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Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Finasteride blocks progesterone's effect on absence seizures in rats.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

Oral minoxidil is more convenient but topical minoxidil improves hair density better.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

Platelet-rich plasma may improve hair density in androgenetic alopecia patients.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Cross-section trichometry is an accurate method to measure hair loss and growth.

Hair loss in men treated best with early medication or transplant, new treatments researched.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

The visfatin GT genotype may increase the risk of Alopecia Areata.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Scientists found a gene in mice that causes early hearing loss.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

The hypothesis suggests that PCOS may start early in life due to genetic and environmental factors, influencing future reproductive and metabolic problems.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

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.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Finasteride can cause skin rash.

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

A 7-month-old girl with a rare skin disorder died because diagnosis was delayed.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Men are more likely to have severe COVID-19 cases and fatalities than women due to factors like lifestyle, aging, and biological differences.