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

Possible link between hair loss and metabolic syndrome, with RANTES as a potential clue.

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.

Benzothiazepines like diltiazem reduce anxiety in mice by making neurosteroids.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

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

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

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 document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.

The document concludes that skin and nail changes can indicate various underlying health conditions.

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

Animal research has greatly advanced dermatology.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Cynoglossum amabile has medicinal potential but poses safety concerns due to liver toxicity.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.