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The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Certain gene variations are linked to the thickness of cashmere goat hair.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Intestinal stem cells can help repair skin damage from radiation.

Adrenal disorders can cause lasting brain and behavior issues in children.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

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

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Hormone treatments in transsexual individuals reduce hair growth and oil production in male-to-females and increase them in female-to-males.

Aromatase gene variation may increase female hair loss risk.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.