Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid
Reexamination Certificate
2006-05-09
2006-05-09
Myers, Carla J. (Department: 1634)
Chemistry: molecular biology and microbiology
Measuring or testing process involving enzymes or...
Involving nucleic acid
C435S091100, C435S091200, C536S023100, C536S023500, C536S024310, C536S024330
Reexamination Certificate
active
07041450
ABSTRACT:
The present invention relates to a method and kit for diagnosing GH (growth hormone) deficiency, in particular isolated growth hormone deficiency II (IGHD II). The method comprises the steps of analysing the missense mutation G6191to T in exon 4 of GH-1 which changes valine 110 to phenylalanine.
REFERENCES:
Lucentini, J. The Scientist. Dec. 2004, p. 20.
Wajnrajach et al,Pathophysiology of Autosomal Dominant GH Deficiency,Programs and Abstracts from the 79th Annual Meeting of The Endocrine Society, Minneapolis, MN, Abstract PI-84, p. 155 (1997).
Pfäffle et al,Horm. Res.,53(Suppl 3):1-8(2000).
Phillips et al,Proc. Natl. Acad. Sci. USA,78:6372-6375 (1981).
Wajnarajch et al,Nature Genetics,12:88-90 (1996).
Cogan et al,Journal of Clinical Endocrinology and Metabolism,76(5):1224-1228 (1993).
Binder et al,Journal of Clinical Endocrinology and Metabolism,80(4):1247-1252 (1995).
Wagner et al,Pediatric Research,43(1):105-110 (1998).
Binder et al,Journal of Clinical Endocrinology and Metabolism,81(11): 4047-4050 (1996).
Hayashi et al,Journal of Clinical Endocrinology and Metabolism,84(6):2134-2139 (1999).
Lee et al,Endocrinology,14(3):883-890 (2000).
Cogan et al,Journal of Clinical Endocrinology and Metabolism,80(12):3591-3595 (1995).
Cogan et al,Human Molecular Genetics,6(6):909-912 (1997).
Missarelli et al,Human Genetics,101:113-117 (1997).
Hayashi et al,Growth Hormone and IGF Research,9:434-437 (1999).
McCarthy et al,Human Molecular Genetics,7(9):1491-1496 (1998).
Duquesnov et al,Familial isolated growth hormone deficiency with slight height reduction due to a heterozygote mutation in GH gene,(Abstract), Proc. 80th Meeting of The Endocrine Society, P2-202 (1998).
Massa et al,Eur. J. Pediatr.,157:272-275 (1998).
Blum et al,Journal of Clinical Endocrinology and Metabolism,76(6): 1610-1616 (1993).
Chomczynski et al,Analytical Biochemistry,162:156-159 (1987).
Chen et al,Genomics,4:479-797 (1989).
Watakabe et al,Genes&Development,7:407-418 (1993).
Prader et al,Helv. Paediat. Acta.(Suppl.), 43:3-125 (1998).
Argyropoulou et al,Pediatric Radiologyi,21:247-249 (1991).
Danies,Vitamins and Hormones,58:1-26 (2000).
Cooper et al,The Metabolic and Molecular Bases of Inherited Disease,7th Edition, New York: McGraw-Hill, pp. 259-291, undated.
Ultsch et al,J. Med. Biol.,236:286-299 (1994).
Woods et al,Balliere's Clinical Endocrinology and Metabolism,10(3):371-383 (1996).
Murray et al,Am. J. Neuroadiol.,21:685-689 (2000).
Thorner et al,Williarn's Textbook of Endocrinology,9:249-340 (1998).
Hamilton et al,Am. J. Neuroadiol.,19:1609-1615 (1998).
Zucchini et al,Journal of Pediatric Endocrinology&Metabolism,9:545-548 (1996).
Dinsmore & Shohl LLP
Myers Carla J.
Pharmacia AB
LandOfFree
Method for diagnosing GH deficiency does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Method for diagnosing GH deficiency, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method for diagnosing GH deficiency will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3640475