Search

everythinglearnresearchcommunity

for

Search:↓

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

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

Gender affects hair and scalp characteristics, with differences in hormone responses, graying patterns, and trace metals.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Arctiin helps protect hair cells from damage and death caused by oxidative stress.

Sex and sex hormones can affect brain inflammation in Parkinson's disease, with male mice being more affected and female mice showing a protective effect.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

A girl inherited excessive body hair from her mother and grandmother.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

New treatments for alopecia areata may target specific immune cells and pathways involved in hair loss.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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

Two mouse mutations cause similar hair loss despite different skin changes.

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.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.