Dr. John J Harding MD
Psychiatrist | Psychiatry
100 E Lehigh Ave Mab Bldg, Suite 105 Philadelphia PA, 19125About
Dr. John Harding is a psychiatrist practicing in Philadelphia, PA. Dr. Harding is a medical doctor specializing in the care of mental health patients. As a psychiatrist, Dr. Harding diagnoses and treats mental illnesses. Dr. Harding may treat patients through a variety of methods including medications, psychotherapy or talk therapy, psychosocial interventions and more, depending on each individual case. Different medications that a psychiatrist might prescribe include antidepressants, antipsychotic mediations, mood stabilizers, stimulants, sedatives and hypnotics. Dr. Harding treats conditions like depression, anxiety, OCD, eating disorders, bipolar disorders, personality disorders, insomnia, ADD and other mental illnesses.
Education and Training
Temple Univ Sch of Med, Philadelphia Pa 1973
Temple University School of Medicine 1973
Board Certification
Psychiatry and NeurologyAmerican Board of Psychiatry and NeurologyABPN
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Protective effects of ibuprofen and its major metabolites against in vitro
- Effects of modifications of alpha-crystallin on its chaperone and other properties.
- The effect of modification of alpha-crystallin by prednisolone-21-hemisuccinate and fructose 6-phosphate on chaperone activity.
- Viewing molecular mechanisms of ageing through a lens.
- Enzyme activity after resealing within ghost erythrocyte cells, and protection by alpha-crystallin against fructose-induced inactivation.
- The molecular chaperone alpha-crystallin incorporated into red cell ghosts protects membrane Na/K-ATPase against glycation and oxidative stress.
- Gamma III-crystallin is the primary target of glycation in the bovine lens
- The molecular chaperone, alpha-crystallin, protects against loss of antigenicity and activity of esterase caused by sugars, sugar phosphate and a steroid.
- The identification of a reaction site of glutathione mixed-disulphide formation on gammaS-crystallin in human lens.
- Revival of inactive glyceraldehyde 3-phosphate dehydrogenase in human cataract
- Trehalose and 6-aminohexanoic acid stabilize and renature glucose-6-phosphate dehydrogenase inactivated by glycation and by guanidinium hydrochloride.
- Carnosine protects against the inactivation of esterase induced by glycation and a steroid.
- Glutathione reductase from human cataract lenses can be revived by reducing agents and by a molecular chaperone, alpha-crystallin.
- Glutathione-related enzymes and the eye.
- Carnosine inhibits modifications and decreased molecular chaperone activity of lens alpha-crystallin induced by ribose and fructose 6-phosphate.
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