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Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

TSC2-/meth cells can cause skin lesions, hair growth, and lung issues, and may be treated with chromatin remodeling agents.

The same gene mutation can cause different symptoms in family members.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Scientists found new, better-working inhibitors for a hormone-related enzyme.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Fatp4 is crucial for healthy skin development and function.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

Controlling Tslp can improve health in AEC syndrome patients.

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

Hair loss in certain mice is linked to changes in keratin-related genes.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

Two siblings have a rare hair condition caused by a new genetic variant.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Minoxidil helps restore thymus size in 22q11.2 deletion syndrome.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

Rhizobacterial strain RT3 helps lettuce survive drought by producing protective substances like proline.

Sulfated polysaccharides from Microcosmus exasperatus may help treat cancer without causing blood thinning.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.