Neurophysin in rats with hereditary hypothalamic diabetes insipidus (Brattleboro strain)

Characterization of prolactin and growth hormone immuno- and bioactivities in the pituitary gland and serum of the squirrel monkey (Saimiri boliviensis boliviensis).

American journal of primatology·2020

Studies on the structure and physiology of salmon teleocalcin.

Fish physiology and biochemistry·2013

Bromocriptine inhibits galanin gene expression in the rat pituitary gland.

Molecular and cellular neurosciences·2009

Endocrine communication between conceptus and mother: placental lactogen stimulation of maternal behavior.

Neuroendocrinology·1996

Plasma clearance, tissue uptake and expression of pituitary peptide 23/pancreatitis-associated protein in the rat.

The Journal of endocrinology·1995

Age-related changes in peptide-23/pancreatitis-associated protein and pancreatic stone protein/reg gene expression in the rat and regulation by growth hormone-releasing hormone.

Endocrinology·1995

BRN2 in Lineage Plasticity: A Prostate Cancer-Focused Perspective.

Endocrinology·2026

IL-22 Increases Proglucagon-expressing Enteroendocrine Cells via STAT3 in Human iPSC-derived Intestinal Epithelium.

Endocrinology·2026

Targeting Estrogen to the Brain via DHED does not seem to Protect Against Metabolic Dysfunction in Obese OVX Mice.

Endocrinology·2026

Hepatic Translational Rewiring in Insulin Deficiency Identifies Reg3α as an Insulin-Independent Glucoregulatory Factor.

Endocrinology·2026

Enhancer of zeste homolog 2 regulates B-cell responses in a NOD.H-2h4 model of spontaneous autoimmune thyroiditis.

Endocrinology·2026

Ligand-Induced Stability Studies at the TSH Receptor Show the Linking Region to be a Chameleon.

Endocrinology·2026

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Related Experiment Videos

Neurophysin in rats with hereditary hypothalamic diabetes insipidus (Brattleboro strain)

Related Concept Videos

Characterization of prolactin and growth hormone immuno- and bioactivities in the pituitary gland and serum of the squirrel monkey (Saimiri boliviensis boliviensis).

Studies on the structure and physiology of salmon teleocalcin.

Bromocriptine inhibits galanin gene expression in the rat pituitary gland.

Endocrine communication between conceptus and mother: placental lactogen stimulation of maternal behavior.

Plasma clearance, tissue uptake and expression of pituitary peptide 23/pancreatitis-associated protein in the rat.

Age-related changes in peptide-23/pancreatitis-associated protein and pancreatic stone protein/reg gene expression in the rat and regulation by growth hormone-releasing hormone.

BRN2 in Lineage Plasticity: A Prostate Cancer-Focused Perspective.

IL-22 Increases Proglucagon-expressing Enteroendocrine Cells via STAT3 in Human iPSC-derived Intestinal Epithelium.

Targeting Estrogen to the Brain via DHED does not seem to Protect Against Metabolic Dysfunction in Obese OVX Mice.

Hepatic Translational Rewiring in Insulin Deficiency Identifies Reg3α as an Insulin-Independent Glucoregulatory Factor.

Enhancer of zeste homolog 2 regulates B-cell responses in a NOD.H-2h4 model of spontaneous autoimmune thyroiditis.

Ligand-Induced Stability Studies at the TSH Receptor Show the Linking Region to be a Chameleon.

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Related Experiment Videos

Neurophysin in rats with hereditary hypothalamic diabetes insipidus (Brattleboro strain)

Related Concept Videos

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