Search

everythinglearnresearchcommunity

for

Search:↓

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

BST2 protein and certain T cells increase in early alopecia areata.

BTNL2 helps protect hair follicles from immune attacks.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The new collagen template speeds up production and supports skin healing without harmful reactions.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

TP0427736 may help treat hair loss by blocking a specific protein and promoting hair growth.

The scraggly mutation causes hair loss and skin defects in mice.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Ubiquitination of the insulin receptor regulates collagen secretion in human skin.

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

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

Graft-versus-host disease is a complication where donor immune cells attack the recipient's body, often affecting the skin, liver, and gastrointestinal tract.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

Dystonia may be part of PAS-4 and linked to immune issues.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.