Search

everythinglearnresearchcommunity

for

Search:↓

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Exosomes can be used for diagnosing and treating skin conditions and improving skin health.

Sox13 is a useful marker for early hair follicle development but not essential for hair growth.

DNA phenotyping can predict physical traits like eye, hair, and skin color, improving forensic investigations.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

Ptprq has multiple forms that change during inner ear development.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

Ixekizumab is effective and safe for patients who did not improve with etanercept treatment for psoriasis.

Different PADI isoforms help cells develop diverse functions.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

CXCR2 in skin cells promotes tumor growth.

A gene mutation in mice causes skin defects and early death.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Bexxar is highly effective as a first treatment for non-Hodgkin's lymphoma, with most patients alive and many in remission after eight years.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Oncology specialists are disappointed by the discontinuation of the effective lymphoma treatment Bexxar.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Researchers found 15 new genetic links to skin traits in Japanese women.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The exosome injections were from stem cells and plants, not umbilical cords.

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