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Low testosterone in men is a risk factor for a specific heart rhythm issue, and testosterone treatment may help prevent it.

Low testosterone can cause a heart rhythm problem in men, but fixing it can prevent the issue.

Trichorrhexis invaginata can occur with tinea capitis, though it's rare.

Sporadic trichoblastic neoplasms generally don't recur or spread, with one case showing a specific genetic fusion.

RTA 408 cream protects mice from radiation skin damage.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

TTD symptoms vary widely, requiring thorough evaluations.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

Thyroid hormone receptor β1 is found in human hair follicles and helps them survive.

Trichotillomania was successfully treated with risperidone and naltrexone.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

Injecting recipient splenocytes into donors' thymus can prevent graft-versus-host disease.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Patients with thyroid disorders show different symptoms and antibody levels.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

A brain injury can lead to compulsive hair-pulling and psychosis-like symptoms, needing comprehensive treatment.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Hair transplant surgery effectively treated a specific type of hair loss and is recommended as a primary treatment option.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Trichotillomania may have a genetic link to psychiatric disorders.

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

Localized trichorrhexis nodosa is a hair condition where hair becomes fragile and breaks easily due to damage.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.