O. Sundin

R. McCallum, D. Díaz-Arévalo, J. Ordoñez, 2018, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.

A missense mutation in GUCY2Dacts as a genetic modifier in RPE65-related Leber Congenital Amaurosis

E. Traboulsi, R. Koenekoop, I. Maumenee, 2004 .

A missense mutation in GUCY2D acts as a genetic modifier in RPE65-related Leber Congenital Amaurosis.

E. Traboulsi, R. Koenekoop, I. Maumenee, 2004, Ophthalmic genetics.

The Mouse's Eye and Mfrp: Not Quite Human

O. Sundin, 2005, Ophthalmic genetics.

A spontaneous mutation affects programmed cell death during development of the rat eye.

C. Zhang, M. Goldberg, T. O'brien, 2005, Experimental eye research.

Mo1857 Role of PCR Amplification of Jejunal Aspirates in Relation to Culture and Breath Test in the Diagnosis of Small Intestinal Bacterial Overgrowth

R. McCallum, D. Díaz-Arévalo, M. Zeng, 2015 .

A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype.

Y. Li, I. Maumenee, O. Sundin, 2000, Investigative ophthalmology & visual science.

14C2H4 Metabolism in Morning Glory Flowers

O. Sundin, E. Beyer, 1978 .

C(2)H(4) metabolism in morning glory flowers.

O. Sundin, E. Beyer, 1978, Plant physiology.

Immunohistochemistry and electron microscopy of early-onset fuchs corneal dystrophy in three cases with the same L450W COL8A2 mutation.

W. Green, J. Gottsch, Z. C. de la Cruz, 2006, Transactions of the American Ophthalmological Society.

Terminal stages of SV40 DNA replication proceed via multiply intertwined catenated dimers

A. Varshavsky, O. Sundin, 1980, Cell.

Arrest of segregation leads to accumulation of highly intertwined catenated dimers: Dissection of the final stages of SV40 DNA replication

A. Varshavsky, O. Sundin, 1981, Cell.

Staphylococcal nuclease makes a single non-random cut in the simian virus 40 viral minichromosome.

A. Varshavsky, O. Sundin, 1979, Journal of molecular biology.

Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene.

Cheng Zhang, W. Green, J. Gottsch, 2005, Investigative ophthalmology & visual science.

Inheritance of a novel COL8A2 mutation defines a distinct early-onset subtype of fuchs corneal dystrophy.

K. Broman, A. Jun, J. Gottsch, 2005, Investigative ophthalmology & visual science.

The Pax-6 homeobox gene is expressed throughout the corneal and conjunctival epithelia.

O. Sundin, B. Koroma, J. M. Yang, 1997, Investigative ophthalmology & visual science.

Analysis and Documentation of Progression of Fuchs Corneal Dystrophy With Retroillumination Photography

D. Emmert, J. Gottsch, G. W. Schmidt, 2006, Cornea.

A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.

K. Broman, J. Gottsch, W. Stark, 2006, Investigative ophthalmology & visual science.

Inheritance of a Novel COL8A2 Mutation Defines a Distinct Subtype of Fuchs' Corneal Dystrophy

K. Broman, A. Jun, J. Gottsch, 2005 .

A stretch of “late” SV40 viral DNA about 400 bp long which includes the origin of replication is specifically exposed in SV40 minichromosomes

A. Varshavsky, O. Sundin, M. Bohn, 1979, Cell.

Sequence and location of SIX3, a homeobox gene expressed in the human eye.

O. Sundin, J. M. Yang, G. Leppert, 1999, Ophthalmic genetics.

Genetic basis of total colourblindness among the Pingelapese islanders

I. Maumenee, Eduardo D. Silva, O. Sundin, 2000, Nature Genetics.

Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.

K. Broman, J. Sunness, J. Toy, 2005, Proceedings of the National Academy of Sciences of the United States of America.

The optx2 homeobox gene is expressed in early precursors of the eye and activates retina-specific genes.

