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LHX4 encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. 再加上，我们可以发LHX4 试剂盒 (10) 和 LHX4 蛋白 (4)和数多这个蛋白质的别的产品。
Showing 10 out of 66 products:
Human Polyclonal LHX4 Primary Antibody for WB - ABIN1881496
Castinetti, Saveanu, Reynaud, Quentien, Buffin, Brauner, Kaffel, Albarel, Guedj, El Kholy, Amin, Enjalbert, Barlier, Brue: A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism. in The Journal of clinical endocrinology and metabolism 2008
Show all 4 Pubmed References
Human Polyclonal LHX4 Primary Antibody for IF, WB - ABIN529948
Hung, Hu, Ho, Chiu, Lee, Jeng, Shih, Lee: Downregulation of alpha-fetoprotein expression by LHX4: a critical role in hepatocarcinogenesis. in Carcinogenesis 2011
Lhx3 (显示 LHX3 抗体) and Lhx4 have roles in suppressing Kolmer-Agduhr interneuron characteristics within zebrafish axial motoneurons
LHX4 Mutation is associated with Pituitary Deficits.
The study identified 4 new LHX4 heterozygous allelic variants in patients with congenital hypopituitarism: W204X, delK242, N271S and Q346R.
A novel homozygous mutation in LHX4 associated with a lethal phenotype, implying that recessive mutations in LHX4 may be incompatible with life.
we found that LHX4 upregulated beta-catenin (显示 CTNNB1 抗体) levels in human colorectal cancer cell lines
Data indicate that HESX1 (显示 HESX1 抗体), LHX4 and SOX3 (显示 SOX3 抗体) polymorphisms may be associated with pituitary stalk interruption syndrome (PSIS).
This study is the first to describe, a gradual loss of ACTH (显示 POMC 抗体) in a patient carrying an LHX4 mutation.
Variably penetrant pituitary insufficiency, including this severe and atypical presentation, can be correlated with LHX4 insufficiency and highlights the role of LHX4 for pituitary development.
data indicate that LHX4 may act as a potential tumor suppressor in hepatocarcinogenesis, suggesting that targeting LHX4 to downregulate AFP (显示 AFP 抗体) might have therapeutic implications
A novel HESX1 (显示 HESX1 抗体) causative mutation was found in a consanguineous family, and two LHX4 mutations were present in familial Pituitary stalk interruption syndrome.
"Heterozygous splice site mutations within LHX4 are associated with combined pituitary hormone deficiency and isolated growth hormone deficiency... small sella turcica...persistent craniopharyngeal canal...ectopic posterior pituitary... " P. 207
some polymorphisms in LHX4 are associated with growth traits at certain ages, and may be used as candidates for marker-assisted selection and management
conditional deletion of Shh (显示 SHH 抗体) in the anterior hypothalamus results in a fully penetrant phenotype characterised by a complete arrest of (Rathke's pouch) RP development, with lack of Lhx3 (显示 LHX3 抗体)/Lhx4 expression in RP epithelium.
We discovered that expression of Cdkn1a (显示 CDKN1A 抗体) is expanded dorsally in the pituitary primordium of both Lhx3 (显示 LHX3 抗体) and Lhx4 mutants. Lhx4 mutants exhibit reduced cyclin D1 (显示 CCND1 抗体) expression and have auxiliary pouch-like structures.
X-ray crystal- and small-angle x-ray scattering-derived solution structures of an Lhx4.Isl2 (显示 ISL2 抗体) complex exhibit many similarities with that of Lhx3 (显示 LHX3 抗体).Isl1 (显示 ISL1 抗体); structural differences supported by mutagenic studies reveal differences in the mechanisms of binding.
Lhx4 and Prop1 (显示 PROP1 抗体) have critical, but mechanistically different roles in specification and expansion of specialized anterior pituitary cells
We conclude Sp1 (显示 SP1 抗体) directly regulates Lhx4 gene expression.
Results show that Lhx3 (显示 LHX3 抗体) exhibits specific spatial and temporal expression in the mouse placenta, but that absence of both LHX3 (显示 LHX3 抗体) and 4 genes did not interfere with placental transport nor consistently with expression of target genes such as Gnrhr (显示 GNRHR 抗体).
Successful purification and crystallization of an engineered complex comprising the LIM (显示 PDLIM5 抗体) domains of motor neuron protein Lhx4 and the Lim (显示 PDLIM5 抗体) binding domain of Isl2 (islet 2 (显示 ISL2 抗体) protein) are reported.
This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor involved in the control of differentiation and development of the pituitary gland. Mutations in this gene cause combined pituitary hormone deficiency 4.
LIM homeobox 4
, LIM homeobox protein 4
, LIM/homeobox protein Lhx4
, LIM/homeobox protein Lhx4-like
, LIM homeo box protein 4