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Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Runx3 helps determine hair shape.

Certain skin proteins can form anchoring structures without the protein AMACO.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

Targeting adipocyte-to-mesenchymal transition could help treat fibrosis.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

TBX3 gene affects pigmentation and marking formation in Dun Mongolian horses.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Monilethrix is a genetic hair disorder affecting hair shape, seen in two brothers.

Mutations in the SNRPE gene cause hereditary hair loss.

Skin organoids can regenerate hair by forming specific cell units with certain signals.

A rare benign tumor with hair follicle features was found on a man's trunk.

Brandt's hedgehog has thick skin on its back and many glands near its nostrils.

A man with a rare adrenal cancer showed unusual symptoms and died four months after diagnosis.

Monilethrix causes different levels of hair loss in family members.

The patient has a rare skin condition that shows features of two known disorders.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

Androgens in female meerkats influence aggression and dominance, affecting social dynamics and offspring behavior.

The research maps the complex development of early mouse skin, identifying diverse cell types and their roles in forming skin layers and structures.

Women with PCOS often have hirsutism and skin changes, which indicate a need for metabolic health checks.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

The interdigital gland of Vembur sheep shows sex-based differences in size and chemical makeup, possibly affecting communication and disease protection.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Adrenal tumors in hamsters are rare and hard to diagnose, highlighting the need for better diagnostic tools.

A single recessive gene causes sparse hair in certain Japanese White rabbits.

The FTO gene hinders stem cells in hair follicles from becoming pigment cells.