Search

everythinglearnresearchcommunity

for

Search:↓

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A specific mutation in PA-PLA1α causes abnormal hair growth.

β-catenin, Shh, and Bmp signaling control hair follicle development.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Vitamin D receptor helps control skin cell growth and hair development.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

GIANT improves brain imaging by using genetics to better map brain regions.

Sebaceous glands help study fatty acid transporters and binding proteins.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Zebrafish with mutations similar to human Cantú Syndrome have heart cells with altered channel properties, making them a good model to study the condition.

The Hair Cell Analysis Toolbox automates and improves the analysis of cochlear hair cells using machine learning.

Longer CAG repeats in gene linked to more severe hair loss in females.

The Glu413Lys mutation in keratin affects hair stability, while Glu413Asp does not.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

Rac1 is crucial for normal hair structure and pigmentation.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Genetic profiling can improve androgenetic alopecia treatment by predicting drug response and minimizing side effects.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Gene variations may increase oxidative stress in male pattern baldness.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.