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

Overexpressing IGF-1 in mice leads to skin abnormalities and tumors.

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

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Vinblastine can help treat childhood ITP but may cause reversible side effects.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Tocilizumab might be an effective treatment for COVID-19.

BCG site reactions after COVID-19 mRNA vaccination are mild, temporary, and likely under-reported.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

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

A standardized scoring system is needed to improve model reliability for predicting hair loss in brain tumor patients treated with proton therapy.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Inhibiting TYK2 can restore hair growth in alopecia areata.

An isolated episcleral plasmacytoma can mimic episcleritis, making diagnosis challenging.

PROTAC technology shows promise for cancer treatment but needs more effective E3 ligase recruiters.

Thymosin β4 and VEGF are important for blood vessel formation in many organs.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

Overexpressing Tβ4 in cashmere goats improves hair fiber traits and increases cashmere yield.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Telomerase-positive cells are mainly in the bulb matrix and outer root sheath of hair follicles.

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

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Increasing Treg cells in the skin does not cure hair loss from alopecia areata in mice.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.