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Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Skin aging is caused by stem cell damage and can potentially be delayed with treatments like antioxidants and stem cell therapy.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

The document concludes that various skin conditions have specific treatments, ranging from antihistamines for urticaria to surgery and medication for tumors and chronic skin diseases.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

The document describes skin diseases affecting the outer ear in dogs and cats, their spread to other body parts, and treatment options.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

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

5-alpha reductase deficiency leads to male sexual development issues and treatments like finasteride help with prostate enlargement and hair loss.

A new mutation in the HR gene causes hair loss in a specific family.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

PCOS is a complex disorder in women that can lead to various health risks and requires personalized treatment.

The document concludes that proper diagnosis and combined treatments are key for hirsutism management, and weight loss may help overweight patients.

Alopecia Areata is an unpredictable autoimmune hair loss condition with limited and variable treatment effectiveness.

The document concludes that early diagnosis and treatment of PCOS in teenagers is important for managing symptoms and preventing long-term health problems.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

Young women with nonclassic congenital adrenal hyperplasia may experience worse sexual function and mild depression compared to healthy women.