B. J. Clark

发表

GAPDH as a housekeeping gene: analysis of GAPDH mRNA expression in a panel of 72 human tissues.

R. Barber, D. Harmer, R. A. Coleman, 2005, Physiological genomics.

B. J. Clark, 2004 .

The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retina.

P. Luthert, M. Cheetham, B. J. Clark, 2002, Human molecular genetics.

Microbial contamination of cases used for storing contact lenses.

B. J. Clark, L. Harkins, F. A. Munro, 1994, The Journal of infection.

Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2.

M. Gaasenbeek, R. Banerjee, D. Hunt, 2005, Gene.

Metastatic choroidal melanoma to the contralateral orbit 40 years after enucleation.

W. R. Lee, S. Coupland, B. J. Clark, 1996, Archives of ophthalmology.

Muscle changes in the neuroleptic malignant syndrome

D. Mclellan, W. Behan, B. J. Clark, 2000, Journal of clinical pathology.

Protocol for the use of polymerase chain reaction in the detection of intraocular large B-cell lymphoma in ocular samples.

P. Adamson, S. Lightman, B. J. Clark, 2007, The Journal of molecular diagnostics : JMD.

A novel pattern of oculocerebral malformation

W. R. Lee, J. Tolmie, R. Arngrímsson, 1997, The British journal of ophthalmology.

Microbial contamination of contact lens cases in the west of Scotland.

B. J. Clark, C. Abernethy, P. Devonshire, 1993, The British journal of ophthalmology.

Pseudo‐hypopyon as the presenting feature in B‐cell and T‐cell intraocular lymphoma

S. Lightman, B. J. Clark, G. Larkin, 2003, Clinical & experimental ophthalmology.

Orbital lymphoma misdiagnosed as scleritis.

S. Dorey, S. Lightman, B. J. Clark, 2002, Ophthalmology.

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Steve D. M. Brown, S. Cross, I. Jackson, 2002, Human molecular genetics.

Posterior axial corneal malformation and uveoretinal angiodysgenesis — a neurocristopathy?

W. R. Lee, B. J. Clark, C. Mooy, 2007, Graefe's Archive for Clinical and Experimental Ophthalmology.

Pleomorphic lipoma of the orbit: a case series and review of literature.

P. Luthert, B. J. Clark, G. Rose, 2003, Ophthalmology.

Acute postural drop in optic nerve perfusion after vitrectomy and gas in a patient with diabetic autonomic neuropathy

S. Tuft, B. J. Clark, 2022 .

Thrombocytopenia with absent radii (TAR) syndrome: a new increased cellular radiosensitivity syndrome.

P. Bryant, N. Liu, B. J. Clark, 1995, Clinical oncology (Royal College of Radiologists (Great Britain)).

Corneoscleral fibrous histiocytoma

S. Tuft, B. J. Clark, C. Daniel, 2002, The British journal of ophthalmology.

Expression analysis of SIX3 and SIX6 in human tissues reveals differences in expression and a novel correlation between the expression of SIX3 and the genes encoding isocitrate dehyhrogenase and cadherin 18.

I. Hanson, B. J. Clark, V. van Heyningen, 2005, Genomics.

Palisaded encapsulated neuroma (solitary circumscribed neuroma of skin) of the eyelid: report of two cases and review of the literature

S. Dubovy, B. J. Clark, 2001, The British journal of ophthalmology.

The expression of the Leber congenital amaurosis protein AIPL1 coincides with rod and cone photoreceptor development.

Á. Szél, P. Luthert, M. Cheetham, 2003, Investigative ophthalmology & visual science.

Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.

C. Winchester, B. J. Clark, K. Johnson, 1999, Human molecular genetics.

Knowledge of Chlamydia trachomatis genital infection and its consequences in people attending a genitourinary medicine clinic.

S. Capewell, B. J. Clark, R. Hillman, 1999, Sexually transmitted infections.

Control of Gene Expression

B. J. Clark, 2004 .

Abnormal extracellular material in the levator palpebrae superioris complex in congenital ptosis.

W. Behan, B. J. Clark, E. Kemp, 1995, Archives of ophthalmology.

A qualitative review of ptosis surgery

B. J. Clark, E. Kemp, J. Kumar, 1993 .

Absence of SIX6 mutations in microphthalmia, anophthalmia, and coloboma.

A. Christoforou, D. Fitzpatrick, I. Hanson, 2004, Investigative ophthalmology & visual science.

Retinal haemorrhages in an infant following RetCam screening for retinopathy of prematurity

G. Adams, B. J. Clark, S. Fang, 2004, Eye.

Reply to RV Azad et al

G. Adams, B. J. Clark, S. Fang, 2005, Eye.

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma.

M. Fox, S. Povey, P. Khaw, 2000, American journal of human genetics.

Retinal haemorrhages in infant head injury.

P. Luthert, B. J. Clark, G. Adams, 2002, Brain : a journal of neurology.

Sporadic Burkitt's lymphoma presenting as solely orbital disease in a 78-year-old

B. J. Clark, G. Rose, P. Plowman, 2001, Eye.

The expression of the Leber congenital amaurosis protein AIPL1 coincides with rod and cone photoreceptor development.

Á. Szél, P. Luthert, M. Cheetham, 2003, Investigative ophthalmology & visual science.