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Generalized glucocorticoid resistance causes hormone imbalances and varied symptoms due to gene mutations.

A 78-year-old man with Cronkhite-Canada syndrome improved significantly after treatment and remains symptom-free.

The protocol allows easy imaging of dividing cells in C. elegans and can be used for other organisms.

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.

CDP is crucial for lung and hair follicle cell development.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Hair testing can detect a single GHB exposure, useful for documenting sexual assault.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Trichohyalin granules help inner root sheath cells in hair follicles harden by integrating with keratin filaments.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

The updated GRADE guidance advises considering context when interpreting variability in research results and introduces tools for assessing subgroup effects.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Activated LEF/TCF complexes are crucial for hair development and cycling.

NFIC helps rat dental cells grow and turn into bone-like cells.

High Geh gene expression in Staphylococcus aureus contributes to acne.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.