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MCHR2 gene duplications may be linked to alopecia areata.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Hydroxypinacolone retinoate is a potent anti-aging ingredient for skin that is more effective and less irritating than other forms of retinoids.

A gene variant causes a skin and hair disorder by disrupting protein balance.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

ESR2 gene linked to female-pattern hair loss.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Dutasteride effectively treats benign prostatic hyperplasia and may reduce prostate cancer risk.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

UHP-sCESr is as effective as HESr for treating BPH symptoms.

HPV16-transformed cells can change human skin cell properties, aiding tumor growth.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

The patient with a misplaced pituitary gland and interrupted pituitary stalk is being treated with hormone replacement.

Low androgen levels can still cause female pattern hair loss.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A mutation in the human hairless gene causes alopecia universalis.