Results 61 to 70 of about 4,412 (188)

Juvenile hyposomatotropism in a Somali cat presenting with seizures due to intermittent hypoglycaemia

open access: yesJournal of Feline Medicine and Surgery Open Reports, 2018
Case summary A 3-month-old intact male Somali cat was evaluated for a history of seizures, hypoglycaemia and mental dullness 4 weeks after being bitten in the head by a dog.
Maya Laura König   +3 more
doaj   +1 more source

Relationship Between Gut Microbiota and Cancer Neuro‐Immunity

open access: yesMicrobial Biotechnology, Volume 19, Issue 3, March 2026.
Tumour cells influence neural activity and microbiota homeostasis through cytokines and immune modulation. Meanwhile, gut microbiota regulates neural function through metabolic products, affects immune responses via neurotransmitters, feedback regulates neural activity and influences tumour microenvironment.
Danyang Wang   +7 more
wiley   +1 more source

Circulating Profiles of the Bile Acid Metabolomics in Patients With Polycystic Ovary Syndrome Treated With Metformin or Canagliflozin

open access: yesPharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, Volume 46, Issue 2, February 2026.
ABSTRACT Objective Bile acids are indispensable modulators in the development of polycystic ovary syndrome (PCOS). Our previous study identified that metformin and canagliflozin have similar efficacy in patients with PCOS combined with insulin resistance (IR).
Qi Yan   +8 more
wiley   +1 more source

Genetic interaction between the homeobox transcription factors HESX1 and SIX3 is required for normal pituitary development [PDF]

open access: yes, 2008
Hesx1 has been shown to be essential for normal pituitary development. The homeobox gene Six3 is expressed in the developing pituitary gland during mouse development but its function in this tissue has been precluded by the fact that in the Six3 ...
Gaston-Massuet, Carles   +8 more
core   +1 more source

Aldehyde Dehydrogenase 2 Gene Polymorphism and Alcohol Consumption Are Associated With Nephrolithiasis in a Chinese Population

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
ALDH2 polymorphisms are associated with increased risk of nephrolithiasis in humans, and Aldh2 deficiency promotes kidney stone formation in mice, especially under alcohol exposure. ABSTRACT Background Nephrolithiasis is a common urological disorder and has become a significant global public health issue.
Tao Liu   +11 more
wiley   +1 more source

Transient dwarfism and hypogonadism in mice lacking Otx1 reveal prepubescent stage-specific control of pituitary levels of GH, FSH and LH [PDF]

open access: yes, 1998
Genetic and molecular approaches have enabled the identification of regulatory genes critically involved in determining cell types in the pituitary gland and/or in the hypothalamus.
J. J. Tremblay   +6 more
core  

Inherited ateliotic dwarfism in mice. Characteristics of the mutation, little, on chromosome 6. [PDF]

open access: yes, 1976
A new autosomal recessive mutation in the mouse, little (lit), has been shown to be located on Chromosome 6. The mutation in the homozygous state causes ateliotic dwarfism that is first detected at 15 days of age by decreased body weight.
Eicher, E M, Beamer, W G
core  

The gatekeepers of growth: The neural roles and regulation of growth hormone‐releasing hormone neurons

open access: yesJournal of Neuroendocrinology, Volume 38, Issue 1, January 2026.
Abstract The neuroendocrine control of growth is mediated by the hypothalamic–pituitary–somatic (HPS) axis. This involves the hypothalamic release of growth hormone‐releasing hormone (GHRH), which stimulates the pituitary secretion of growth hormone (GH).
Bradley B. Jamieson
wiley   +1 more source

TREATMENT OF IDIOPATHIC PITUITARY DWARFlSM WITH HUMAN GROWTH HORMONE [PDF]

open access: yes, 1989
Clinical study of human growth hormone (hGH) treatment for 12 patients with idiopathic pituitary dwarfism is reported. In eleven out of 12 patients treated with hGH, growth rate was significantly increased. There was no significant difference between the
上田, 直子   +11 more
core  

Familial combined pituitary hormone deficiency by a mutation in PROP1: 4 of 7 brothers affected [PDF]

open access: yes, 2016
IntroductionPROP1 (Prophet of POUF1) mutations are the most frequent genetic cause of combined pituitary hormone deficiency, a condition associated with a deficiency or inadequate production of hormones of the anterior pituitary. The PROP1 gene encodes a
Carvalho, Davide   +4 more
core   +1 more source

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