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African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

Researchers found four genes that could help diagnose severe alopecia areata early.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Early diagnosis and personalized treatment for PCOS are crucial, especially for young women in West Bengal, India.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Vitamin D receptor gene variations are not linked to alopecia areata.

SLCO genes may predict prostate cancer mortality risk, and lifestyle changes improve health in advanced prostate cancer.

CAG repeat length in the AR gene is not linked to PCOS risk in Iranian women.

People with celiac disease have a higher risk of developing alopecia areata.

People with atopic dermatitis have a higher risk of developing keloids, especially women, those under 40, and those with severe symptoms.

Hereditary factors affect acne duration, not severity, and late-onset acne in females has different causes.

Found new possible treatments for hair loss.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.

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

Male pattern baldness is partly caused by specific genes, but most genetic factors are still unknown.

No link found between new male baldness genes and female hair loss.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

A boy's hair turned red because of genetic mutations, not lack of zinc.

A new gene mutation causes a rare type of hair loss.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

The study concluded that genetic mutations affect human hair diseases and identified key genes and pathways involved in hair growth and cycling.

Gene differences affect finasteride side effects in men with hair loss.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Male and female hair loss have different genetic causes.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

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

Arab APS1 patients have unique and recurrent AIRE gene mutations.