Search

everythinglearnresearchcommunity

for

Search:↓

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Certain gene variations increase the risk of alopecia areata in Koreans.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

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

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Compound 7b is a promising candidate for treating benign prostatic hyperplasia and prostate cancer.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

Hair sensitivity to androgens is partly controlled by specific enzyme expressions in different hair areas.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

A genetic variant in the KRT25 gene causes tightly curled hair.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

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

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.