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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Wnt1/βcatenin signaling is crucial for heart repair after injury.

A protein from certain immune cells is key for new hair growth after skin injury in mice.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The guidelines suggest a detailed approach to diagnosing and treating lupus, with a focus on regular check-ups, personalized medicine, and a range of drug options for different cases.

Noggin is necessary to start the hair growth phase in skin after birth.

Overexpression of activin A in mice skin causes skin thickening, fibrosis, and improved wound healing.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Finasteride treats enlarged prostate and may help with baldness, but effects on sexual function and male fetuses are unclear.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

Blocking COX, especially COX-2, in the skin can reduce inflammation and pain and may help prevent skin cancer.

CDP is crucial for lung and hair follicle cell development.

Certain inhibitors slow down plant growth by causing early cell specialization without changing the cell development pattern.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

Different types of stem cells in hair follicles play unique roles in wound healing and hair growth, with some stem cells not originating from existing hair follicles but from non-hair follicle cells. WNT signaling and the Lhx2 factor are key in creating new hair follicles.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

About 2.2% of women with symptoms of high male hormones have a mild form of congenital adrenal hyperplasia, and measuring a specific hormone level can accurately diagnose it.

Cathepsin L is essential for normal hair growth and development.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.