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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

ESR2 gene linked to female-pattern hair loss.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Fgfr2b helps maintain healthy skin and prevent cancer.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

MOF controls skin development by regulating genes for mitochondria and cilia.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Type II keratin genes are crucial for hair follicle differentiation and have a conserved structure and expression pattern.

LHX2 is essential for hair follicle development, controlled by NF-κB and TGFβ2 signaling.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Only two of the four keratin genes are expressed in wool fibers.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

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.

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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A gene mutation causes monilethrix in a Chinese family.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Transfected cells with VEGF and FGF2 genes improve skin wound healing by enhancing blood flow and regeneration.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.