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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Combining hair transplantation with PRP is more effective for treating hair loss than hair transplantation alone.

The buffy coat method yields higher TGF-β1 levels in PRP, especially in males.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

HR protein causes abnormal hair cycles by increasing Tgf-β2 and reducing miR-31.

Polarized Raman spectra can reveal changes in hair keratin's protein structures.

Platelet-rich plasma (PRP) treatments are not effective.

Rice bran extract can help with hair growth, thickness, and color.

PRP may help reduce brain inflammation and protect brain cells.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

PP405 shows promise as a new, effective treatment for hair loss with minimal side effects.

A new method improves protein extraction from hair, helping identify potential biomarkers for fetal growth issues.

The procedure accurately measures 5-alpha-dihydrotestosterone in blood, useful for standard tests.

A specific gene mutation causes a severe skin disorder in a family.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Targeting the p300/AR axis may help treat polycystic ovary syndrome.

rPanglaoDB helps study rare cell types by merging RNA data, showing fibrocytes aid in healing.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

PRP shows promise for spinal pain but needs more guidelines before widespread use.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.