Results 61 to 70 of about 7,016 (204)

Dwarfism in beef cattle and the influence of dwarfism genes on physiological response to hormone-induced stress [PDF]

open access: yes, 1961
This bulletin reports on Department of Animal Husbandry research project 198, 'Improvement of Beef Cattle Through Breeding'--P. [2].Digitized 2007 AES.Includes bibliographical references (pages 50-55)
Comfort, James E. (James Edwin), 1899-   +2 more
core  

PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency [PDF]

open access: yes, 2006
OBJECTIVE: Mutations of the PROP1 gene lead to combined pituitary hormone deficiency (CPHD), which is characterized by a deficiency of GH, TSH, LH/FSH, PRL and, less frequently, ACTH.
Agapito, A   +12 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

Marfan syndrome and pituitary dwarfism [PDF]

open access: yesJapanese Journal of Human Genetics, 1981
A very rare case with Marfan syndrome born from his mother with Marfan syndrome and his father with pituitary dwarfism (type I) was described. In the maternal families the consanguinity and Marfan syndrome were present. In the paternal families the consanguinity and dwarfism were present.
openaire   +2 more sources

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

Abnormal corticosterone regulation in an immature rat model of continuous chronic stress. [PDF]

open access: yes, 1996
Neuroendocrine correlates of chronic stress in human infants have not been established. The goal of the present study was to create an animal model of continuous chronic stress using the immature rat to measure basal plasma corticosterone, and secretion ...
Baram, TZ, Gilles, EE, Schultz, L
core   +2 more sources

ATRX: From Chromatin Remodeling to Disease

open access: yesgenesis, Volume 63, Issue 6, December 2025.
ABSTRACT Chromatin remodeling proteins are evolutionarily conserved factors involved in a wide range of biological processes. In this review, we describe ATRX, a chromatin remodeling protein belonging to the SWI/SNF2 family. Its association with different protein complexes, and its roles in embryonic development, sexual differentiation, as well as ...
Mauro Magaña‐Acosta   +1 more
wiley   +1 more source

Neurotransmitters and Immunity: Molecular Mechanisms, Biological Functions, Diseases, and Potential Therapeutic Targets

open access: yesMedComm, Volume 6, Issue 12, December 2025.
Role of neurotransmitters in multiple pathological processes. Various neurotransmitters, including ACh, EPI, NE, 5‐HT, histamine, DA, glutamate, GABA, and neuropeptides participate in regulating key pathological events, including tumor proliferation, tumor migration, remodeling of the immune microenvironment, and the development of NDDs and ...
Gege Li   +13 more
wiley   +1 more source

Differential Tissue Response to Growth Hormone in Mice [PDF]

open access: yes, 2018
Growth hormone (GH) has been shown to act directly on multiple tissues throughout the body. Historically, it was believed that GH acted directly in the liver and only indirectly in other tissues via insulin‐like growth hormone 1 (IGF‐1).
Banerjee, Ronadip R.   +4 more
core   +2 more sources

A Case of CSNK2A1 Gene Variant Causing Okur‐Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum

open access: yesMolecular Genetics &Genomic Medicine, Volume 13, Issue 12, December 2025.
In the present study, a de novo variant of the CSNK2A1 gene, designated c.149A>G (p.Tyr50Cys), was identified in a subject diagnosed with OCNDS by WES. The molecular mechanism by which this variant leads to a wide range of clinical phenotypes by disrupting the kinase domain function was elucidated through a combination of experimental investigation and
Xin Li   +6 more
wiley   +1 more source

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