Results 1 to 10 of about 6,050 (216)

A missense mutation in the KCNE4 gene is not predictive of equine anhidrosis. [PDF]

Anim Genet
Anhidrosis is defined as a decreased or absent ability to sweat in response to heat and exercise. In horses, this condition can increase the risk of life-threatening hyperthermia.
Brown, Briana, Finno, Carrie, Leigh, Wesley, Petersen, Jessica, Roberts, Kelsey, Ryan, Stephanie, Szmatoła, Tomasz, Van Buren, Samantha, van der Graaf, Lexie   +8 more
core   +3 more sources

Miliaria and Anhidrosis

Journal of Investigative Dermatology, 1967
Ever since the investigations of Robinson (1), Pollitzer (2) and Schlachta (3), it has been accepted that all forms of miliaria are associated with occlusion of the outlets of the eccrine sweat glands followed by an inability of the affected gland to deliver sweat to the surface.
Tommy B. Griffin, Tommy B. Griffin, Howard I. Mailbach, Marion B. Sulzberger   +3 more
  +7 more sources

Studies on the Mechanism of Aluminum Anhidrosis*

Journal of Investigative Dermatology, 1968
Hydroxyethyleellulose 0.3% Water 93.7% The test agent was applied to the forearm twice daily without occlusion for four days, the other forearm acting as a control. On the fifth day 0.1 ml of 1: 1,000 methacholine (Meeholyl®) was injected intradermally in both forearms as a sweat stimulator; sweat rates were recorded for 15 minutes with a modified ...
Bernard I. Gordon, Howard I. Maibach
openaire   +4 more sources

Acquired idiopathic generalized anhidrosis [PDF]

Journal of Dermatological Case Reports, 2014
Anhidrosis is a failure in sweat production in response to physiological thermal or chemical stimuli. Acquired idiopathic generalized anhidrosis is a rare disorder without sweat gland pathology and without neurologic symptoms. Most cases have been reported from Far East.
Uwe Wollina
openaire   +4 more sources

Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): Mutations and polymorphisms inTRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor

Human Mutation, 2001
Yasuhiro Indo
exaly   +2 more sources

Congenital insensitivity to pain with anhidrosis (CIPA): Novel mutations of theTRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutantTRKA andPKLR genes in a family with CIPA and pyruvate kinase deficiency

Human Mutation, 2001
Generoso Andria
exaly   +2 more sources

Clinical and genetic analysis of ERCC8-Related cockayne syndrome: hepatic dysfunction as a biomarker, anhidrosis as a rare feature, and rehabilitation outcomes for ankle contractures [PDF]

Front Genet
Jing Chen, Chi‐Wei Su, Danying Gao, Fangfang Liu, Shuang Chen, Wenhan Zhang, Min Peng, Tao Lei, Hongmin Zhu   +8 more
openalex   +2 more sources

The structure of latherin, a surfactant allergen protein from horse sweat and saliva [PDF]

, 2013
Latherin is a highly surface-active allergen protein found in the sweat and saliva of horses and other equids. Its surfactant activity is intrinsic to the protein in its native form, and is manifest without associated lipids or glycosylation.
Alan Cooper, Brian O. Smith, Lamping N, Malcolm W. Kennedy, Rhona E. McDonald, Steven J. Vance, Vance SJ   +6 more
core   +1 more source

Plasma catecholamines, sweat electrolytes and physiological responses of exercised normal, partial anhidrotic and anhidrotic horses [PDF]

, 2009
Problem statement: Malaysia imports horses from temperate countries to develop equine sports in the country. Several of these horses developed partial and complete anhidrosis.
Abdullah, Rasedee, Fateh Mohamed, Bashir Ahmad   +1 more
core   +1 more source

The Israeli National Genetic database: a 10-year experience [PDF]

, 2017
BACKGROUND: The Israeli National and Ethnic Mutation database ( http://server.goldenhelix.org/israeli ) was launched in September 2006 on the ETHNOS software to include clinically relevant genomic variants reported among Jewish and Arab Israeli patients.
Patrinos, G.P. (George P.), Zlotogora, J. (Joël)   +1 more
core   +8 more sources