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Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

PI3Kδ inhibition may effectively treat cutaneous chronic graft-versus-host disease.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Sox13 is a new marker for early hair follicle development and differentiation.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

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.