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Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

Hair in mammals likely evolved from glandular structures, not scales.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

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

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

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

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

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

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Certain cells from hair follicles can create new hair and contribute to hair growth when implanted in mice.