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Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Aging-related hormone changes affect voice quality, especially during puberty, menstruation, pregnancy, and menopause.

The essay suggests hair loss might be caused by changes in skull bones.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Chicken feather growth involves specific genes and shares similarities with hair development.

The Wnt/β-catenin pathway is important for tissue development and has potential in regenerative medicine, but requires more research for therapeutic use.

HSPGs help control stem cell behavior, affecting hair growth and offering a target for hair loss treatments.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Some cosmetics and dermatological drugs can cause allergic reactions and side effects, like skin irritation and systemic issues.

Micrografts are useful for healing wounds, regenerating bone and periodontal tissues, and improving hair transplantation outcomes.

Scientists are using clumps of special stem cells to improve organ repair.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Androgens affect bone and fat cell development differently based on the cells' embryonic origin.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Ezh2 controls skin development by balancing signals for dermal and epidermal growth.

Pilose antler extracts help hair growth by activating hair follicle stem cells.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Finasteride improves immune response and reduces organ damage after trauma hemorrhage in mice.