Search

everythinglearnresearchcommunity

for

Search:↓

CircAGK affects cell death in hair cells by controlling the miR-3180-5p/BAX pathway, which can lead to hair loss.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Keratinocyte growth factor significantly alters skin and tissue development.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

DSDs are birth conditions causing unusual sex development, managed with personalized care and sometimes surgery, but still lack a standard treatment approach.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

Metabolic processes and key genes like FGF5, FGFR1, and RRAS significantly affect hair follicle growth in Inner Mongolian Cashmere goats.

Two new gene mutations cause a rare hair disorder.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

SGK3 is essential for proper hair growth and health.

Researchers found a gene mutation responsible for a rare hair loss condition.

FGFR2 signaling controls Merkel cell formation in different skin regions.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

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

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

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Blocking autophagy increases survival of inner ear hair cells exposed to gentamicin.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Dahuang-Gancao Decoction improves hair growth in androgenetic alopecia.

Researchers found three types of melanocytes in developing mouse skin, each with different genes and locations.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

EGFR is essential for normal hair development and follicle differentiation.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.