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Researchers found two genes that may explain why some Casertana pigs don't have hair.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

CCC1 is essential for pH balance and normal cell function in plants.

BMP receptor IA is essential for proper hair cell differentiation in mice.

Mutation in hairless gene may increase hair loss risk.

Lnc056 helps hair follicle stem cells grow by increasing TRIP6 expression.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Certain genes help dermal papillae cells in hair follicles grow and group together.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Higher CRHR1 levels in AA patients lead to increased inflammation.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

ELIP-based CRISPR delivery improves heart disease gene editing but needs more testing.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Mutation in hairless gene may increase hair loss risk.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.