ALX Homeobox 4 (ALX4) ELISA Kits

ALX4 encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue. Zusätzlich bieten wir Ihnen ALX4 Antikörper (58) und ALX4 Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
Anti-Human ALX4 ALX4 60529 Q9H161
Anti-Ratte ALX4 ALX4 296511  
Anti-Maus ALX4 ALX4 11695 O35137
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Weitere ELISA Kits für ALX4 Interaktionspartner

Human ALX Homeobox 4 (ALX4) Interaktionspartner

  1. overexpression of ALX4 inhibited the proliferation, invasion, and epithelial-mesenchymal transition (EMT (zeige ITK ELISA Kits)) in HCC (zeige FAM126A ELISA Kits) cells. ALX4 had an inhibitory effect on the sonic hedgehog (Shh (zeige SHH ELISA Kits)) 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 (zeige HOXB13 ELISA Kits)/SLUG and ALX4/SLUG axes are novel pathways that promote EMT (zeige ITK ELISA Kits) and invasion of ovarian cancer cells.

  4. High-quality solution NMR structures of three homeodomains from human proteins ALX4, ZHX1 (zeige ZHX1 ELISA Kits) and CASP8AP2 (zeige CASP8AP2 ELISA Kits) 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 (zeige HOXB2 ELISA Kits), HoxB4 (zeige HOXB4 ELISA Kits) 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) Interaktionspartner

Mouse (Murine) ALX Homeobox 4 (ALX4) Interaktionspartner

  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 (zeige PTPN11 ELISA Kits)-FGF signaling in the neural crest for lacrimal gland development.

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

  3. Alx4 genetically interacts with and Shh (zeige SHH ELISA Kits) and Gli3 (zeige GLI3 ELISA Kits) 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 (zeige FOXC1 ELISA Kits) regulation of Msx2 and Alx4.

  6. the loss of the severe preaxial polydactyly characteristic of Gli3 (zeige GLI3 ELISA Kits)-/- 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 (zeige GLI3 ELISA Kits) and Shh (zeige SHH ELISA Kits).

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

ALX4 Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit ALX Homeobox 4 (ALX4) ELISA Kits

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

Bezeichner auf Proteinebene für ALX Homeobox 4 (ALX4) ELISA Kits

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 SPEZIES
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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