Wu, YP Cheng… - British Journal of …, 2011 - academic.oup.com
Summary Background Mal de Meleda (MDM) is palmoplantar erythrokeratoderma with an
autosomal recessive inheritance and is caused by a mutation in the gene encoding SLURP …

Comparative proteomic analysis of matched primary and metastatic melanoma cell lines

M Al-Ghoul, TB Brück, JL Lauer-Fields… - Journal of proteome …, 2008 - ACS Publications
Identification of the biochemical pathways involved in the transformation from primary to
metastatic melanoma is an area under intense investigation. A 2DE proteomics approach …

Papillon-Lefèvre syndrome and malignant melanoma: a high incidence of melanoma development in Japanese palmoplantar keratoderma patients

K Nakajima, H Nakano, N Takiyoshi, A Rokunohe… - Dermatology, 2008 - karger.com
Papillon-Lefèvre syndrome (PLS) is a rare autosomal-recessive genodermatosis
characterized by palmoplantar hyperkeratosis and severe early-onset periodontitis. The …

Overexpression of SLURP-1 and-2 alleviates the tumorigenic action of tobacco-derived nitrosamine on immortalized oral epithelial cells

J Arredondo, AI Chernyavsky, SA Grando - Biochemical pharmacology, 2007 - Elsevier
Recent research has demonstrated that mucocutaneous epithelial cells express functional
nicotinic acetylcholine receptors (nAChRs) and that tobacco-derived carcinogenic …

Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region

M Bchetnia, N Laroussi, M Youssef… - BioMed Research …, 2013 - Wiley Online Library
Mal de Meleda (MDM) is a rare, autosomal recessive form of palmoplantar keratoderma. It is
characterized by erythema and hyperkeratosis of the palms and soles that progressively …