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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Overexpression of HDGF in melanocytes does not cause cancer.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Wool follicles are complex, involving interactions between different cell types and structures.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.

Endoxan often causes hair loss, which usually starts in the third week of treatment.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

PGF_2α receptors in human eyelids are found in specific parts of hair follicles, explaining eyelash changes with glaucoma treatment.

Hair is a complex organ, and understanding its detailed structure and growth phases is crucial for analyzing substances within it.

The document explains the genetic causes and characteristics of inherited hair disorders.

Dilated pupils can be an early sign of HIV/AIDS.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

The document concludes that understanding tissue degeneration is crucial for diagnosing skin lesions.

The study suggests a link between varicella-zoster virus and segmental vitiligo, with evidence of the virus disrupting skin pigment cells.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Root hair growth in plants is a complex process controlled by many factors working together.

Keratin proteins are crucial for hair growth and structure.

Keratin 26 affects cashmere goat hair growth and is influenced by various treatments.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.