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

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

Non-surgical procedures can help reduce wrinkles and stimulate skin repair by understanding skin aging at the molecular level.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Skin cancer in sun-exposed areas is more likely to come back.

Genes linked to wool fineness in sheep have been identified.

Iron deficiency is the main cause of hair loss in women, and iron supplements started within 6 months can improve hair health.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Dihydrotestosterone causes p27 protein breakdown in ovarian and breast cancer cells by binding with SKP2.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.