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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

The mutation helps mice handle heat better without affecting hair growth.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

NIPP1 is important for healthy skin and could help treat skin inflammation.

PINCH-1 is crucial for skin cell adhesion and movement, working with EPLIN and ILK.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

LHX2 is crucial for development, tissue repair, and preventing diseases.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Different Myc family proteins are located in various parts of the hair follicle and may affect stem cell behavior.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

mTORC2 is crucial for healthy skin barrier by regulating lipids and filaggrin.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

Zfp462 deficiency in mice causes anxiety-like behaviors and excessive self-grooming.

Rac1 is essential for proper hair structure and color.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Hair loss in certain mice is linked to changes in keratin-related genes.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.