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The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

Runx1 helps control the KAP5 gene in human hair follicles.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Removing SIX1 in fat cells reduces skin fibrosis.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

RIPK1 inhibitors might help prevent alopecia areata.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Mouse skin cancer progression involves a unique group of cells marked by ABCG2 and MTS24.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Raptor and Rictor have stable expression in hair cycles, with Raptor marking stem cells and Rictor involved in hair shaft formation.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Accurate diagnosis of RDEB-mitis in older adults is crucial for proper management without immunosuppressants.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

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

HPV8 E6 gene causes growth of certain skin stem cells.

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

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

The mystacial pad's innervation in adult rats is more complex than previously thought.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

Measuring minimal residual disease on day 15 helps identify high-risk leukemia patients.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Sunlight simulation causes skin inflammation, with different skin types reacting at different levels of exposure.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

RORA affects hair follicle stem cells' structure and movement, potentially helping treat hair loss.