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FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

The protein's size was reduced, but more work is needed to confirm its function.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The LEF-1 binding site enhances gene expression in hair follicles, with other proteins aiding specific regulation.

The patient responded well to treatment with no disease progression.

Plet-1 protein helps hair follicle cells move and stick to tissues.

RAGE is a potential target for melanoma treatment, but its effectiveness is uncertain due to variable expression levels.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

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

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Targeting the TNFRSF1B gene may help treat hair loss.

Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

UC.145 may be a new biomarker for predicting gastric cancer.

LMWP-PDGFA shows promise for improving hair health and treating hair loss with fewer side effects.