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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The document concludes that stem cell inactivity is actively controlled and important for tissue repair and balance.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

Male tissue has more cell death than female tissue after ischemia, and some neurosteroids only protect female cells.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Bimatoprost increases hair growth in mice without breaking down into other substances.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

A woman with a rare scalp lymphoma had unusual hair loss after treatment.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

Finasteride helps treat skin issues like acne and baldness by blocking testosterone conversion.

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

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

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

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

The document does not determine if adults with aphallia are fertile.

Different types of skin stem cells can change and adapt, which is important for developing new treatments.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

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.

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

Dental pulp stem cells might not reliably become neurons.