Results 81 to 90 of about 7,016 (204)

Intronic variant in POU1F1 associated with canine pituitary dwarfism. [PDF]

Hum Genet, 2021
Kyöstilä K, Niskanen JE, Arumilli M, Donner J, Hytönen MK, Lohi H.   +5 more
europepmc   +1 more source

Intrapituitary Regulatory System of Proliferation of Mammotrophs in the Pituitary Gland [PDF]

, 2004
Anterior pituitary cells produce growth factors plus cytokines and their receptors. Although some of these pituitary growth factors and cytokines are known to be involved in the control of cell differentiation, proliferation and hormone production in the
Takahashi, Sumio
core   +1 more source

Erratum to prostate biopsy free system for laparoscopic radical prostatectomy in a pituitary dwarfism: a case report. [PDF]

Transl Androl Urol, 2021
Editorial Office.
europepmc   +1 more source

Restored vision in a young dog following corticosteroid treatment of presumptive hypophysitis [PDF]

, 2016
Background: Hypophysitis is an umbrella term for a group of disorders involving inflammation of the pituitary gland. A rare occurrence in humans, hypophysitis can produce a range of clinical signs including (but not limited to) visual deficits and ...
Liuti, Tiziana, Marioni-Henry, Katia, Rzechorzek, Nina Marie, Stalin, Catherine   +3 more
core   +2 more sources

PACAP induces FSHβ gene expression via EPAC. [PDF]

, 2019
Gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), are heterodimers of a common α subunit and unique β subunits. Regulation of their levels, primarily by GnRH, is critical for reproductive function.
Coss, Djurdjica, Yeh, Debra M
core  

A point mutation in the AF-2 domain of thyroid hormone receptor alpha1 expressed after CRE mediated recombination partially recapitulates hypothyroidism. [PDF]

, 2007
Thyroid hormones act directly on transcription by binding to TRα1, TRβ1, TRβ2 nuclear receptors, regulating many aspects of post-natal development and homeostasis.
Flamant, Frederic, Quignodon, Laure, Samarut, Jacques, Vincent, Séverine, Winter, Harald   +4 more
core   +1 more source

A new locus for Seckel syndrome on chromosome 18p11.31-q11.2 [PDF]

, 2001
Seckel syndrome (MIM 210600) is a rare autosomal recessive disorder with a heterogeneous appearance. Key features are growth retardation, microcephaly with mental retardation, and a characteristic 'bird-headed' facial appearance.
Balslev, Thomas, Binderup, Helle Glud, Birkebaek, N, Børglum, Anders, Haagerup, Annette, Hertz, Jens Michael, Kruse, T A   +6 more
core   +1 more source

Hypothalamic-Pituitary Functions in Patients with Idiopathic Pituitary Dwarfism

Endocrinologia Japonica, 1975
To investigate hypothalamic-pituitary functions and the primary site of the lesion in idiopathic pituitary dwarfism, various pituitary function tests, especially the pituitary hormone responses to the hypophysiotropic hormones were studied in 23 patients with idiopathic pituitary dwarfism.
R, Demura, K, Jujo, K, Takano, E, Odagiri, T, Maeda, T, Suda, H, Demura, K, Shizume   +7 more
openaire   +3 more sources

Growth Performance, Feed Intake and vegf121 Gene Expression Feature of Dwarf Cyprinus carpio rubrofuscus

Progress in Fishery Sciences
To explore the molecular mechanism of dwarf fish formation in the cultured population of Cyprinus carpio rubrofuscus and the functions of vascular endothelial growth factor (VEGF) in fish growth, the features of growth trait, feed intake, and feed ...
Shuozhen CHEN, Dongmei MA, Zaixuan ZHONG, Jiajia FAN, Huaping ZHU, Huanhuan SU   +5 more
doaj   +1 more source

О подходах к сохранению доступности лекарственной помощи отдельным категориям граждан Российской Федерации [PDF]

, 2014
Нормативные документы, регламентирующие предоставление гражданам России дорогостоящих лекарственных препаратов. Результаты изучения мнения пациентских организаций и медицинских работников об их уровне доступности для населения.
Мошкова, Л. В., Рейхтман, Т. В.   +1 more
core   +1 more source