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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.

The method successfully created stable transfection donor cells for goat hair follicle research.

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Sheep cells were successfully modified to include a spider silk protein gene.

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Latanoprost eye drops caused excessive hair growth and eyelash whitening in a woman.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

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Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

A specific genetic variation affects wool quality in sheep.

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High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

Lhx2 helps retinal cells respond to signals for eye development.

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LHX2 is crucial for development, tissue repair, and preventing diseases.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Latanoprost 0.1% may effectively treat hair loss.

Researchers created a system that accurately aligns laser beams automatically.

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New laser particles can track thousands of cells in 3D models, improving single-cell analysis.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

No significant link was found between the rs1998076 gene variant and hair loss in Indonesians.

LX-38 is a safer drug option for hair loss and prostate issues without hormonal side effects.

The scraggly mutation causes hair loss and skin defects in mice.