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Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Understanding how epigenetic regulation affects stem cells is key to cancer insights and new treatments.

Mice can regenerate ear tissue without the p53 protein.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Researchers found a new mutation causing total hair loss from birth.

Mechlorethamine treatment regrew hair in mice by killing immune cells causing hair loss without harming hair follicles.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

No link found between specific genes and female pattern hair loss.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Mild essential fatty acid deficiency can cause health issues and is worsened by low-fat diets.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Early balding at 40 increases prostate cancer risk.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Old treatments for other skin conditions showed promise for hair regrowth in mice with a hair loss condition.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The document concludes that pregnancy and cancer share immune evasion tactics, but more research is needed before using checkpoint blockade immunotherapy in pregnant cancer patients to avoid harm to the placenta.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Two-photon microscopy effectively tracks live stem cell activity in mouse skin with minimal harm and clear images.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.