Search

everythinglearnresearchcommunity

for

Search:↓

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Blocking DGAT1 reduces oil gland size in mice and dogs, but only mice experience hair loss.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Photodynamic therapy may not work for erythroplasia of Queyrat and could lead to invasive squamous cell carcinoma.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

FLCN helps control iron levels in cells.

CD4+ skin cells may be precursors to basal cell carcinoma.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

OM-X® helped prevent negative effects of Vitamin C deficiency in mice, suggesting it could protect organs and regulate metabolism.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

FGF18 treatment during hair's resting phase can protect against hair loss from radiation.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.