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Higher granulysin levels in the blood are linked to more severe hair loss in alopecia areata patients, and these levels decrease after effective treatment.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Early identification of lupus through skin signs and blood tests is crucial in India.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

Both genetic and lifestyle factors significantly affect female hair loss.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

A gene mutation causes woolly hair in a Syrian patient.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

AGA is a genetic, hormonal hair loss treated with finasteride, minoxidil, and supplements, but new compounds are being developed.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

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

The document explains the genetic causes and characteristics of inherited hair disorders.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Measuring reproductive hormones in brown bear hair could help identify their sex and reproductive state, but better collection methods or lab techniques are needed.

Women under 55 with hair loss (AGA) may have a higher risk of heart disease (CAD).

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

High testosterone to epitestosterone ratio in hair could predict male-pattern baldness.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

PAON shows skin patterns due to genetic mosaicism.

Trichoscopy helps diagnose hair and scalp problems but isn't always definitive and should be used with other methods.

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

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.