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Men with early hair loss may have a higher risk of enlarged prostate and possibly prostate cancer due to shared hormonal factors.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A protein found in safflower seeds can stimulate hair growth and speed up wound healing in mice.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Hair loss in men is mainly caused by hormones and genes, and while current treatments can slow it down, they can't fully stop it.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Betamethasone dipropionate reduced skin thickness, fish oil increased it, and combined treatment had no significant effect.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Hypothyroidism may cause certain types of hair loss.

Minoxidil and finasteride are effective for treating hair loss, with dutasteride showing potential but with side effects.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

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

Ectodysplasin signaling is crucial for skin appendage development, requiring specific doses and durations.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Genetic factors and diet significantly increase the risk of male pattern baldness.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Dutasteride is more efficient than finasteride, but individual results vary.

Alopecia areata, a type of hair loss, may be passed through T cells and has genetic links, while treatments vary in effectiveness. Male pattern baldness can be treated with finasteride and is influenced by androgens in hair follicles.

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