Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Activating cannabinoid receptor 1 may help manage psoriasis by reducing certain keratins.

RANKL helps regenerate lung cells, potentially aiding lung repair in diseases like COPD.

HOXC13 is essential for hair and nail development by regulating Foxn1.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Glucocorticoids reduce fat production in liver cells, while androgens increase it in females; manipulating certain enzymes can influence these effects.

Atg5 can promote tumors when autophagy is deficient but suppresses them under normal conditions.

AHR ligands could treat inflammatory skin diseases.

Gene variation affects prostate issues and hair loss.

Neuroactive steroids affect cocaine's rewarding effects through the sigma1 receptor.

Poly(ADP-ribose) synthesis is linked to skin cell differentiation.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

5α-reductase deficiency can cause ambiguous genitalia and gender dysphoria, treatable with testosterone.

A rare genetic condition can mimic symptoms of other diseases, making diagnosis challenging.

17β-estradiol can reduce inflammation in the skin.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Recombinant Human Annexin A5 may help treat localized scleroderma by reducing skin thickening and inflammation.

Rizatriptan benzoate-loaded dissolving microneedles are effective and convenient for treating acute migraines.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Mice with the naked gene have missing or abnormal hair cells.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

Male cells need DHT to respond to testosterone, while female cells do not.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

ELF5 is essential for skin cell growth and maintenance.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

BTNL2 helps protect hair follicles from immune attacks.