J. Toy, O. Sundin, Jun-ming Yang, 1998, Proceedings of the National Academy of Sciences of the United States of America.

The human jejunum has an endogenous microbiota that differs from those in the oral cavity and colon

R. McCallum, D. Díaz-Arévalo, J. Ordoñez, 2017, BMC Microbiology.

Pax-6 is first expressed in a region of ectoderm anterior to the early neural plate: implications for stepwise determination of the lens.

D. Pasko, O. Sundin, Jun-ming Yang, 1994, Developmental biology.

Pax-6, Prox 1, and Chx10 homeobox gene expression correlates with phenotypic fate of retinal precursor cells.

R. Mcinnes, T. Belecky-Adams, R. Adler, 1997, Investigative ophthalmology & visual science.

Molecular approaches to vertebrate limb morphogenesis.

G. Eichele, C. Thaller, K. Pang, 1989, Development.

Chicken homeobox gene prox 1 related to Drosophila prospero is expressed in the developing lens and retina

J. Piatigorsky, S. Banerjee-Basu, M. Duncan, 1996, Developmental dynamics : an official publication of the American Association of Anatomists.

SV40 viral minichromosome: preferential exposure of the origin of replication as probed by restriction endonucleases.

A. Varshavsky, O. Sundin, M. Bohn, 1978, Nucleic acids research.

Optic nerve aplasia in an infant with congenital hypopituitarism and posterior pituitary ectopia.

M. Brodsky, Sean-Paul A Atreides, J. Fowlkes, 2004, Archives of ophthalmology.

11 – Retinoids and Pattern Formation in Vertebrate Embryos

G. Eichele, O. Sundin, R. Janocha, 1993 .

Cellular and SV40 chromatin: replication, segregation, ubiquitination, nuclease-hypersensitive sites, HMG-containing nucleosomes, and heterochromatin-specific protein.

J. Barsoum, E. Ozkaynak, D. Finley, 1983, Cold Spring Harbor symposia on quantitative biology.

Genetics of Fuchs Corneal Dystrophy Comes of Age: Sweet Repeats.

O. Sundin, 2015, JAMA ophthalmology.

Developmental Basis of Nanophthalmos: MFRP Is Required for both Prenatal Ocular Growth and Postnatal Emmetropization

I. Bhutto, G. Lutty, I. Maumenee, 2008, Ophthalmic genetics.

Efficacy of topical dorzolamide therapy for cystoid macular edema in a patient with MFRP-related nanophthalmos-retinitis pigmentosa-foveoschisis-optic disk drusen syndrome.

R. Susanna, W. Takahashi, Bianca N. Susanna, 2015, Retinal cases & brief reports.

Novel membrane frizzled‐related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds

J. Verheij, E. Morales, O. Sundin, 2014, Acta ophthalmologica.

Posterior Polar Cataract: Genetic Analysis of a Large Family

I. Maumenee, J. Sallum, O. Sundin, 2005, Ophthalmic genetics.

The human jejunum has an endogenous microbiota that differs from those in the oral cavity and colon

R. McCallum, D. Díaz-Arévalo, J. Ordoñez, 2017, BMC Microbiology.

A new human retinal pigment epithelial cell model for interrogating the protective functions of xanthophylls in retinopathies (39.2)

Xiaoming Gong, L. Rubin, O. Sundin, 2014 .

A Spontaneous Missense Mutation in Branched Chain Keto Acid Dehydrogenase Kinase in the Rat Affects Both the Central and Peripheral Nervous Systems

S. Mori, K. Broman, D. Goldman, 2016, PloS one.

A G1103R Mutation in CRB1 is Co-Inherited with High Hyperopia and Leber Congenital Amaurosis

I. Maumenee, H. Abouzeid, O. Sundin, 2006, Ophthalmic genetics.

Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene.

J. Gottsch, O. Sundin, Cheng Zhang, 2005, Investigative ophthalmology & visual science.

Mutational analysis and clinical correlation in Leber congenital amaurosis

E. Traboulsi, R. Koenekoop, I. Maumenee, 2000, Ophthalmic genetics.

Expression of the Optx2 homeobox gene during mouse development

J. Toy, O. Sundin, Jeffrey Toya, 1999, Mechanisms of Development.