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

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

New mutations in the hairless gene may cause hair loss and affect bone development.

Rat dermal papilla cells have unique genes crucial for hair growth.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

HB24 helps convert IBA to IAA, promoting root hair growth.

Retinoic acid and DMSO improve gene delivery to mouse skin for potential hair and skin disease treatment.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

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

Overexpressing AVP1 and AtNHX1 in plants improves salt tolerance and root hair development.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

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

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

LED light helps human hair root cells grow and move by activating certain cell pathways.

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.

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

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Restoring EDA and WNT pathways early may help improve skin, hair, and teeth issues in hypohidrotic ectodermal dysplasia.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Dkk4 protein is necessary for the proper development and arrangement of hair follicles.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Rat hair-follicle stem cells can become heart cells with specific supplements.