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The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Diphenylcyclopropenone is more effective and has fewer side effects than dinitrochlorobenzene for treating alopecia areata.

Early detection of apolipoprotein levels helps reduce depression risk in the elderly.

DP cells interact with immune cells, possibly causing hair loss in Alopecia Areata.

C4BPA protein may link acne severity and insulin resistance.

CCC1 is essential for pH balance and normal cell function in plants.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

CD1d expression in scalp skin and hair follicles changes with the hair cycle and may help protect against microbes.

The clinical signs of Adams-Oliver syndrome can vary greatly, even among family members.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

FAPD in children may not depend on androgens and should be treated with anti-inflammatory measures and minoxidil.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Agouti and AGRP affect pigmentation and obesity, with implications for metabolic disorders.

The TPAP method effectively categorizes androgenetic alopecia patients with high accuracy, but needs real-world validation.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

KRTAP28-1 gene can help breed sheep with finer wool.

PPARγ signaling modulation can protect hair follicle stem cells from chemotherapy-induced damage.

The man's hair loss and skin papules were diagnosed as atrichia with papular lesions, not alopecia areata universalis.

New mutations in the hairless gene may cause hair loss and affect bone development.

A man developed severe skin reactions after using a treatment for hair loss.

Upadacitinib effectively treated a patient with multiple inflammatory conditions.

Timely diagnosis and treatment of complex autoimmune diseases like APS2 are crucial to prevent complications and improve life quality.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Potential therapeutic targets for scarring hair loss are identified.

A new treatment using unactivated platelet leukocyte autoplasma cured 80% of non-scarring alopecia patients.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

C-reactive protein helps monocytes stick to blood vessel cells by causing oxidative stress.