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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The HCR gene contributes to psoriasis risk.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Non-coding RNAs play key roles in the hair growth cycle of Angora rabbits.

Boys with less severe EDA mutations in XLHED have milder symptoms and better sweat and hair production.

Skin and hair can help us understand organ regeneration, especially how certain stem cells might be used to form new organs.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Stem cells can help other stem cells by producing supportive factors.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

Nitroxide drugs can safely and effectively treat age-related diseases like macular degeneration and cardiovascular issues.

Scientists have made progress in growing mini-organs and regenerating parts of the skin, with plans to treat hair loss in a future trial.

The model accurately predicts age from saliva and buccal cells for forensic use.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

New genes linked to woolly hair have been found, which could help treat it and change hair texture.

Genetically variant peptides are reliable for forensic identification despite age-related changes in hair proteins.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Haplogroup X found in Altaian population supports Amerindian origin.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

H19 boosts hair growth potential by activating Wnt signaling, possibly helping treat hair loss.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

Organs like hair follicles can renew themselves in complex ways, adapting to different needs and environments.

Early diagnosis and treatment of biotinidase deficiency are crucial to prevent vision problems.