نتایج جستجو برای: leopard syndrome

تعداد نتایج: 623523  

Journal: :Indian Journal of Paediatric Dermatology 2018

اسمعیلی, سعیده, سفیانیان, علیرضا , همامی, محمود‌رضا ,

Distribution modelling is important for assessing threats and conservation status of species and for planning conservation programs. We studied the distribution of suitable habitats of Asiatic cheetah (Acinonyx jubatus venaticus), Persian leopard (Panthera pardus saxicolor) and brown bear (Ursus arctos) in Isfahan province within and outside the protected areas. Suitable habitats of the three s...

Journal: :environmental resources research 2014
davoud fadakar hamid reza rezaei majid hosseini sayyad sheikhy ilanloo wahid zamani

the leopard (panthera pardus) as an adaptable felid widely distributed in varied ecosystems of iran. the golestan natural park is one of the main habitats of leopard in the country. it has divers diet and preying various types of preys such as wild ungulate and livestock. the prey remains’ samples of leopard were collected and preserved using ethanol 96% and whole genomic dna was extracted. the...

2017
Alireza Tafazoli Peyman Eshraghi Zahra Kamel Koleti Mohammadreza Abbaszadegan

Noonan syndrome (NS) is an autosomal dominant disorder with vast heterogeneity in clinical and genetic features. Various symptoms have been reported for this abnormality such as short stature, unusual facial characteristics, congenital heart abnormalities, developmental complications, and an elevated tumor incidence rate. Noonan syndrome shares clinical features with other rare conditions, incl...

2015
Marianna Spatola Christian Wider Thierry Kuntzer Alexandre Croquelois

BACKGROUND LEOPARD syndrome (LS) belongs to the family of neuro-cardio-facio-cutaneous syndromes, which include Neurofibromatosis-1 (NF1), Noonan syndrome, Costello Syndrome, cardio-facio-cutaneous syndrome, Noonan-like syndrome with loose anagen hair and Legius syndrome. These conditions are caused by mutations in genes encoding proteins involved in the RAS-MAPK cellular pathway. Clinical hete...

2011
Xia Liu Cheng-Kui Qu

SHP-2 (PTPN11), a ubiquitously expressed protein tyrosine phosphatase, is critical for hematopoietic cell development and function owing to its essential role in growth factor/cytokine signaling. More importantly, germline and somatic mutations in this phosphatase are associated with Noonan syndrome, Leopard syndrome, and childhood hematologic malignancies. The molecular mechanisms by which SHP...

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