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Certain natural and synthetic compounds may help treat inflammatory skin diseases by targeting a specific signaling pathway.

Understanding keratinization is crucial for treating skin conditions like ichthyoses and psoriasis.

A specific gene mutation causes congenital hair loss.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

Anticonvulsant drugs may cause temporary chromosomal abnormalities.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Hair loss can be linked to hormonal changes, and physical conditions like heart defects can cause depression.

Gomez–Lopez–Hernandez syndrome can cause focal hair loss and developmental delays but some children can still function well and excel in school and sports.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Chromosomal changes, including those in the WRN gene and rDNA, may significantly contribute to aging.

New genes and pathways are important for testosterone production and male sexual development.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Male and female bodies respond differently to stress, influenced by hormones and development stages, with implications for stress-related diseases.

Thymosin β4 helps improve skin healing and reduce scarring.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Dihydrotestosterone treatment on 2D and 3D-cultured skin cells slows down hair growth by affecting certain genes and could be a potential target for hair loss treatment.