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ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

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

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

The enzymes 5α-reductase and 3α/β-hydroxysteroid oxidoreductase help create brain-active substances from progesterone and testosterone, which could be used for treatment, but more research is needed to ensure their safety and effectiveness.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The Wnt/β-catenin pathway helps tissue regeneration but can also cause fibrosis, and drugs that inhibit this pathway may aid in healing skin and heart tissues.

A group has developed therapies that show promise for treating cancer and various other conditions.

New genes found linked to balding, may help develop future treatments.

Wnt signaling is crucial for skin development and hair growth.

Hair color is determined by melanin produced and transferred in hair follicles.

The document concludes that blocking the internal pathways that create androgens might help treat cancers that depend on sex hormones.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Melatonin may protect ear cells from damage caused by nicotine.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Fetal hair follicles have melanocytes with melanosomes at different stages, which are broken down into pigment particles in keratinocytes.

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

FP-1 is a key protein in rat hair growth, active only during the growth phase.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Two distinct pathways direct proteins to vacuoles in Arabidopsis, affecting root hair growth and protein targeting.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Tissue-derived extracellular vesicles are crucial for cancer diagnosis, prognosis, and treatment.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.