Results 11 to 20 of about 207,485 (334)

Case report: Successful treatment of a rare case of combined parathyroid adenoma, cervical bronchogenic cyst, and tracheal diverticulum with gasless endoscopic resection of neck masses via an axillary approach: A case report and literature review

open access: yesFrontiers in Oncology, 2022
Parathyroid adenoma (PA), one of the most common causes of hyperparathyroidism, generally involves a single parathyroid gland and is manifested as hyperparathyroidism.
Dong-Ning Lu   +7 more
doaj   +1 more source

Investigating the Association Between rs2439302 Polymorphism and Thyroid Cancer: A Systematic Review and Meta-Analysis

open access: yesFrontiers in Surgery, 2022
Background and AimsThe extent of surgical treatment for most patients with thyroid cancer (TC) remains controversial and varies widely. As an emerging technology, genetic testing facilitates tumor typing and disease progression monitoring and is expected
Yawen Guo   +11 more
doaj   +1 more source

A Systematic Pan-Cancer Analysis of CASP3 as a Potential Target for Immunotherapy

open access: yesFrontiers in Molecular Biosciences, 2022
CASP3 is the gene encoding caspase-3, a specific protease that cleaves substrates such as poly-ADP ribose polymerase and acetyl-DEVD-7-amino-4-methylcoumarin. This enzymatic activity leads to DNA fragmentation, which is a hallmark of apoptosis.
Zheng Zhou   +9 more
doaj   +1 more source

Level II lateral neck dissection for papillary thyroid carcinoma: A retrospective cohort study

open access: yesAsian Journal of Surgery, 2023
Background: For N1b papillary thyroid carcinoma (PTC) patients, lateral neck dissection encompassing levels Ⅱ-Ⅴ is generally recommended. However, routine level Ⅱ dissection is controversial given the low incidence of metastasis, and potential ...
Tian Lv   +8 more
doaj   +1 more source

Genetic regulation of pituitary gland development in human and mouse [PDF]

open access: yes, 2009
Normal hypothalamopituitary development is closely related to that of the forebrain and is dependent upon a complex genetic cascade of transcription factors and signaling molecules that may be either intrinsic or extrinsic to the developing Rathke’s ...
Aarskog   +321 more
core   +2 more sources

Timing of maternal exposure and fetal sex determine the effects of low-level chemical mixture exposure on the fetal neuroendocrine system in sheep [PDF]

open access: yes, 2016
We have shown that continuous maternal exposure to the complex mixture of environmental chemicals (ECs) found in human biosolids (sewage sludge), disrupts mRNA expression of genes crucial for development and long-term regulation of hypothalamo-pituitary ...
Bellingham, M.   +7 more
core   +2 more sources

Ligula intestinalis (Cestoda: Pseudophyllidea): an ideal fish-metazoan parasite model? [PDF]

open access: yes, 2010
Since its use as a model to study metazoan parasite culture and in vitro development, the plerocercoid of the tapeworm, Ligula intestinalis, has served as a useful scientific tool to study a range of biological factors, particularly within its fish ...
Carter, V, Dufour, S, Hoole, D
core   +1 more source

Multiple endocrine neoplasia type 4: a new member of the MEN family

open access: yesEndocrine Connections, 2023
Objective: Multiple endocrine neoplasia type 4 (MEN4) is caused by a CDKN1B germline mutation first described in 2006. Its estimated prevalence is le ss than one per million. The aim of this study was to define the disease characteristics.
Hélène Singeisen   +9 more
doaj   +1 more source

Is There a Causal Association between Genotoxicity and the Imposex Effect? [PDF]

open access: yes, 2006
There is a growing body of evidence that indicates common environmental pollutants are capable of disrupting reproductive and developmental processes by interfering with the actions of endogenous hormones.
Colborn T   +13 more
core   +2 more sources

A late diagnosis of MEN 1 Syndrome in a young patient initially pre-senting with nephrolithiasis

open access: yesLiječnički vjesnik, 2023
Multiple Endocrine Neoplasms Type 1 (MEN 1), originally called Wermer Syndrome, is a rare hereditary condition caused by mutations in the MEN1 tumor suppressor gene.
Ana Čala, Tina Dušek
doaj   +1 more source

Home - About - Disclaimer - Privacy