Results 121 to 130 of about 26,437 (217)

Neurofibroma of Lip: Report of a Rare Case

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2010
Neurofibroma is a benign tumor of neural tissue origin. It most frequently involves the skin and rarely the oral mucosa. The nature of the disease has been recognized as hereditary with an autosomal dominant trait with variable penetrance.
N Kannan   +2 more
doaj  

Diagnostic and therapeutic process of neurofibromatosis type 1 and type 2

open access: yesJournal of Education, Health and Sport
Neurofibromatosis is one of the most common genetic diseases. It is inherited in an autosomal dominant manner. It is divided into two genetically distinct subtypes, characterised by multiple skin lesions and tumours of the peripheral and central nervous 
Michał Leśniewski   +3 more
doaj   +1 more source

Updated nomenclature for human and mouse neurofibromatosis type 1 genes [PDF]

open access: yes, 2017
Anastasaki, Corina   +3 more
core   +2 more sources

Genetic requirement for Ras in the transformation of fibroblasts and hematopoietic cells by the Bcr-Abl oncogene. [PDF]

open access: yes, 1995
To determine the functional importance of Ras in transformation by Abl oncogenes, we used a genetic approach to measure the effect of impaired Ras activity on the ability of Bcr-Abl or v-Abl to transform cells.
McLaughlin, J, Sawyers, CL, Witte, ON
core  

Effects of Methyl Cycle Substrate Availability on Epigenetic Stability of Human Embryonic Stem Cells [PDF]

open access: yes
A link has been hypothesised to occur between suboptimal maternal nutrition and impaired foetal development leading to a predisposition to a range of adult pathologies.
Barsanti, Marco
core  

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