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The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Estrogens can improve skin aging but carry risks; more research is needed on safer treatments.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

Estrogens generally inhibit hair growth and improve skin quality, but their exact effects on hair follicles are complex and not fully understood.

New treatments targeting skin stem cells show promise for skin repair, anti-aging, and cancer therapy.

Two gene areas linked to male pattern baldness found, more research needed.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Some skin diseases and their treatments can negatively affect male fertility.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Finasteride, often used for hair loss, can potentially cause cataracts.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

S100A3 protein is crucial for hair shaft formation in mice.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.