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PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Slug (Snai2) helps regulate hair growth timing in mice.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Cantú syndrome is caused by mutations in the ABCC9 gene.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

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.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

Keratin mutations cause skin diseases and could lead to new treatments.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

High TSPEAR levels in colorectal cancer predict worse outcomes.

A truncated protein linked to breast cancer may change cell adhesion.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

A new gene variant causes curly coats in some dog breeds.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

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

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.