Search

everythinglearnresearchcommunity

for

Search:↓

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Gene regulation could revolutionize hair color by altering pigmentation from within.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Minoxidil, finasteride, and low-level laser light therapy are effective FDA-approved treatments for hair loss.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Hair diameter and curvature are mostly determined by genetics.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

The review concludes that more research is needed to better improve the health outcomes for people with Polycystic Ovarian Syndrome.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Twins had rare skin cysts likely due to genetics.

Improving knowledge and practices in animal fibre production is crucial to meet market demands and potentially revive natural fibres.

Oxidative stress may contribute to hair loss in alopecia areata and antioxidants could potentially help as a treatment.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.