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Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

FGF13 gene changes cause excessive hair growth in a rare condition.

Non-coding RNAs could help detect and treat radiation damage.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Stem cell therapies show promise for hair regrowth in androgenetic alopecia.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Mouse Notch is important for determining cell roles in hair follicles.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Genetic differences between young and old Tan sheep explain why their fleece changes from curly to straight as they age.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Topical immunotherapy is the best treatment for severe alopecia areata.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

EGFR helps control how hair grows and forms without needing p53 protein.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

The KRTAP21-2 gene affects wool length and quality in sheep.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

Tradescantia plants can effectively test for the toxicity of harmful algae.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

The 595-nm pulsed dye laser effectively reduces symptoms of EFFC with minimal side effects.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The document's conclusion cannot be provided because the document is not accessible or understandable.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

DHT in the human prostate is produced through multiple pathways, not just from testosterone.

Cantú syndrome is caused by mutations in the ABCC9 gene.