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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

New treatments may restore cancer-blocking proteins, slow prostate cancer, identify drug targets, and potentially regrow hair.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

ACTH-dependent Cushing's syndrome linked to metastatic cervical cancer is rare and has high risks.

A woman with a rare hair loss condition developed skin cancer in the bald area.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

VCAM1 appears early in kidney injury and signals future nephron loss.

Paclitaxel and nab-paclitaxel can be safe and effective for advanced gastric cancer patients on hemodialysis.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Cyclophosphamide is preferred for severe cases in pediatric rheumatology and nephrology despite its side effects.

Cyclosporine can reverse hair graying.

Enhancing CD8+ T cell function to induce ferroptosis in tumor cells may help treat skin melanoma.

Keratoacanthomas and squamous cell carcinomas have similar keratin patterns, making them hard to tell apart.

A rare nail bed cancer was successfully treated with no recurrence after 4 years.

PHGDH promotes cancer growth by aiding cell proliferation and tumor progression.

A kidney transplant patient developed leprosy, likely due to immunosuppression and genetic factors, and improved with treatment.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Researchers developed promising agents for prostate cancer imaging, with the best one showing high potential for clinical use.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Recent findings advanced understanding of cancer mechanisms and potential treatments.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

A rare tumor caused unusual hormone production leading to Cushing syndrome.

Inherited color dilution in rabbits is linked to DNA methylation changes.

The patient had complex urinary tract issues and ambiguous genitalia, with physical features suggesting a hormonal imbalance.