Results 111 to 120 of about 135,933 (247)

Non-beta-cell progenitors in pregnant mice and the origin and functionality of beta-cells after diabetic recovery in a c-Myc ablation model [PDF]

open access: yes
The debate regarding the contribution of adult stem/progenitor cells during normal growth and beta-cell regeneration is far from being resolved. Therefore, we addressed in two distinct situations the origin of new beta-cells.
Abouna, Sylvie
core  

Unique Inflammatory Changes in Exocrine and Endocrine Pancreas in Enterovirus-induced Fulminant Type 1 Diabetes

open access: yes, 2019
Context: There is scant report on the pathological changes of the exocrine and endocrine pancreas in fulminant type 1 diabetes mellitus (FT1DM). Objective: To clarify the distinct pathological changes in the exocrine as well as the endocrine pancreas ...
Youichi Oikawa (6291486)   +9 more
core   +2 more sources

Exocrine pancreatic insufficiency at diabetes mellitus

open access: yesРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии, 2009
The aim of review. To give the characteristic of exocrine pancreatic insufficiency in diabetes mellitus (DM).Original positions. Exocrine function of the pancreas is reduced in 40–80% of patients with insulindependent and in 15–73% of patients with 2nd ...
N. B. Gubergrits   +2 more
doaj  

Successful use of insect‐based (Hermetia illucens) diet in dogs with food‐responsive enteropathy

open access: yesJournal of Small Animal Practice, EarlyView.
Objective Diet is an integral component of the management of chronic enteropathy in dogs. The role of insect‐based diets in this disease remains unknown. The objective of this study was to evaluate the impact of an insect‐based (Hermetia illucens) diet in dogs with presumed food‐responsive enteropathy.
K. Murtagh   +4 more
wiley   +1 more source

Ion Channel Dysfunction and Therapeutic Targeting in Salivary Gland Disorders

open access: yesOral Diseases, EarlyView.
ABSTRACT Objective Salivary gland hypofunction and xerostomia represent major clinical complications of radiation therapy, autoimmune disorders such as Sjögren's disease, and inherited epithelial ion transport defects. This review integrates current knowledge on ion channel dysfunction as a central mechanistic driver of salivary gland pathology and ...
Tarek Mohamed Abd El‐Aziz   +6 more
wiley   +1 more source

11C-Hydroxytryptophan uptake and metabolism in endocrine and exocrine pancreas [PDF]

open access: yes, 2012
Determination of the residual beta-cell mass using noninvasive tools might help to follow up the efficacy of new treatments in both type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus, including islet transplantation.
Dierckx, Rudi A. J. O.   +12 more
core   +2 more sources

Analytical Validation of an Automated Point‐of‐Care Immunoassay for the Measurement of Canine Pancreatic Lipase Immunoreactivity Concentration (Vcheck cPL 2.0)

open access: yesVeterinary Clinical Pathology, EarlyView.
ABSTRACT Background Pancreatic lipase assays are commonly utilized in the diagnostic approach to suspected pancreatitis in dogs. While a previously available point‐of‐care assay for the quantification of canine pancreatic lipase immunoreactivity (Vcheck cPL 1.0) performed sub‐optimally, the updated version (Vcheck cPL 2.0) lacks independent validation.
Isabel Mendoza‐White   +2 more
wiley   +1 more source

Evaluation of Additional Treatment for Residual Cases After Endoscopic Papillectomy of Duodenal Ampullary Tumors

open access: yesDEN Open, Volume 7, Issue 1, April 2027.
ABSTRACT Background and Aims This study aimed to assess the prognosis and outcomes of additional treatment for residual adenocarcinoma and adenoma following endoscopic papillectomy (EP) for ampullary tumors. Methods Of 191 patients who underwent EP, 43 with adenocarcinoma or adenoma and either positive or unknown pathological margins were included ...
Yusuke Kurita   +24 more
wiley   +1 more source

Neuropsychological and Educational Outcomes in Shwachman–Diamond Syndrome—A Report From the North American Shwachman–Diamond Syndrome Registry

open access: yesPediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
ABSTRACT Background Shwachman–Diamond syndrome (SDS) is a rare autosomal recessive ribosomopathy characterized by bone marrow failure and multisystem involvement, with emerging evidence of associated neurocognitive impairment. Methods We conducted a retrospective study of 240 individuals with biallelic Shwachman–Bodian–Diamond syndrome (SBDS) mutations
Jane Koo   +11 more
wiley   +1 more source

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