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The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

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

Tiny particles from skin cells can help activate hair growth.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

New treatments for skin and hair repair show promise, but further improvements are needed.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Wnt1a-conditioned medium from stem cells helps activate cells important for hair growth and can promote hair regrowth.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

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

Hair loss patients have different microbes in hair follicles, possibly affecting hair loss.

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

New technologies help us better understand how skin microbes affect skin diseases.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

People with alopecia areata have higher levels of RBP4 protein and antibodies against it.

Ficus carica extract improved fertility in rats and may help with certain health conditions.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Terbinafine and itraconazole are more effective against Microsporum canis than fluconazole and griseofulvin.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

Different types of skin on mice have unique chemical profiles related to how they grow and react to stress.

Botryococcus terribilis Ethanol Extract may reduce inflammation by changing gene expression in cells.

The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Curcumin may improve blood sugar levels and cholesterol in people with PCOS, but more research is needed.