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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

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

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The Paxbp1 gene is crucial for healthy hair follicles.

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

BLMP-1 is important for regular molting and gene expression cycles in worms.

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

Targeting ornithine decarboxylase can help prevent skin cancer.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

BMAL1 controls skin cell growth and UV damage risk, peaking at night.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.