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The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Male androgenetic alopecia involves hair follicle miniaturization due to DHT, with potential treatments using inhibitors and blockers.

A young man was diagnosed with trichoepitheliomas, causing thick skin and hair loss.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Steatocystoma multiplex causes recurring skin cysts and needs early recognition for better management.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

The research found specific genes and proteins that affect how fast chickens' feathers grow, which is not solely determined by traditional inheritance patterns.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

The document concludes that various skin conditions have specific treatments, ranging from antihistamines for urticaria to surgery and medication for tumors and chronic skin diseases.

New treatments targeting specific genes show promise for treating keratin disorders.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Male pattern hair loss is genetic and influenced by hormones, with treatments like minoxidil and surgery available.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.