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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

New drugs targeting DNA enzymes show promise for cancer treatment but have side effects like immune system suppression and hair loss.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

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

ERG increases SOX9, promoting prostate cancer growth and invasion.

Small proline-rich proteins and trichohyalin help make epithelial tissues tougher and more flexible.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

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

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

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

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The KRTAP36-2 gene in sheep affects wool yield.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Lanceolate complexes in mouse hair follicles are essential for touch and depend on specific cells for maintenance and regeneration.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

The model accurately predicts age from saliva and buccal cells for forensic use.