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TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

TCDD reduces EGF receptor activity and causes various developmental changes in animals.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

Toluene diisocyanate exposure can cause immune sensitization by interacting with proteins in hair follicles and sebaceous glands.

Telocytes have potential in therapy and tissue regeneration, but challenges in identification and cultivation remain.

TTD symptoms vary widely, requiring thorough evaluations.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

DHT may increase the risk of heart disease and death in elderly men.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Dual-targeted therapy is effective and safe for difficult-to-treat inflammatory bowel disease.

Early diagnosis with trichoscopy can improve management and quality of life for CCCA patients.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

Daily subcutaneous testosterone effectively restores testosterone levels in men.

MCTD should be considered in children with recurring muscle issues, lupus-like symptoms, and edema.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

Two sisters had a rare hair condition without other usual symptoms.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Prenatal diagnosis of trichothiodystrophy is possible in the second trimester using fetal eyebrow biopsy, with sulfur content analysis being more reliable.

The folate-cyclodextrin conjugate targets cancer cells more precisely, potentially reducing chemotherapy side effects.

An elemental database for Chinese herbal remedies was created to explore the role of inorganic species in medicine.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Cedrol may be an effective treatment for colorectal cancer.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.