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Tofacitinib effectively improved hair regrowth and skin condition in a woman with alopecia totalis and lichen planus hypertrophicus.

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

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Overexpressing 14-3-3σ in mice skin reduces cell growth and hair density.

miR-199a-3p controls hair growth and is linked to alopecia areata.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Blocking mTORC1 activity could increase hair pigmentation and potentially reverse greying.

Sacituzumab tirumotecan shows promise in treating breast cancer with manageable side effects.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Mitochondriopathy may cause eyelash loss.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Increasing m6A levels can improve skin cell growth and wound healing.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

New mutations in the hairless gene may cause hair loss and affect bone development.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Overexpression of the HE4 gene in mice causes eye inflammation and cloudiness.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A mutation in the human hairless gene causes alopecia universalis.

Collagen XVIII and Bmx tyrosine kinase are important for hair growth and skin cancer development.