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The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A rare scalp condition caused scarring hair loss in a woman, improved slightly with treatment.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

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

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

A new therapy for a skin blistering condition has not been developed yet.

Laser microdissection helps get DNA from single hair follicles for better forensic analysis.

Bleomycin injections in mice cause skin thickening and hair loss.

Fibroblast behavior is key for skin structure and healing.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A fungus is essential for forming and shaping hair ice on dead wood.

Cross-linked proteins help maintain the structure of hair, feathers, and hagfish teeth.

Curly wool has more orthocortex than straight wool.

A new method accurately measures molecular movement without complex modeling.

A dark-haired Chinese girl had hair that looked banded under certain light but was normal under a microscope.

Selective photothermolysis can target sebaceous glands and may treat acne effectively.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Lupus nephritis can cause severe kidney and blood vessel problems.

Fibroblast spheres can form stem cells, but marker distribution needs more study.

Localized dystrophic epidermolysis bullosa (DEB) can lead to scarring alopecia, highlighting the need to recognize and address this complication.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

Hair beds in fluid show nonlinear response due to viscosity, inertia, and elasticity.

Careful histologic examination is crucial to differentiate types of bullous lesions in cutaneous lupus erythematosus.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.