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ALRN-6924 may prevent hair loss caused by chemotherapy.

BTNL2 helps protect hair follicles from immune attacks.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

A new gene mutation causes insulin resistance in a girl and her mother.

OsPHR2 gene in rice enhances root growth and phosphorus accumulation.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

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

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

A woman's hair loss worsened after starting hepatitis C treatment due to immune changes in her hair follicles.

Enhancing Tregs can protect against alopecia areata.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A mutant FERONIA gene affects root hair growth at high temperatures.

pCLCA2 protein may help maintain skin structure and function.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

Farudodstat may effectively treat alopecia areata without harmful side effects.

Blocking IL-12 can help treat alopecia areata by preventing hair follicle immune issues.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

OR101 may effectively treat atopic dermatitis and similar skin conditions.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Peginterferon alpha-2a effectively treats acute hepatitis C in hemodialysed patients, despite some side effects.

3D-ultrasound can non-invasively detect and predict alopecia areata phases and outcomes.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.