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ELISA Kit for Human Protein Wnt-7a

BHE13811954
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+1 866.986.9598
Email
[email protected]
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Uniprot O00755
Gene Name WNT7A
Immunogen Species Homo Sapiens (Human)
Kegg hsa:7476
Unigene Hs.72290
Reference
  1. 1.
    "Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25."
    Bui T.D., Lako M., Lejeune S., Curtis A.R.J., Strachan T., Lindsay S., Harris A.L.
    Gene189:25-29(1997) [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 [MRNA]
    tissue: Fetal brain.
  2. 2.
    "Isolation, characterization and chromosomal assignment of the human WNT7A gene."
    Ikegawa S., Kumano Y., Okui K., Fujiwara T., Takahashi E., Nakamura Y.
    Cytogenet. Cell Genet.74:149-152(1996) [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 [MRNA]
  3. 3.
    [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 GENOMIC DNA]
  4. 4.
    "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: Ovary.
  5. 5.
    "Differential expression of human Wnt genes 2, 3, 4, and 7B in human breast cell lines and normal and disease states of human breast tissue."
    Huguet E.L., McMahon J.A., McMahon A.P., Bicknell R., Harris A.L.
    Cancer Res.54:2615-2621(1994) [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 [MRNA] OF 204-327
    tissue: Mammary gland.
  6. 6.
    "Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome."
    Woods C.G., Stricker S., Seemann P., Stern R., Cox J., Sherridan E., Roberts E., Springell K., Scott S., Karbani G., Sharif S.M., Toomes C., Bond J., Kumar D., Al-Gazali L., Mundlos S.
    Am. J. Hum. Genet.79:402-408(2006) [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 FUHRS THR-109;VARIANT LPHAS CYS-292;CHARACTERIZATION OF VARIANT FUHRS THR-109;CHARACTERIZATION OF VARIANT LPHAS CYS-292
  7. 7.
    "Al-Awadi/Raas-Rothschild syndrome: two new cases and review."
    Lonardo F., Sabba G., Luquetti D.V., Monica M.D., Scarano G.
    Am. J. Med. Genet. A143:3169-3174(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: VARIANT LPHAS CYS-292
  8. 8.
    "A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome."
    Kantaputra P.N., Mundlos S., Sripathomsawat W.
    Am. J. Med. Genet. A152:2832-2837(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 LPHAS TRP-222
  9. 9.
    "Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation."
    Garavelli L., Wischmeijer A., Rosato S., Gelmini C., Reverberi S., Sassi S., Ferrari A., Mari F., Zabel B., Lausch E., Unger S., Superti-Furga A.
    Am. J. Med. Genet. A155:332-336(2011) [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 LPHAS LYS-72
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BHE13811954 E5407h 96T $736
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