Search

everythinglearnresearchcommunity

for

Search:↓

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

CAG repeat numbers in the AR gene likely don't affect male pattern baldness in Korean men.

GKLF/KLF4 and Sp1 control Keratin 19 gene activity, influencing cancer-related changes.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A mutation in the KRT74 gene causes tightly curled hair.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

CDK4/6 inhibitors affect safety and quality of life differently, requiring careful use.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Keratins 6, 16, and 17 increase in damaged or diseased skin and may help diagnose skin issues.

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

Understanding the APCDD1 gene can lead to new hair loss treatments.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

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

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Two new gene clusters important for hair formation were found on human chromosome 11.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.