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L-cysteine slows down the breaking of bonds in hair due to electrostatic interactions.

NFIC helps rat dental cells grow and turn into bone-like cells.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

Cyclosporine A slowly changes cell membranes, explaining some of its effects and side effects.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Mutations in specific genes cause different types of ectodermal dysplasias.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Somatic BHD mutations are rare in Japanese renal tumors.

Cantú syndrome is caused by mutations in the ABCC9 gene.

TCDD reduces EGF receptor activity and causes various developmental changes in animals.

Mutating the gmds gene in zebrafish increases hair cell numbers and regeneration.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Two distinct caspases in human skin help with cell death and skin formation.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

Mice without Vitamin D receptors have hair growth problems because of issues in the hedgehog signaling pathway.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Human mitochondrial DNA polymerase makes very few errors, crucial for preventing degenerative diseases.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Vitamin D3 and its receptor help protect skin from UVB-related cancer.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.