Results 71 to 80 of about 2,445,354 (228)

SHP-2 deletion in postmigratory neural crest cells results in impaired cardiac sympathetic innervation [PDF]

open access: yes, 2014
Autonomic innervation is an essential component of cardiovascular regulation that is first established from the neural crest (NC) lineage in utero and continues developing postnatally.
Conway, Simon J.   +5 more
core   +2 more sources

Assessing the Drivers of Distribution for a Cryptic Species Over a Large and Rugged Landscape: Occupancy Modeling of the Critically Endangered Northern White‐Cheeked Gibbon

open access: yesEcology and Evolution, Volume 16, Issue 1, January 2026.
We conducted presence/non‐detection sampling of the Critically Endangered northern white‐cheeked gibbon in Lao PDR. Occupancy was found to be a function of human usage of the site, distance from the nearest road, and the uninterruptedness of forest cover.
Jay White   +3 more
wiley   +1 more source

Prevalence of myocarditis and its contribution to the course of primary myocardial hypertrophy

open access: yesРоссийский кардиологический журнал, 2023
Aim. To assess the incidence of myocarditis in patients with primary myocardial hypertrophy and to study its contribution to the disease course.Material and methods. The study included 100 patients with primary left ventricular myocardial hypertrophy, 52
Yu. A. Lutokhina   +6 more
doaj   +1 more source

The likely effects of thermal climate change on vertebrate skeletal muscle mechanics with possible consequences for animal movement and behaviour [PDF]

open access: yes, 2019
Climate change can involve alteration in the local temperature that an animal is exposed to, which in turn may affect skeletal muscle temperature.
Abrahams   +100 more
core   +1 more source

Phosphatase-independent functions of SHP2 and its regulation by small molecule compounds

open access: yesJournal of Pharmacological Sciences, 2020
SHP2 is a non-receptor protein tyrosine phosphatase encoded by the PTPN11 gene in human. Clinically, SHP2 has been identified as a causal factor of several diseases, such as Noonan syndrome, LEOPARD syndrome as well as myeloid malignancies. Interestingly,
Wenjie Guo, Qiang Xu
doaj   +1 more source

Nanoporous silica-based protocells at multiple scales for designs of life and nanomedicine. [PDF]

open access: yes, 2015
Various protocell models have been constructed de novo with the bottom-up approach. Here we describe a silica-based protocell composed of a nanoporous amorphous silica core encapsulated within a lipid bilayer built by self-assembly that provides for ...
Brinker, C Jeffrey   +3 more
core   +2 more sources

Advances in pancreatic cancer early diagnosis, prevention, and treatment: The past, the present, and the future

open access: yesCA: A Cancer Journal for Clinicians, Volume 76, Issue 1, January/February 2026.
Abstract Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with a dismal prognosis, largely because of late‐stage diagnosis and therapeutic resistance. PDAC incidence has been rising, with modifiable and non‐modifiable risk factors contributing to disease development.
Alessandro Mannucci, Ajay Goel
wiley   +1 more source

Hypertrophic cardiomyopathy in an adult patient with Noonan syndrome with multiple lentigines

open access: yesClinical Case Reports, 2023
Key Clinical Message Noonan syndrome with multiple lentigines (NSML) is a rare RASopathy caused by pathogenic variants (PV) predominantly in PTPN11 gene.
Pamela Rivero‐García   +2 more
doaj   +1 more source

Relationship between aetiology and left ventricular systolic dysfunction in hypertrophic cardiomyopathy. [PDF]

open access: yes, 2017
BACKGROUND: Severe left ventricular (LV) systolic dysfunction is an uncommon complication of hypertrophic cardiomyopathy (HCM) that is associated with poor prognosis.
Biagini   +22 more
core   +2 more sources

LEOPARD syndrome in an infant with severe hypertrophic cardiomyopathy and PTPN11 mutation

open access: yesAnnals of Pediatric Cardiology, 2011
In LEOPARD syndrome, mutations affecting exon 13 of the PTPN11 gene have been correlated with a rapidly progressive severe biventricular obstructive hypertrophic cardiomyopathy (HCM).
Ganigara Madhusudan   +2 more
doaj  

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