Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Higher nitric oxide synthase levels in the scalp may influence hair loss in androgenetic alopecia.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Higher Claudin 3 levels in the blood are linked to more severe alopecia areata.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Elevated granulysin levels may indicate disease activity in vitiligo and alopecia areata.

AMN can cause bladder problems due to nerve damage.

Peanut agglutinin staining helps differentiate malignant melanoma from nevocellular nevus.

Increased LC3 gene expression may be linked to premature graying of hair.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Two specific genetic markers increase the risk of hair loss in Asian populations.

ATP6AP1‐CDG can cause hearing loss, hair loss, and protein issues, even in female carriers.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

New mutations in the DSG4 gene cause a rare hair condition.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

5α-reductase affects dopamine receptors linked to sensorimotor gating, which may help understand disorders like schizophrenia.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.