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The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Women with idiopathic hirsutism and PCOS have higher RBP4 levels, and PCOS is linked to greater insulin resistance; weight management may help both conditions.

The therapies improved ejaculation disorders and sexual function in middle-aged men.

Calorie restriction boosts stem cell activity, improving tissue regeneration and lifespan.

RORA may help regulate hair growth by affecting hair follicle stem cells.

Cuscuta reflexa leaves extract may help lower blood sugar and improve diabetes symptoms.

CLE14 peptide promotes root hair growth in Arabidopsis.

The skin produces and responds to thyroid-stimulating hormone, which is controlled by other thyroid-related hormones.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Obese and non-obese women with PCOS have higher heart risk markers, especially if they are obese.

Skin symptoms like fragile skin and easy bruising can indicate Cushing's syndrome, which requires early diagnosis and treatment to prevent serious health issues.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Children with classic congenital adrenal hyperplasia have thicker heart fat and more heart and blood vessel risk factors, especially if their condition is not well-controlled.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Oestrogen and thyrotropin-releasing hormone affect prolactin and its receptor in human skin and hair, suggesting new treatment options for related conditions.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

BRG1 is essential for skin cells to move and heal wounds properly.

Children with classic congenital adrenal hyperplasia have thicker heart fat and are at higher risk for heart problems and early atherosclerosis.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

CRET therapy affects inflammation in skin cells by changing cytokine levels and activating certain proteins.

Hair cortisol levels decrease as children age, stabilizing around age 4.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

The Chinese version of the PCOS quality of life questionnaire is reliable and valid for Chinese-speaking women with PCOS.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.