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ELISA Kit for Human Noggin

BHE13808281
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Uniprot Q13253
Gene Name NOG
Immunogen Species Homo Sapiens (Human)
Kegg hsa:9241
Unigene Hs.248201
Reference
  1. 1.
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]
    tissue: Placenta.
    tissue: Temporal cortex.
  2. 2.
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res.14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]
    tissue: Prostate.
  3. 3.
    "Structural basis of BMP signalling inhibition by the cystine knot protein Noggin."
    Groppe J., Greenwald J., Wiater E., Rodriguez-Leon J., Economides A.N., Kwiatkowski W., Affolter M., Vale W.W., Belmonte J.C., Choe S.
    Nature420:636-642(2002) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: X-RAY CRYSTALLOGRAPHY (2.42 ANGSTROMS) OF 28-232 IN COMPLEX WITH BMP7;FUNCTION;SUBUNIT;DISULFIDE BONDS
  4. 4.
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS SYM1A ARG-35; CYS-189; ASN-220; CYS-222; ASP-222 AND LEU-223;VARIANT SYNS1 GLY-217
  5. 5.
    "Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome."
    Takahashi T., Takahashi I., Komatsu M., Sawaishi Y., Higashi K., Nishimura G., Saito H., Takada G.
    Clin. Genet.60:447-451(2001) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT SYM1A TYR-184
  6. 6.
    "Identical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangism."
    Dixon M.E., Armstrong P., Stevens D.B., Bamshad M.
    Genet. Med.3:349-353(2001) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS TCC ARG-35; LEU-204 AND CYS-222
  7. 7.
    "Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin."
    Brown D.J., Kim T.B., Petty E.M., Downs C.A., Martin D.M., Strouse P.J., Moroi S.E., Milunsky J.M., Lesperance M.M.
    Am. J. Hum. Genet.71:618-624(2002) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: INVOLVEMENT IN SABTS
  8. 8.
    "Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism."
    Mangino M., Flex E., Digilio M.C., Giannotti A., Dallapiccola B.
    Hum. Mutat.19:308-308(2002) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT SYM1A SER-35
  9. 9.
    "The facio-audio-symphalangism syndrome in a four generation family with a nonsense mutation in the NOG-gene."
    van den Ende J.J., Mattelaer P., Declau F., Vanhoenacker F., Claes J., Van Hul E., Baten E.
    Clin. Dysmorphol.14:73-80(2005) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT SYM1A CYS-205
  10. 10.
    "A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN."
    Lehmann K., Seemann P., Silan F., Goecke T.O., Irgang S., Kjaer K.W., Kjaergaard S., Mahoney M.J., Morlot S., Reissner C., Kerr B., Wilkie A.O.M., Mundlos S.
    Am. J. Hum. Genet.81:388-396(2007) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANTS BDB2 ALA-35; SER-35; PRO-36; LYS-48; GLY-167 AND SER-187
  11. 11.
    "Facioaudiosymphalangism syndrome and growth acceleration associated with a heterozygous NOG mutation."
    Rudnik-Schoneborn S., Takahashi T., Busse S., Schmidt T., Senderek J., Eggermann T., Zerres K.
    Am. J. Med. Genet. A152:1540-1544(2010) [PubMed] [Europe PMC] [Abstract]
    [15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s) Cited for: VARIANT SYNS1 TRP-232
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BHE13808281 E0796h 96T $736
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