Search

everythinglearnresearchcommunity

for

Search:↓

Childhood and adult height, and early immune-related hospitalizations increase testicular cancer risk, while baldness, larger families, and sports reduce it.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Tanshinone IIA helps protect skin tissue from low oxygen damage by boosting certain cell markers.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Scientists made a mouse that can be made to lose hair and then grow it back.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

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

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

Inhibiting TYK2 can restore hair growth in alopecia areata.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

Trichilemmal carcinoma shares genetic traits with other skin cancers, suggesting similar treatment options.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Two new gene mutations cause a rare hair disorder.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

Gene variations may increase oxidative stress in male pattern baldness.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

Two siblings have a rare hair condition caused by a new genetic variant.

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.