Search

everythinglearnresearchcommunity

for

Search:↓

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Over half of the children had abnormal hair under a microscope, with many having genetic hair 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.

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.

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

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.

Taking Propecia might lead to the development of cataracts.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Finasteride causes harmful organ changes in female mice.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

The research identified genes and pathways important for sheep wool growth and shedding.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A gene mutation in mice causes permanent hair loss and skin issues.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

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

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

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

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

New genes linked to male pattern baldness were found on chromosome 20p11.

Certain genes are linked to the risk of developing Alopecia Areata.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.