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Minoxidil decreases LH expression, while hydralazine has mixed effects on prolyl and lysyl hydroxylase activities.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

The CRH/CRH-R1 system might be involved in causing lichen planus.

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

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

lncRNAs may regulate hair follicle development in Hu sheep.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Certain long non-coding RNAs are important for the growth of hair follicles in Inner Mongolian cashmere goats.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Specific keratin gene mutations can cause monilethrix.

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

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

MCHR2 gene duplications may be linked to alopecia areata.

Scientists discovered two versions of a new human hair keratin gene.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

A gene called HDAC9 might be a new factor in male-pattern baldness.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

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 Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.