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Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

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.

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

Most ingredients in anti-hair loss products lack scientific proof of effectiveness.

Exosomes from human fat stem cells can potentially enhance hair growth and survival, providing a new possible treatment for hair loss.

Home-use cosmetic laser and light devices show modest results for hair removal and acne treatment, but more research is needed for confirmation.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

Rice derivatives in conditioners protect and improve hair health.

Mutations in the AR gene cause hair thinning and loss.

Applying a special DNA plasmid to the skin can make it thicker and stronger.

A new gene mutation causes long hair in some Maine Coon cats.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

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

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

BMAL1 and Period1 genes can influence human hair growth.

Oral zinc sulphate is an effective and safe treatment for thallium poisoning.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Alopecia areata causes varying hair loss patterns, affecting hair, nails, and possibly glands, with treatment outcomes depending on disease duration and extent.

The document concludes that better biomarkers are needed to detect long-term oral testosterone use in athletes.

The hair follicle bulge is an important area for adult stem cells involved in hair growth and repair, with potential for medical use needing more research.

Special particles from umbilical cord stem cells help heal skin wounds in diabetic mice by preventing certain immune cell death.

The document explains the genetic causes and characteristics of inherited hair disorders.

5α-reductase inhibitors can interfere with doping tests by masking banned substances.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The document concludes that alopecia has significant social and psychological effects, leading to a market for hair loss treatments.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Nutrients like vitamins, copper, zinc, and amino acids are crucial for healthy hair and wool growth.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.