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Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Egfl6 is not needed for zebrafish face development.

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

A new keratin gene was found in mice, explaining hair growth.

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.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

A gene mutation in Lama3 is linked to a common type of hair loss.

LHX2 is crucial for development, tissue repair, and preventing diseases.

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

Zfp157 is active in many mouse tissues during development and in specific adult cells.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

CDP is crucial for lung and hair follicle cell development.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

miR‑339‑5p can slow down hair follicle stem cell differentiation by targeting DLX5.

Hex gene plays a crucial role in starting feather development in chick embryos.

Mouse keratin 6 genes evolved independently from human ones and are regulated differently.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Overexpression of LRIG3 in skin causes hair loss.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Lhx2 is essential for effective Sonic Hedgehog signaling in early retinal development.