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The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

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

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

High doses of Lepidium sativum seed extract are toxic and should be used with caution.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Machine learning is effective in predicting gene functions and their relationships with diseases.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

The FAW-FS algorithm improves depression recognition, and psychological interventions help AGA patients' mental health.

The combination of hair follicle stem cells and PRP shows promise for treating hair loss in Asian men and women.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Cantú syndrome is caused by mutations in the ABCC9 gene.

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

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

COVID-19 may harm male fertility and damage the reproductive system.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

Hair protein analysis might help identify a person's ethnicity, sex, and age in forensics.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.