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LHX1 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LIM Homeobox 1 试剂盒 (10) 和 LIM Homeobox 1 蛋白 (9)和数多这个蛋白质的别的产品。
Showing 10 out of 74 products:
Human Monoclonal LHX1 Primary Antibody for FACS, ICC - ABIN4330988
Xia, Nivet, Sancho-Martinez, Gallegos, Suzuki, Okamura, Wu, Dubova, Esteban, Montserrat, Campistol, Izpisua Belmonte: Directed differentiation of human pluripotent cells to ureteric bud kidney progenitor-like cells. in Nature cell biology 2013
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Cow (Bovine) Polyclonal LHX1 Primary Antibody for WB - ABIN2779598
Phillips: Assignment of LHX1 to human chromosome bands 17q11.2-->q12 by use of radiation hybrid mapping and somatic cell hybridization. in Cytogenetic and genome research 2002
Report novel missense mutation in LHX1 in congenital absence of the uterus and vagina which could change the transcriptional activity of LHX1 and its effect on the regulation of the downstream target gene GSC (显示 GSC 抗体).
Our MRKH families included 43 quads, 26 trios, and 30 duos. Of our MRKH probands, 87/147 (59%) had MRKH type 1 and 60/147 (41%) had type 2 with additional anomalies. CONCLUSION(S): Although the prevalence of WNT4 (显示 WNT4 抗体), HNF1B (显示 HNF1B 抗体), and LHX1 point mutations is low in people with MRKH, the prevalence of CNVs was approximately 19%.
Data have identified TBX6 (显示 TBX6 抗体) as a new gene associated with Mullerian aplasia. The results also support the relevance of LHX1 and CNVs in the development of this congenital malformation.
study concludes that heterozygous mutations of LHX1 might be one cause of the Mayer-Rokitansky-Kuster-Hauser syndrome in a subgroup of patients
Data indicate that expression of ERAS, LHX1, and CCRK (显示 CDK20 抗体) is increased in aggressive subgroups of medulloblastomas.
Lim1/LIM1 expression in neonatal, adult mouse and human endometrium suggesting Lim1/LIM1 may have a role in endometrial development and remodelling
Mutations in the coding regions of LHX1 may not be a common genetic etiologic factor involved in Han Chinese patients with mullerian duct abnormalities.
Eleven dysplastic kidneys showed no expression of LIM1. In contrast, 12 of 32 nephroblastomas showed nuclear positivity.
findings establish that the developmental marker Lim1 acts as an oncogene (显示 RAB1A 抗体) in cancer cells and targeting Lim1 may constitute an innovative therapeutic intervention in human lear cell carcinoma
Lim1 (also known as Lhx1) gene consists of a DNA-binding homeodomain and 2 cysteine-rich LIM (显示 PDLIM5 抗体) domains, which may participate in protein to protein interactions, and encodes a transcription factor.
Smad4 (显示 SMAD4 抗体)/Eomes (显示 EOMES 抗体)-dependent Lhx1 expression in the epiblast marks the entire definitive endoderm lineage, the anterior mesendoderm, and midline progenitors.
LHX1 is required in the anterior mesendoderm, but not in the mesoderm, for formation of the head.
Lhx1 maintains synchrony among circadian oscillator neurons of the suprachiasmatic nucleus.
Lhx1 is necessary for SCN (显示 SRI 抗体) terminal differentiation, including expression of neuropeptides profoundly important for circadian function.
OTX2 (显示 OTX2 抗体) has a role in regulating Dkk1 (显示 DKK1 抗体) and Lhx1 activity in the anterior mesendoderm
These studies identify LHX1 as the first transcription factor that is essential in the Mullerian duct epithelial progenitor cells for female reproductive tract development.
a core regulatory subcircuit composed of Pax2 (显示 PAX2 抗体)/8, Gata3 (显示 GATA3 抗体) and Lim1 turns on a deeper layer of transcriptional regulators while activating effector genes responsible for cell signaling and tissue organization.
Lhx1 therefore may influence the localization of primordial germ cells by modulating Ifitm1 (显示 IFITM1 抗体)-mediated repulsive activity.
The response of LMC motor neurons to Reelin (显示 RELN 抗体) is gated by Foxp1 (显示 FOXP1 抗体)- and Lhx1-mediated regulation of expression of the critical Reelin (显示 RELN 抗体) signalling intermediate Dab1 (显示 DAB1 抗体).
Inactivation of either PINCH isoform independently leads to instability of ILK, loss of stretch-responsive anf and vegf expression, and progressive heart failure
These results demonstrate an essential role for Lhx1 in driving specification of the entire kidney field from the intermediate mesoderm.
nephrogenic transcription factors (osr1 (显示 OSR1 抗体), osr2, hnf1b (显示 HNF1B 抗体), lhx1, pax8 (显示 PAX8 抗体))play important role in nephrogenesis but have no pronephros induction potential upon overexpression; they activate transcription cascades reflecting activation by activin A (显示 INHBA 抗体), retinoic acid
Substantial evidence is found for a prosomeric organization of the diencephalon based on alternating expression of Lhx1/5 and Lhx2 (显示 LHX2 抗体)/9 genes during larval development and in the adult.
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 important for the development of the renal and urogenital systems. This gene is a candidate for Mayer-Rokitansky-Kuster-Hauser syndrome, a disorder characterized by anomalies in the female genital tract.
LIM homeobox protein 1
, LIM/homeobox protein Lhx1
, homeobox protein Lim-1
, LIM homeo box protein 1
, domesticus (clone 2.3 kB) lim-1
, Homeobox protein LMX-2
, Homeobox protein Lim-1