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A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

SOX4 is crucial for the development of melanoma.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

Mutations in the HOXC13 gene cause hair and nail development issues.

The Paxbp1 gene is crucial for healthy hair follicles.

Deleting part of a gene in mice causes wavy hair and high pup loss.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

FGF18 may influence hair loss in dogs.

Finasteride reduces AML cell growth by inhibiting androgen receptors.

Editing the FGF5 gene in sheep increases wool length, confirming its role in hair growth.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

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

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

HuR is essential for Treg function and preventing autoimmunity.

The agouti gene may help understand and treat obesity.

ZmSPL10, ZmSPL14, and ZmSPL26 genes are essential for forming maize structures needed for pollen capture and kernel production.

Folliculin slows hair growth, and blocking it might help treat hair loss.

Recombinant Human Annexin A5 may help treat localized scleroderma by reducing skin thickening and inflammation.

Follistatin helps hair growth and cycling, while activin prevents it.

Frontal fibrosing alopecia is a challenging hair loss condition with no known cause or definitive treatment.

Male mice with FGF5 mutations grow longer hair than females.

Msx2 deficiency in mice leads to bone growth and organ development problems.

Lack of Fgf21 slows hair growth by affecting gene interactions.