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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Activin A and follistatin control when hair cells develop in mouse ears.

Activin A and follistatin control when ear hair cells form in mice.

Activin A promotes ear hair cell development, while follistatin delays it.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Selective Androgen Receptor Modulators (SARMs) are drugs that can control the effects of androgens in different tissues, potentially having fewer side effects and promising for treating various conditions.

Keratin from hair and wool is used in medical materials for healing and drug delivery.

The Hairless gene is crucial for healthy skin and hair growth.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

A special receptor in sensory nerve endings helps control how they respond to stretching.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

HOXC13 is essential for hair and nail development by regulating Foxn1.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

Researchers found new potential treatments for conditions related to the androgen receptor, like male hormonal contraception, by testing thousands of compounds.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Reductive stress messes up collagen balance and alters cell signaling in human skin cells, which could help treat certain skin diseases.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.