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Y Indo Selected Research

Monosomy

9/2000Complete paternal uniparental isodisomy for chromosome 1 revealed by mutation analyses of the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with congenital insensitivity to pain with anhidrosis.

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Y Indo Research Topics

Disease

8Hereditary Sensory and Autonomic Neuropathies (HSAN)
10/2012 - 01/2000
6Inborn Genetic Diseases (Disease, Hereditary)
10/2012 - 01/2000
6Hypohidrosis
10/2012 - 01/2000
4Pain (Aches)
10/2012 - 02/2000
4Intellectual Disability (Idiocy)
10/2012 - 01/2000
2Fever (Fevers)
08/2005 - 12/2001
2Self Mutilation
08/2005 - 12/2001
2Uniparental Disomy
10/2001 - 09/2000
1Congenital Pain Insensitivity
10/2012
1Inflammation (Inflammations)
10/2012
1Muscular Diseases (Myopathy)
08/2005
1Deglutition Disorders (Dysphagia)
08/2005
1Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital)
08/2005
1Pyruvate Kinase Deficiency of Red Cells
10/2001
1Complex Regional Pain Syndromes
02/2001
1Monosomy
09/2000
1Bone Fractures (Bone Fracture)
02/2000
1Hyperthermia
02/2000
1Amyloidosis
02/2000

Drug/Important Bio-Agent (IBA)

83-(2-carboxyindol-3-yl)propionic acidIBA
10/2012 - 01/2000
6Nerve Growth Factor (NGF)IBA
10/2012 - 01/2000
3Receptor Protein-Tyrosine Kinases (Tyrosine Kinase Receptors)IBA
12/2001 - 09/2000
1Proteins (Proteins, Gene)FDA Link
10/2012
1Phosphotransferases (Kinase)IBA
02/2001
1tyrosine receptor (receptor, tyrosine)IBA
02/2001
1Pharmaceutical PreparationsIBA
02/2001
1Nerve Growth Factors (Neurotrophins)IBA
02/2000
1Nerve Growth Factor Receptor (Nerve Growth Factor Receptor, Low Affinity)IBA
02/2000