Results 51 to 60 of about 7,504 (217)
Diagnostics(1) Background: Pituitary adenomas are benign tumors comprising about 18% of all intracranial tumors, and they often require surgical intervention. Differentiating pituitary tissue from adenoma during surgery is crucial to minimize complications.
Tomislav Felbabić +2 more
doaj +1 more source
Isotocin Regulates Growth Hormone but Not Prolactin Release From the Pituitary of Ricefield Eels
Frontiers in Endocrinology, 2018 The neurohypophyseal hormone oxytocin (Oxt) has been shown to stimulate prolactin (Prl) synthesis and release from the adenohypophysis in rats. However, little is known about the functional roles of Oxt-like neuropeptides in the adenohypophysis of non ...
Wei Yang +7 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Aicardi–Goutières syndrome type 6 (AGS6) is a genetically determined autoinflammatory disorder, classically inherited in an autosomal recessive manner. We report a Czech child with a heterozygous ADAR1 NM_001111.5:c.3019G>A variant causing AGS6.
Katerina Turan +11 more
wiley +1 more source
Acta Physiologica, Volume 242, Issue 4, April 2026.ABSTRACT Thyroid hormones (THs) are under negative feedback regulation via the hypothalamic–pituitary‐thyroid (HPT) axis. How this axis operates to keep the circulating THs within a narrow physiological range is not well understood quantitatively. Led by the design principle of robust homeostatic feedback control, here we review and synthesize the ...
Li Jing, Sarahna A. Moyd, Qiang Zhang
wiley +1 more source
, 1974 In addition to confirming the reports by McEwen and co-workers of a selective uptake of corticosterone by the dorsal hippocampus in adrenalectomized rats, our findings have brought to light an inverse relationship between corticosterone retention by the
Edouard Bastarache +4 more
core +1 more source
Lymphocitic infundibuloneurohypophysitis mimicking a pituitary adenoma
Clinics and Practice, 2011 A rare case of infundibulo-neurohypophysitis mimicking a pituitary adenoma is presented. A 69-years-old female patient developed polyuria and polydipsia. Laboratory analysis revealed central diabetes insipidus. No hormonal abnormalities. Cranial-magnetic
Lorenzo Giammattei +3 more
doaj +1 more source
ISOLATED GROWTH HORMONE DEFICIENCY – A RARE, BUT TREATABLE CAUSE OF LOW STATURE [PDF]
Romanian Journal of Pediatrics, 2019 Growth hormone deficiency is a rare cause of low stature. Early recognition of the disease results in effective treatment, leading to a final height as closely as possible to the genetic target.
Raluca Maria Vlad +2 more
doaj +1 more source
Veterinary Medicine and Science, Volume 12, Issue 2, March 2026.ABSTRACT Background The sella turcica is an important skull formation due to its close anatomical relationship with the pituitary gland. Therefore, the shape and morphometry of the sella turcica provide crucial preliminary information for the determination of cases.
Sedat Aydoğdu, Yusuf Altundağ
wiley +1 more source
BMP4 and FGF strongly induce differentiation of mouse ES cells into oral ectoderm
Stem Cell Research, 2015 During embryonic development, oral ectoderm differentiates into the adenohypophysis, dental epithelia, salivary glands, and nasal pit. Few reports exist concerning the induction of oral ectoderm from embryonic stem (ES) cells.
Hiroshi Ochiai +12 more
doaj +1 more source
The Anatomical Record, Volume 309, Issue 1, Page 201-213, January 2026.Abstract Neuroanatomy studies in vertebrates have garnered significant attention in recent years, particularly driven by advancements in computerized tomography imaging techniques. Nonetheless, these advancements remain largely constrained to specific vertebrate groups, notably mammals, birds, and fish, leaving studies in reptiles at an incipient stage.
Giordanna Issa Lucas, Angele Martins
wiley +1 more source