Search

everythinglearnresearchcommunity

for

Search:↓

Iron supplements may reverse premature graying in iron-deficient individuals; ingrown nails are common in diabetics with certain risk factors; topical finasteride may reduce scalp DHT as effectively as oral finasteride; monilethrix treatment is challenging but some medications can help.

Iron supplements may reverse premature hair graying caused by iron deficiency.

Finasteride solution helps treat hair loss.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

AP collagen peptides improve hair elasticity and gloss.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Monilethrix causes different levels of hair loss in family members.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

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

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Monilethrix causes fragile, patchy hair loss.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

New genetic mutations linked to rare skin disorders were found in three newborns.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.