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J L Chaussain Selected Research

Cytochrome P-450 CYP11B2 (CYP11B2)

7/2001Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia.

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J L Chaussain Research Topics

Disease

2Precocious Puberty
01/2002 - 07/2000
2Congenital Adrenal Hyperplasia (Hyperplasia, Congenital Adrenal)
07/2001 - 01/2001
2Adrenal Insufficiency (Adrenal Gland Hypofunction)
11/2000 - 08/2000
2Esophageal Achalasia (Megaesophagus)
11/2000 - 08/2000
2Achalasia Addisonianism Alacrimia syndrome
11/2000 - 08/2000
1Hyperplasia
07/2001
1And Genital Anomalies Adrenal Hypoplasia Congenita Metaphyseal Dysplasia Intrauterine Growth Retardation
01/2001
1Alacrima
11/2000
1Pituitary Dwarfism
10/2000

Drug/Important Bio-Agent (IBA)

3Adrenocorticotropic Hormone (ACTH)FDA Link
01/2001 - 08/2000
2Gonadotropin-Releasing Hormone (GnRH)FDA Link
01/2002 - 07/2000
2Hormones (Hormone)IBA
11/2000 - 10/2000
16-chloro-2-(1-piperazinyl)pyrazine (CPP)IBA
01/2002
1Cytochrome P-450 CYP11B2 (CYP11B2)IBA
07/2001
1AldosteroneIBA
07/2001
1Hydrocortisone (Cortisol)FDA LinkGeneric
07/2001
1Steroid 11-beta-Hydroxylase (11 beta-Hydroxylase)IBA
07/2001
1SteroidsIBA
07/2001
1GlucocorticoidsIBA
01/2001
1Proteins (Proteins, Gene)FDA Link
11/2000