Search

everythinglearnresearchcommunity

for

Search:↓

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.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Understanding how Regulatory T Cells work could help create treatments for certain skin diseases and cancers.

Early balding in young Indian men may indicate a higher risk of metabolic syndrome and potential heart disease.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

The over-the-counter supplement DHEA could make COVID-19 worse, especially in diabetics and people with G6PD deficiency.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Alopecia areata causes sudden hair loss, has genetic links, and can be managed but not cured.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Identified genes linked to male-pattern baldness may help develop new treatments.

Aromatase gene variation may increase female hair loss risk.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

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

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Permanent hair loss from cicatricial alopecia is treated by reducing inflammation and managing symptoms, but regrowth in scarred areas is unlikely.

Taking vitamin D might improve life for MS patients and reduce skin side effects from alemtuzumab treatment.

Androgenetic alopecia in men is genetic and linked to health issues like obesity and heart disease, with treatments including minoxidil, finasteride, and hair transplants.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Afro-textured hair needs personalized care due to its unique genetic traits.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.