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Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

α-Phellandrene may help prevent hair loss by increasing growth factors and cell growth in hair cells through a specific signaling pathway.

Shampoo with heat-killed Lacticaseibacillus paracasei GMNL-653 improves scalp health and hair growth by changing scalp bacteria.

Genomic research can help improve the quality and production of natural fibers in animals.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Further research is needed to understand how the microbiome affects hair loss in Alopecia Areata.

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

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

PRP may help with aging and osteoarthritis, improving tissue repair and reducing surgery risk.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

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.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

Researchers found genes linked to hair loss in male giant pandas.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

Androgenetic alopecia involves immune cell disruptions, especially increased CD4+ T cells around hair follicles.

Fire Needle Therapy may help bring back skin color in vitiligo by affecting cell growth signals.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

UV exposure reduced hair shine in mice, but minoxidil helped restore it.

Honeybees face serious threats from various diseases, but beekeepers use several methods to manage and control them.

New findings may help diagnose and understand scarring alopecia better.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.