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Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Disulfide bonds make keratin in hair stronger and tougher.

Mouse genital development depends on male or female hormones for specific features.

Cat claws stay sharp by shedding their outer layer through microcracks formed during activities.

Estrogen can temporarily slow down hair growth but this can be reversed.

Fatp4 is crucial for healthy skin development and function.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The right amount of retinoic acid is essential for normal hair growth and development.

TGase 3 helps build hair structure by forming strong bonds between proteins.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Different fields of expertise must work together to better understand hair growth and create effective hair loss treatments.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Epidermal stem cells create and maintain skin structures like hair and nails through specific signaling pathways and vary by location and function.

Zinc pyrithione needs targeted delivery to the scalp for effective dandruff treatment.

Activating Nrf2 in skin cells speeds up wound healing by increasing the growth of certain stem cells.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

Melatonin could be an effective treatment for Alzheimer's Disease and rosacea.

A specific gene mutation causes Olmsted syndrome.

Keratin filaments' elasticity is influenced by their terminal domains and surrounding medium.

Disulfide bonds in keratin fibers break more easily under stress, especially when wet, affecting fiber strength.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.