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Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Minoxidil improved hair growth in a child with a rare genetic disorder.

A new gene variant causes glucocorticoid resistance in a mother and son.

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

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

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

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Understanding genetics is crucial for treating heart and skin diseases.

Hair loss in men treated best with early medication or transplant, new treatments researched.

EGFR-TKIs can cause significant skin, nail, and organ side effects.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The rise in tinea capitis cases in Stockholm is linked to increased African immigration.

Fingerprints form uniquely before birth due to specific genetic pathways and local signals.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Regulating certain sex hormones may help delay facial aging.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Certain genes are linked to the risk of developing Alopecia Areata.

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

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