نتایج جستجو برای: stachys laxa

تعداد نتایج: 1261  

Journal: :In vivo 2005
Adam Gbankoto Jean Vigo Karim Dramane Bernard Banaigs Eustache Aina Jean-Marie Salmon

Laxaphycin A (laxa A) and Laxaphycin B (laxa B), cyclic peptides isolated from the terrestrial blue-green alga Anabaena laxa or the marine cyanobacterium Lyngbya majuscula have antifungal and cytotoxic activities. We used numerical videomicrofluorometry and a protocol of multiple labelling with Hoescht 33342 (nuclear DNA), Rhodamine 123 (mitochondria) and Nile Red (plasma membrane) to study the...

2003
E. Radnai Á. Dobos K. Veres L. Tóth

The volatile oil compositions of five Stachys species (Stachys officinalis L., St. grandiflora Host., St. byzantina Koch., St. germanica L. and St. sylvatica L.) have been studied using a GC/MS technique. All species gave low yields of oil. From St. officinalis 38 compounds were separated and partly identified, from St. grandiflora 24, St. byzantina 30, St. germanica 29 and St. sylvatica 43. Al...

2014
Mojgan Mohammadi

Stachys genus with medicinal properties and high polymorphic features has been considered one of the largest genera of Lamiaceae. The aim of this study was to determine the flavonoid pattern variations and flavonoid groups in ten Stachys species belonging to two sections; Fragilicaulis, and Aucheriana. The studied species were collected from natural habitats in Iran and analysed for their flavo...

2015
Bagher Minae Mehdi Sardari Hossein Sharifi Massih Sedigh Rahim Abadi Omid Sadeghpour

CONTEXT In modern phytotherapy, Stachys lavandulifolia Vahl., a type of Stachys also known as Mountain Tea (Chay-e-Kouhi) has been widely studied based on its botanical and therapeutic characteristics over the recent decades. EVIDENCE ACQUISITION The present study investigated morphology, botanical characteristics, and some therapeutic activities of this plant and compares them with those of ...

Journal: :Molecular phylogenetics and evolution 2015
Tilottama Roy Logan W Cole Tien-Hao Chang Charlotte Lindqvist

The phenomenon of polyploidy and hybridization usually results in novel genetic combinations, leading to complex, reticulate evolution and incongruence among gene trees, which in turn may show different phylogenetic histories than the inherent species tree. The largest tribe within the subfamily Lamioideae (Lamiaceae), Stachydeae, which includes the globally distributed Stachys, and one of the ...

2017
Ariana Kariminejad Fariba Afroozan Bita Bozorgmehr Alireza Ghanadan Susan Akbaroghli Hamid Reza Khorram Khorshid Faezeh Mojahedi Aria Setoodeh Abigail Loh Yu Xuan Tan Nathalie Escande-Beillard Fransiska Malfait Bruno Reversade Thatjana Gardeitchik Eva Morava

Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autosomal recessive cutis laxa syndromes, namely cutis laxa IIA (ARCL2A), cutis laxa IIB (ARCL2B), and geroderma osteodysplastica (GO), have very similar...

Journal: :Journal of medical genetics 2006
Z Szabo M W Crepeau A L Mitchell M J Stephan R A Puntel K Yin Loke R C Kirk Z Urban

BACKGROUND Cutis laxa is an acquired or inherited condition characterized by redundant, pendulous and inelastic skin. Autosomal dominant cutis laxa has been described as a benign disease with minor systemic involvement. OBJECTIVE To report a family with autosomal dominant cutis laxa and a young girl with sporadic cutis laxa, both with variable expression of an aortic aneurysmal phenotype rang...

2009
Franco Piozzi Maurizio Bruno

The occurrence of diterpenoids in the essential oils of the species of the genus Stachys (Lamiaceae, Labiatae) is reviewed.

Journal: :Human molecular genetics 2002
Bart Loeys Lionel Van Maldergem Geert Mortier Paul Coucke Sabine Gerniers Jean-Marie Naeyaert Anne De Paepe

Hereditary cutis laxa comprises a heterogeneous group of connective tissue disorders characterized by loose skin and variable systemic involvement. Autosomal dominant and recessive as well as X-linked forms have been described. Some dominant forms are caused by mutations in the elastine gene (ELN). The X-linked form is now classified in the group of copper transport diseases. The genetic defect...

2013
Mehdi Alehossein Masoud Pourgholami Kamyar Kamrani Mohammad Soltani Afshin Yazdi Payman Salamati

Cutis laxa (CL) is a rare congenital and acquired disorder characterized by loose and redundant skin with reduced elasticity. Three types of congenital cutis laxa have been recognized. Other findings are pulmonary emphysema, bronchiectasia, hernia and diverticulosis. We describe a female neonate involved by cutis laxa syndrome and a positive family history. We focus on the radiologic findings o...

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