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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

FGF13 gene changes cause excessive hair growth in a rare condition.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The new delivery system improved raloxifene's skin absorption and effectiveness against cancer cells.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

A gene mutation in mice causes permanent hair loss and skin issues.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

A specific RNA molecule blocks hair growth by affecting a protein related to hair loss conditions.

New LSS gene variants help understand congenital hypotrichosis 14 better.

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

PNU 157706 is a more effective treatment than finasteride for conditions caused by DHT, like enlarged prostate and hair loss.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

PDGFC gene may help select goats with desirable curly wool traits.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Certain IL-18 gene variations may increase the risk of alopecia areata.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Cutaneous gene therapy could become a viable treatment for skin and hair disorders with improved vector development and gene expression control.

Phospholipase A2 is necessary for the correct placement of PIN proteins in plant roots, affecting root growth.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.