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The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Low oxygen areas help maintain and protect blood stem cells by using a simple sugar breakdown process for energy and managing their activity levels.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Hairless protein can block vitamin D activation in skin cells.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

New therapies are being developed that target integrin pathways to treat various diseases.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

CD8+ T cells are involved in alopecia areata and may cause disease relapse.

Notch signaling disruptions can cause various skin diseases.

VDR regulation varies by tissue and is crucial for its biological functions.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

TLR4 is important in aging-related diseases and could be a new treatment target.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Fusion proteins can protect hair from heat damage.