ALX Homeobox 4 (ALX4) Kits ELISA

ALX4 encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. De plus, nous expédions ALX4 Anticorps (59) et ALX4 Protéines (3) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
Anti-Humain ALX4 ALX4 60529 Q9H161
Anti-Rat ALX4 ALX4 296511  
Anti-Souris ALX4 ALX4 11695 O35137
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Plus Kits ELISA pour ALX4 partenaires d'interaction

Human ALX Homeobox 4 (ALX4) interaction partners

  1. overexpression of ALX4 inhibited the proliferation, invasion, and epithelial-mesenchymal transition (EMT (Montrer ITK Kits ELISA)) in HCC (Montrer FAM126A Kits ELISA) cells. ALX4 had an inhibitory effect on the sonic hedgehog (Shh (Montrer SHH Kits ELISA)) signaling pathway.

  2. mother of Case 2 also had a mutation in the ALX4 gene, but no enlarged parietal foramina

  3. Our results show that HOXB13 (Montrer HOXB13 Kits ELISA)/SLUG and ALX4/SLUG axes are novel pathways that promote EMT (Montrer ITK Kits ELISA) and invasion of ovarian cancer cells.

  4. High-quality solution NMR structures of three homeodomains from human proteins ALX4, ZHX1 (Montrer ZHX1 Kits ELISA) and CASP8AP2 (Montrer CASP8AP2 Kits ELISA) were solved.

  5. We suggest that all ALX4 heterozygote carriers be examined in detail for possible changes in nasal configuration, to establish a detailed genotype-phenotype correlation, leading the way to more comprehensive genetic counseling.

  6. Epigenetic silencing of Aristaless-like homeobox-4 is associated with lung cancer.

  7. study describes 2 related individuals with a heterozygous mutation in ALX4 presenting a distinct phenotype of frontonasal dysplasia; suggest that the loss of the ALX4 OAR domain with the maintenance of the homeodomain impairs the function of the normal allele in a dominant-negative effect

  8. ALX4 variants may have an impact on the genetic etiology of nonsyndromic craniosynostosis.

  9. Exclusion of mutations in ALX4 gene in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

  10. Downregulation of HoxB2 (Montrer HOXB2 Kits ELISA), HoxB4 (Montrer HOXB4 Kits ELISA) and Alx4 expression during the narrow window of early embryogenesis may cause omphalocele in the Cd chick model by interfering with molecular signaling required for proper VBW formation.

Cow (Bovine) ALX Homeobox 4 (ALX4) interaction partners

Mouse (Murine) ALX Homeobox 4 (ALX4) interaction partners

  1. Inactivation of ALX4/Alx4 causes lacrimal gland aplasia in both human and mouse. These results reveal a key role of Alx4 in mediating FGF-Shp2 (Montrer PTPN11 Kits ELISA)-FGF signaling in the neural crest for lacrimal gland development.

  2. novel allele of Alx4 results in reduced Fgf10 (Montrer FGF10 Kits ELISA) expression and failure of eyelid fusion in mice

  3. Alx4 genetically interacts with and Shh (Montrer SHH Kits ELISA) and Gli3 (Montrer GLI3 Kits ELISA) during genital tubercle formation.

  4. A mutagenesis study characterizes a polydactylous phenotype that is caused by a nonsense mutation in the Alx4 gene.

  5. Progression of calvarial bone development requires Foxc1 (Montrer FOXC1 Kits ELISA) regulation of Msx2 and Alx4.

  6. the loss of the severe preaxial polydactyly characteristic of Gli3 (Montrer GLI3 Kits ELISA)-/- limbs in double mutant embryos establishes that this type of polydactyly requires Alx4 function.

  7. Function and regulation of Alx4 in limb development entail complex genetic interactions with Gli3 (Montrer GLI3 Kits ELISA) and Shh (Montrer SHH Kits ELISA).

  8. Alx4, is required for normal branching morphogenesis of the ductal epithelia during pubescent mammary gland development.

ALX4 profil antigène

Antigen Summary

This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Mutations in this gene cause parietal foramina 2 (PFM2)\; an autosomal dominant disease characterized by deficient ossification of the parietal bones. Mutations in this gene also cause a form of frontonasal dysplasia with alopecia and hypogonadism\; suggesting a role for this gene in craniofacial development, mesenchymal-epithelial communication, and hair follicle development. Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS)\; a syndrome characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males. In mouse, this gene has been shown to use dual translation initiation sites located 16 codons apart.

Gene names and symbols associated with ALX Homeobox 4 (ALX4) Kits ELISA

  • ALX homeobox 4b (alx4b) anticorps
  • ALX homeobox 4a (alx4a) anticorps
  • ALX homeobox 4 (ALX4) anticorps
  • ALX homeobox 4 (Alx4) anticorps
  • aristaless-like homeobox 4 (Alx4) anticorps
  • alx4 anticorps
  • FND2 anticorps
  • im:7142878 anticorps
  • lst anticorps
  • zgc:162606 anticorps

Protein level used designations for ALX Homeobox 4 (ALX4) Kits ELISA

aristaless-like homeobox 4 , homeobox protein aristaless-like 4 , homeodomain transcription factor ALX4 , aristaless 4 , ALX-4 , Aristaless-like 4 , Strong's luxoid

GENE ID SPECIES
497424 Danio rerio
100006399 Danio rerio
60529 Homo sapiens
609979 Canis lupus familiaris
296511 Rattus norvegicus
594846 Bos taurus
373976 Gallus gallus
11695 Mus musculus
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