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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Thymic stromal lymphopoietin (TSLP) promotes hair growth by stimulating specific skin cells.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Certain gene variants may raise the risk of prostate enlargement, but taking NSAIDs could reduce this risk.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

FOXN1 gene variants cause low T cells and immune issues from birth.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

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

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A genetic variant linked to hair thinning in Japanese women was found.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.