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Stem and progenitor cells in the eye have different division rates and locations, affecting how they respond to injury.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The scalp has a natural speckled pattern of increased pigment around hair follicles, possibly linked to local hormone production.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

A new genetic mutation was found causing hair and eye issues in a boy.

Entrepreneurial companies are key to advancing dermatology treatments and patient care.

The research found that androgens help control blood flow in the rat prostate through a specific binding site.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Feather pigment patterns form through melanocyte arrangement and simple regulatory mechanisms.

Brindled mice show abnormal catecholamine neuron development due to copper deficiency.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

A 22-year-old's gray hair partially turned back to its original color without known causes.

Pigmented rings with central clearing help diagnose melasma more accurately.

New genetic variants linked to albinism were found in Pakistani families.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

A rare, harmless hair condition was found in an infant's eyebrow, needing no treatment.

PmtHEE is a better model for studying pigmented skin because it includes melanocytes and shows improved cell differentiation.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Only skin melanocytes, not other types, can color hair in mice.

Hair splitting and nail detachment are linked conditions.

Tiger tail bands in hair are caused by wavy hair fibers with melanin, unlike straight fibers in normal hair.

ChromaLens offers more precise and stable hair coloring than traditional methods.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.