Endogenous opiates block dopamine inhibition of prolactin secretion in vitro

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Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations.

The Journal of clinical endocrinology and metabolism·2011

[Genetic aspects of growth hormone deficiency].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie·2011

The gsp oncogene disrupts Ras/ERK-dependent prolactin gene regulation in gsp inducible somatotroph cell line.

Endocrinology·2011

Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms.

European journal of endocrinology·2011

RET gene mutations are not involved in the origin of human testicular seminoma.

International journal of andrology·2010

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Integrated signatures define mutational processes in prostate cancer.

Nature·2026

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Nature·2026

Imaging cellular activity across all organs reveals body-wide circuits.

Nature·2026

Neocortical long-range inhibition promotes cortical synchrony and sleep.

Nature·2026

TRI-611, a selective, brain-penetrant molecular glue degrader of ALK.

Nature·2026

Brixadi for Stimulant Use Disorder: Evolving Pharmacologic Considerations and Clinical Implications.

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Current clinical applications and future developments of platinum-based anticancer drugs.

Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry·2026

Evaluating clinical characteristics and outcomes associated with body stuffers presenting to the emergency department: a five-year retrospective analysis from a United States poison center.

Clinical toxicology (Philadelphia, Pa.)·2026

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Chemistry & biodiversity·2026

Real-Life Application of the Penicillin Allergy Decision Rule (PEN-FAST) Score in De-Labeling Penicillin Allergy: A Case Series.

Cureus·2026

Outcomes From the Use of Cefazolin for Surgical Prophylaxis in Patients Allergic to Penicillin.

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Phenotypic homogeneity and genotypic variability in a large series of congenital isolated ACTH-deficiency patients with TPIT gene mutations.

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