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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Mutations in the SNRPE gene cause hereditary hair loss.

TTD patients don't have a higher skin cancer risk because their main issue is with transcription, not DNA repair.

TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

TR3 is mainly found in hair follicle stem cells and may be involved in hair loss.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Thioredoxin reductase 1 does not affect glucocorticoid receptor activity in hair follicle cells.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Targeting METTL1 may help slow papillary thyroid cancer growth and spread.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.