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Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Researchers found a new mutation causing total hair loss from birth.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

HuR is essential for Treg function and preventing autoimmunity.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

A specific gene mutation causes sparse, brittle hair in a family.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Rac1 is crucial for normal hair structure and pigmentation.

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

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

BMP signaling helps prevent skin tumors by blocking cancer-promoting pathways.

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