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MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Changthangi goats have specific genes that help produce Pashmina wool.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

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

Animal models have helped understand hair loss from alopecia areata and find new treatments.

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

Certain signals and genes play a key role in hair growth and regeneration, and understanding these could lead to new treatments for skin regeneration.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Early-stage skin cells help regenerate hair follicles, with proteins SDF1, MMP3, biglycan, and LTBP1 playing key roles.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Sonic hedgehog proteins may help grow hair.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

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

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Stress hormone corticosterone blocks a growth factor to slow down hair stem cell activity and hair growth.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Glutathione helps Arabidopsis roots adapt to low phosphate by regulating a specific growth pathway.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.