Anophthalmia Plus Syndrome Latest Advances

Inducible Calling Cards: Developing Mouse Reagents for Experimentally Controlled Transposon Insertion in vivo.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Anophthalmic Sockets: A Retrospective Review of Enucleations, Eviscerations, and Exenterations Performed and Managed in a Tertiary Care Hospital.

Journal: Journal of clinical medicine

Published: September 18, 2025

Congenital anophthalmia treated with a dermis fat graft combined with a skin graft in the upper lid in early childhood.

Journal: Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society

Published: September 06, 2025

NOA1 deficiency observed in a subset of Montbéliarde calves with bilateral anophthalmia.

Journal: Animal genetics

Published: August 28, 2025

The evaluation and management of dry anophthalmic socket syndrome.

Journal: Survey of ophthalmology

Published: August 25, 2025

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Journal: Research square

Published: July 09, 2025

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Journal: Communications biology

Published: June 16, 2025

Thyroid hormone receptor blockade by amiodarone disrupts angiogenesis via VEGFα, WNT7A, BMP, and PI3K/AKT pathways in chick embryo vascular development.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: May 24, 2025

Ophthalmologic Findings in an Induced Model of Holoprosencephaly in Zebrafish.

Journal: The Journal of comparative neurology

Published: May 15, 2025

Genotypic and phenotypic spectrum of anophthalmia/microphthalmia in families from Khyber Pakhtunkhwa, Pakistan.

Journal: Journal of human genetics

Published: May 07, 2025

Whole Exome Sequencing Helps Diagnose Familial Anophthalmia in Zimbabwe: A Call from the Field to Fund Clinical Genomics for Planetary Health.

Journal: Omics : a journal of integrative biology

Published: April 11, 2025

A Homozygous Mutation (c.241G > A, p.A81T) in the Calsequestrin-2 Causes Eye Defects in Zebrafish.

Journal: Biochemical genetics

Published: April 07, 2025

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Inducible Calling Cards: Developing Mouse Reagents for Experimentally Controlled Transposon Insertion in vivo.

Inducible Calling Cards: Developing Mouse Reagents for Experimentally Controlled Transposon Insertion in vivo.

Anophthalmic Sockets: A Retrospective Review of Enucleations, Eviscerations, and Exenterations Performed and Managed in a Tertiary Care Hospital.

Anophthalmic Sockets: A Retrospective Review of Enucleations, Eviscerations, and Exenterations Performed and Managed in a Tertiary Care Hospital.

Congenital anophthalmia treated with a dermis fat graft combined with a skin graft in the upper lid in early childhood.

Congenital anophthalmia treated with a dermis fat graft combined with a skin graft in the upper lid in early childhood.

NOA1 deficiency observed in a subset of Montbéliarde calves with bilateral anophthalmia.

NOA1 deficiency observed in a subset of Montbéliarde calves with bilateral anophthalmia.

The evaluation and management of dry anophthalmic socket syndrome.

The evaluation and management of dry anophthalmic socket syndrome.

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Dnmt3a2 expression during embryonic development is required for phenotypic stability.

Thyroid hormone receptor blockade by amiodarone disrupts angiogenesis via VEGFα, WNT7A, BMP, and PI3K/AKT pathways in chick embryo vascular development.

Thyroid hormone receptor blockade by amiodarone disrupts angiogenesis via VEGFα, WNT7A, BMP, and PI3K/AKT pathways in chick embryo vascular development.

Ophthalmologic Findings in an Induced Model of Holoprosencephaly in Zebrafish.

Ophthalmologic Findings in an Induced Model of Holoprosencephaly in Zebrafish.

Genotypic and phenotypic spectrum of anophthalmia/microphthalmia in families from Khyber Pakhtunkhwa, Pakistan.

Genotypic and phenotypic spectrum of anophthalmia/microphthalmia in families from Khyber Pakhtunkhwa, Pakistan.

Whole Exome Sequencing Helps Diagnose Familial Anophthalmia in Zimbabwe: A Call from the Field to Fund Clinical Genomics for Planetary Health.

Whole Exome Sequencing Helps Diagnose Familial Anophthalmia in Zimbabwe: A Call from the Field to Fund Clinical Genomics for Planetary Health.

A Homozygous Mutation (c.241G > A, p.A81T) in the Calsequestrin-2 Causes Eye Defects in Zebrafish.

A Homozygous Mutation (c.241G > A, p.A81T) in the Calsequestrin-2 Causes Eye Defects in Zebrafish.