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Anti-TNF-α therapy may increase the risk of developing alopecia areata, especially in those with a history of autoimmune disease.

New genetic mutations causing hair loss were found in a Chinese family.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

New genes linked to male pattern baldness were found on chromosome 20p11.

TRM21 helps control flavonoid production and root hair growth in Arabidopsis thaliana.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Certain HLA class II alleles increase or decrease the risk of alopecia areata.

A specific gene variation in goats is linked to better growth traits.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Björnstad syndrome causes twisted hair from birth.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

NFIC helps rat dental cells grow and turn into bone-like cells.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.