Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Deleting the Sox21 gene changes hair lipid composition and increases cholesterol sulfate levels.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

The HCR gene contributes to psoriasis risk.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The B2 genes are crucial for hair growth in rats.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

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

KRT72 gene helps form hair.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

The B2C promoter works in sheep cells but not in mouse embryos.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.