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8 works

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BOOKS

Books

1 total

Gene . The Universal Calf, by Drs. L. N. Hazel and L. E. Johnson.

L. N. Hazel

zipen1956

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DOCUMENTS · SCRIBD

Documents

12 total

ABCC2 Gene and Dubin-Johnson Syndrome

Yairt Toledo De Los Santos

Appeal Affirmed: Harold Lee v. Gene Johnson

Scribd Government Docs

Barry Hall v. Gene Johnson Appeal Decision

Scribd Government Docs

Maxie Thaniel v. Gene Johnson Appeal Dismissed

Scribd Government Docs

Leonard Brown v. Gene Johnson Appeal Dismissed

Scribd Government Docs

Ivan Sparks v. Gene Johnson Appeal Decision

Scribd Government Docs

Sharn Jackson v. Gene Johnson Appeal Dismissed

Scribd Government Docs

RESEARCH ARTICLES

Research articles

12 total

Altered Retinoid Metabolism Gene Expression in Chronic Stevens-Johnson Syndrome

Srividya, Gurumurthy

British Journal of Ophthalmology2019

DOI 10.1136/bjophthalmol-2018-312849

Altered Retinoid Metabolism Gene Expression in Chronic Stevens-Johnson Syndrome

Srividya, Gurumurthy

BMJ Publishing Group2019

DOI 10.1136/bjophthalmol-2018-312849

Association of Fas Ligand Gene Polymorphism with Stevens-Johnson Syndrome

Ueta, M

BMJ Publishing Group2008

DOI 10.1136/bjo.2007.136796

Molecular Evidence of Triplication in the Haptoglobin Johnson Variant Gene

Salvatore Oliviero

Springer1985

DOI 10.1007/bf00295668

Epithelial Hyperproliferation and Transglutaminase 1 Gene Expression in Stevens-Johnson Syndrome Conjunctiva

Kohji Nishida

American Society for Investigative Pathology1999

DOI 10.1016/s0002-9440(10)65279-0

Toll-like Receptor 3 Gene Polymorphisms in Japanese Patients with Stevens-Johnson Syndrome

Ueta, M.

BMJ Publishing Group2007

DOI 10.1136/bjo.2006.113449

Mutation analysis of the ABCC2 gene in Chinese patients with Dubin‐Johnson syndrome

Wu, Lina

Spandidos Publications2018

DOI 10.3892/etm.2018.6682

Investigation of Mannose-binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens Johnson Syndrome and Stevens Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome

Karkucak, Mutlu

Galenos Yayinevi2012

DOI 10.5152/balkanmedj.2012.018

Gene Expression Analysis of Conjunctival Epithelium of Patients with Stevens-Johnson Syndrome in the Chronic Stage

Ueta, Mayumi

BMJ2019

DOI 10.1136/bmjophth-2018-000254

A Mutation in the Human Canalicular Multispecific Organic Anion Transporter Gene Causes the Dubin-Johnson Syndrome

C Paulusma

Ovid Technologies (Wolters Kluwer Health)1997

DOI 10.1002/hep.510250635

Neonatal Dubin-Johnson Syndrome: Novel Compound Heterozygous Mutation in the ABCC2 Gene

Okada, Hitoshi

Pediatrics International2014

DOI 10.1111/ped.12404

Novel Mutations in the Dubin–Johnson Syndrome Gene ABCC2/MRP2 and Associated Biochemical Changes

Devgun, M. S.

Royal Society of Medicine Press2012

DOI 10.1258/acb.2012.011279