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Optimizing the structure of a specific compound greatly improved its effectiveness and precision for treating diabetic complications.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

The document concludes that the skin is a complex organ providing protection, sensation, and healing, with challenges in treating conditions like itchiness.

The conclusion is that tissue structure is key for stem cell communication and maintaining healthy tissues.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Scientists created early-stage hairs from mouse cells that grew into normal, pigmented hair when implanted into other mice.

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Hormones and genes affect hair growth and male baldness.

Hair and wool strength is affected by the number and type of bonds in their protein structures, with hair having more protein aggregates than wool.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Surface-modified nanostructured lipid carriers can improve hair growth treatments.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Androgenic alopecia causes hair follicle degradation and skin restructuring, but some hair elements remain.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

New treatments for skin and hair repair show promise, but further improvements are needed.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

People with alopecia areata have similar retinal structures but thicker choroidal regions compared to those without the condition.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Scientists have developed a method to keep chicken feather follicles alive and structurally intact in a lab for up to a week.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Adult skin cell-based early-stage skin substitutes improve wound healing and hair growth in mice.