GPI-anchored small leucine-rich proteoglycan gene NYX

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Recombinant dna technique included in method of making a...

Reexamination Certificate

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C435S320100, C536S023100, C536S023500, C530S350000

Reexamination Certificate

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06875585

ABSTRACT:
A mammalian gene (NYX) which encodes a GPI-anchored small leucine-rich proteoglycan, nyctalopin, together with compositions and methods involving NYX and nyctalopin or homologous molecules. Mutations in NYX may cause complete X-linked congenital stationary night blindness in humans.

REFERENCES:
Yan et al., 2000, Science, 290, pp. 523-527.*
Introduction to proteins and protein engineering, 1986, Elsevier, p. 41.*
Loss of Function Mutations in a Calcium-Channelα1subunit gene in Xp11.23 cause incomplete X-linked congenital stationary Night blindness—Paper by Bach-Hansen, et al. Jul., 1996.
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked incomplete cogenital stationary night blindness—Paper by Bech-Hansen et al. Nov., 2000.
Evidence for Genetic Heterogeneity in X-linked Cogenital Stationary Night Blindness—Paper by Bech-Hansen, et al.—published Apr. 7, 1998.
Leucine-Rich Repeat Glycoproteins of the Extracellular Matrix—Paper by Hocking, et al. accepted Jan. 29, 1998.

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