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Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

The 2024 guideline updates recommendations for genetic testing, imaging, and sperm retrieval in male infertility.

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.

Certain gene variations are not a major cause of male infertility in Nigerian men.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Finasteride may negatively affect male fertility.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

DA-9401 helps protect rat testis from finasteride damage.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Hair changes can indicate systemic diseases or medication effects.

Finasteride may cause sexual side effects like erectile dysfunction, but they are reversible and affect less than 2% of men.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

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.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

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

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

New genetic mutations linked to rare skin disorders were found in three newborns.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.