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Studying rare genetic disorders can help us understand and treat common diseases better.

Four genes are potential markers for hair loss condition alopecia areata, linked to a specific type of cell death.

A protein called HIF-1a helps control hair growth genes and could be targeted to treat hair loss.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

The document concludes that targeting 5α-reductase, the androgen receptor, and hair growth genes, along with using compounds with anti-androgenic properties, could lead to more effective hair loss treatments.

650 nm red light helps hair grow and prevents hair loss by affecting certain genes and biological processes.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

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

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

Alopecia areata is a common autoimmune disease affecting about 2% of people, causing significant disability and often associated with mental health issues and other autoimmune conditions.

Finasteride may help treat childhood brain tumors by activating certain genes.

CO2 laser treatment for aging skin significantly changes immune system-related genes.

Increased PPARGC1α relates to hair thinning in common baldness.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

AGA, a common hair loss, is caused by genetics, hormones, age, and environmental factors.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

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

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Cepharanthine helps reduce cell aging caused by the cancer drug Doxorubicin by boosting cell cleanup processes.

Sex hormones may be linked to inflammation in Hidradenitis Suppurativa.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.