F J Smith Selected Research

Hereditary Corneal Dystrophies

1/2000

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

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F J Smith Research Topics

Disease

6	Pachyonychia Congenita (Jadassohn-Lewandowsky Syndrome) 07/2021 - 06/2000
2	Type 1 Diabetes Mellitus (Autoimmune Diabetes) 04/2012 - 04/2010
1	Juvenile Arthritis (Juvenile Idiopathic Arthritis) 10/2016
1	Chronic Obstructive Pulmonary Disease (COPD) 01/2015
1	Chronic Disease (Chronic Diseases) 10/2008
1	Cysts 12/2001
1	Loose Anagen Hair Syndrome 10/2001
1	Malformed Nails (Pachyonychia) 05/2001
1	Epidermolysis Bullosa Simplex (Epidermolysis Bullosa Herpetiformis Dowling Meara) 05/2001
1	Weight Loss (Weight Reduction) 11/2000
1	Body Weight (Weight, Body) 11/2000
1	Ichthyosis Bullosa of Siemens 11/2000
1	Hyperkeratosis of the palms and soles and esophageal papillomas 06/2000
1	Hereditary Corneal Dystrophies 01/2000

Drug/Important Bio-Agent (IBA)

7	Keratins (Keratin)IBA 07/2021 - 01/2000
2	Insulin (Novolin)FDA Link 04/2012 - 04/2010
2	Keratin-16 (Keratin 16)IBA 05/2001 - 06/2000
1	A-factor (Streptomyces)IBA 10/2016
1	Dosage Forms (Dosage Form)IBA 10/2008
1	Indicators and Reagents (Reagents)IBA 12/2001
1	DNA (Deoxyribonucleic Acid)IBA 12/2001
1	Keratin-17 (Keratin 17)IBA 05/2001
1	Peptides (Polypeptides)IBA 05/2001
1	pegylated leptinIBA 11/2000
1	Triglycerides (Triacylglycerol)IBA 11/2000
1	Keratin-2 (Keratin 2)IBA 11/2000
1	Proteins (Proteins, Gene)FDA Link 06/2000
1	Keratin-12 (Keratin 12)IBA 01/2000

Therapy/Procedure

2	Therapeutics 01/2015 - 04/2012
1	Injections 04/2010