Search

everythinglearnresearchcommunity

for

Search:↓

Proteins influence the quality and traits of cashmere goat fleece, affecting hair strength and diameter.

Children with different rheumatologic diseases have specific skin symptoms that can help with diagnosis.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

Lichen planopilaris and frontal fibrosing alopecia are likely the same disease with different clinical appearances.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

A woman was injured by a hedgehog falling on her, causing skin lesions but no disease.

Accurate diagnosis of cicatricial alopecias requires thorough scalp examination and multiple biopsy techniques.

The document suggests a possible connection between rapid weight loss and hair loss, and reports a case of skin condition improvement after stopping acne medication.

EGFR is essential for normal hair development and follicle differentiation.

Hair treatments and dehydration affect hair's lipid and protein behavior, influencing its flexibility and appearance.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Analyzing trace elements in human hair is complex and needs a standardized method.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

The new 3D bioprinting method successfully regenerated hair follicles and shows promise for treating hair loss.

The book was the first to focus on the biophysical properties of hair.

Defects in certain proteins cause major heart abnormalities during early development.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Two new types of eyelid cysts were identified, each with different treatment challenges.

Human hair's structure and properties were studied using advanced microscopes and mechanical tests.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

Hair patterns in mice are controlled by both a global system dependent on Fz6 and a local self-organizing system.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.