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Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Skin RAGE levels are linked to inflammation and cell death.

Mitochondrial therapy and platelet-rich plasma therapy both stimulated hair regrowth in aging mice, with mitochondrial therapy showing similar effectiveness to plasma therapy.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

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

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

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

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Mechanical forces are crucial for shaping cells and forming tissues during development.

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.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

Certain DNA regions in alpacas are linked to fiber diameter.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Plant extracts like Avicennia marina, Boehmeria nipononivea, and Camellia sinensis could potentially treat hair loss with fewer side effects than synthetic drugs.

High doses of Lepidium sativum seed extract are toxic and should be used with caution.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Epigenetic mechanisms control skin development by regulating gene expression.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Platelet-rich plasma may not be very effective for bone healing and hair growth due to a substance it contains that blocks these processes.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.