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

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Different enzymes are active in different parts of developing mouse organs.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

15-lipoxygenase helps keep skin healthy by reducing inflammation.

Reducing FOXA2 in skin cells lowers their ability to grow hair.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

lncRNAs play a key role in hair follicle development, affecting cashmere quality and yield.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

Id2 gene helps keep hair follicle stem cells inactive.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

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

Four new genes related to sheep wool were discovered, showing genetic diversity.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

Retinoic acid affects skin and hair health by working with specific receptors, and its absence can lead to hair loss and skin changes.

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

Elf5 is important for skin stem cell growth and could help treat skin and hair problems.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

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 gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.