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A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

BFNB could be a promising treatment for hair growth.

Defective nuclear transport may cause gene expression changes in Progeria.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Tyrosinase and gp100 proteins can help diagnose and treat melanoma.

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

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

Hair proteins have weak spots in their α-helical segments.

Rhus semialata gall extract and Penta-O-Galloyl-β-D-Glucose may effectively reduce hair loss.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Hair structural proteins are synthesized sequentially in specific cells, offering a new way to study hair proteins and defects.

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

Family members have similar hair protein patterns, which could be useful for genetic studies.

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

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Specific keratin gene mutations can cause monilethrix.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

BAF200 is essential for proper heart and coronary artery formation.

Bone Morphogenetic Proteins (BMPs) are important for hair growth, and their decrease due to hormones could lead to hair loss, but adding more BMPs could promote hair growth.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.