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Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Hair loss gene found on chromosome 3q26.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Trichotillomania may have a genetic link to psychiatric disorders.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

High proliferation and cell delamination drive early skin development, while later stages may not rely on cell division orientation.

Specialized ribosomes affect aging in human skin cells.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Histone demethylases can change gene expression and may be linked to diseases like cancer.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Monilethrix is a genetic disorder causing brittle hair, diagnosed using tricoscopy.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

CTCF protein is essential for skin and hair follicle development in mice.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.