E. Bingham

发表

Macular Degeneration in Individuals with Cone Specific Gene Loss

P. Sieving, J. Felius, R. Ayyagari, 1999 .

Comparison of two decellularized dermal equivalents

H. M. Kim, S. Feinberg, E. Bingham, 2018, Journal of tissue engineering and regenerative medicine.

Differentiation of hES Cells to a Parathyroid-Like Phenotype

K. Ignatoski, G. Doherty, E. Bingham, 2009 .

Differentiation of human embryonic stem cells to a parathyroid-like phenotype.

K. M. Woods Ignatoski, G. Doherty, E. Bingham, 2009, Stem cells and development.

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

P. Sieving, M. R. Young, M. Boehnke, 1990, American journal of human genetics.

Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.

M. Alpern, P. Sieving, F. Naarendorp, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Rearrangement of immunoglobulin and T-cell receptor genes in Hodgkin's disease.

D. Ginsburg, E. Bingham, M. Roth, 1988, The American journal of pathology.

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene.

P. Sieving, B. Ehinger, R. Ayyagari, 2000, Archives of ophthalmology.

Detection of Philadelphia chromosome-positive cells by the polymerase chain reaction following bone marrow transplant for chronic myelogenous leukemia.

D. Ginsburg, E. Bingham, M. Roth, 1989, Blood.

Detection of Philadelphia chromosome-positive cells by the polymerase chain reaction following bone marrow transplant for chronic myelogenous leukemia

D. Ginsburg, E. Bingham, J. Antin, 1989 .

Characterization and expression of H‐2I region gene products on bone marrow‐derived macrophages

D. Gutmann, L. Schook, J. Niederhuber, 1982 .

Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.

K. Lunetta, P. Sieving, M. Boehnke, 1996, Human heredity.

Rearrangement ofImmunoglobulin and T-Cell Receptor Genes in Hodgkin's Disease

D. Ginsburg, E. Bingham, M. Roth, 2007 .

On bone marrow-derived macrophages.

D. Gutmann, L. Schook, E. Bingham, 1982 .

Binding and Internalization of Herpes Simplex Virus‐Antibody Complexes by Polymorphonuclear Leukocytes

E. Bingham, J. Jachimowicz, Jerry W. Smith, 1986, Journal of medical virology.

Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22.

P. Sieving, M. Ross, M. Vaudin, 1999, Genomics.

A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutation.

P. Sieving, B. Shastry, R. Mendoza-Londono, 1999, Ophthalmic genetics.

Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.

P. Sieving, J. Richards, E. Bingham, 1999, American journal of ophthalmology.

A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3.

P. Sieving, J. Ott, M. Devoto, 1996, American journal of human genetics.

Dependence on antibody for induction of chemiluminescence in polymorphonuclear leukocytes by herpes simplex virus.

E. Bingham, A. Sugar, J. Smith, 1985, Investigative ophthalmology & visual science.

Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

P. Sieving, A. Ballabio, T. Rosenberg, 1998 .

X-linked recessive atrophic macular degeneration from RPGR mutation.

P. Sieving, M. Boehnke, H. Stringham, 2002, Genomics.

Clinical course and visual function in a family with mutations in the RPE65 gene.

P. Sieving, J. Felius, N. Khan, 2002, Archives of ophthalmology.

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

P. Sieving, J. Felius, R. Ayyagari, 1999, Molecular vision.

USE OF POLYMERASE CHAIN REACTION‐DETECTED SEQUENCE POLYMORPHISMS TO DOCUMENT ENGRAFTMENT FOLLOWING ALLOGENEIC BONE MARROW TRANSPLANTATION

D. Ginsburg, E. Bingham, M. Roth, 1990, Transplantation.

Bietti crystalline retinopathy and juvenile retinoschisis in a family with a novel RS1 mutation.

P. Sieving, L. Jampol, E. Bingham, 2001, A M A Archives of Ophthalmology.

Searching for Genotype-Phenotype Correlations in X-Linked Juvenile Retinoschisis

P. Sieving, B. Yashar, R. Ayyagari, 2001 .

Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

P. Sieving, G. Fishman, B. Yashar, 1999, Human mutation.

Refined genetic mapping of juvenile X-linked retinoschisis.

K. Lunetta, P. Sieving, M. Boehnke, 1995, Human heredity.

Differentiation of precursors into parathyroid-like cells for treatment of hypoparathyroidism.

K. M. Woods Ignatoski, G. Doherty, E. Bingham, 2010, Surgery.

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy

P. Sieving, J. Felius, R. Ayyagari, 2000, Human Genetics.

Blue Cone Monochromacy

P. Sieving, J. Felius, R. Ayyagari, 1999 .

Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.

P. Sieving, S. Jacobson, B. Lorenz, 2000, Investigative ophthalmology & visual science.

Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.

P. Sieving, S. Moroi, R. Ayyagari, 2000, Archives of ophthalmology.

SORSBY'S DYSTROPHY IN A FAMILY WITH A SER-181-CVS MUrATION IN THE TIMP-3 GENE: POOR OUTCOME AFTER LASER PHOTOCOAGULATION*

P. Sieving, E. Bingham, S. Boskovich, 2005 .

X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC.

P. Sieving, J. Richards, E. Bingham, 1996, Human heredity.

Fabrication of Large Size Ex Vivo-Produced Oral Mucosal Equivalents for Clinical Application.

S. Feinberg, E. Bingham, H. Kato, 2015, Tissue engineering. Part C, Methods.

Rapid Self‐Assembly of Macroscale Tissue Constructs at Biphasic Aqueous Interfaces

Brendan M Leung, S. Takayama, H. T. Sarhan, 2015 .

The MHC Restriction of a Monoclonal Antigen-Specific I-J + TsF 2 Maps to a Location Outside the I-J Subregion

J. Niederhuber, E. Bingham, E. Dugan, 1983 .

Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.

P. Sieving, E. Bingham, H. Pawar, 1996, Transactions of the American Ophthalmological Society.