anti-Insulinoma-Associated 1 (INSM1) Anticorps

Human Insulinoma-Associated 1 (INSM1) interaction partners

1. Our data suggest that children with the INSM1 binding site within the CLDN14 (Montrer CLDN14 Anticorps) risk haplotype have a higher likelihood of hypercalciuria and kidney stones. Enhanced CLDN14 (Montrer CLDN14 Anticorps) expression may play a role in the pathophysiology of their hypercalciuria.

2. High INSM1 expression is associated with small-cell lung cancer.

3. Suggest that INSM1 is valuable for identification of the high-grade thoracic neuroendocrine carcinomas that are sometimes negative for synaptophysin (Montrer SYP Anticorps), chromogranin, and CD56 (Montrer NCAM1 Anticorps).

4. Solution NMR structure of zinc finger 4 (Montrer YIPF4 Anticorps) and 5 from human INSM1 has been presented.

5. INSM1 is closely related to the development of high-grade neuroendocrine carcinoma of uterine cervix, and a useful new neuroendocrine marker in conducting its correct and rapid diagnosis

6. Data supports our hypothesis that a positive-feedback loop of sonic hedgehog (Montrer SHH Anticorps) signaling induced INSM1 through N-myc (Montrer MYCN Anticorps) and INSM1 enhanced N-myc (Montrer MYCN Anticorps) stability contributing to the transformation of human neuroblastoma (Montrer ARHGEF16 Anticorps).

7. Small cell lung cancer tissues were strongly positive for INSM1. INSM1 signal was not detected on normal adjacent tissues from lung cancer patients or normal lung tissues

8. the INSM1-promoter specific conditional replicating adenovirus represents a sensitive diagnostic tool to aid clinicians in the detection of NE tumors.

9. Insulinoma-Associated Protein 1 is a crucial regulator of neuroendocrine differentiation in lung cancer.

10. INSM1 autoantibodies were associated with risk of developing type 1 diabetes.

Mouse (Murine) Insulinoma-Associated 1 (INSM1) interaction partners

1. An INSM1/RCOR1 (Montrer Rcor2 Anticorps)/2 complex controls the balance of proliferation and differentiation during brain development.

2. INSM1 ectopic expression impairs normal lung development especially in postnatal alveologenesis.

3. Insm1 is the earliest known gene expressed in outer versus inner hair cells, demonstrating that nascent outer hair cells initiate a unique differentiation program in the embryo, much earlier than previously believed.

4. Insm1-dependent Hes1 (Montrer HES1 Anticorps) repression is required for neuroendocrine development.

5. INSM1 interacts with RACK1 (Montrer GNB2L1 Anticorps) protein and facilitates insulin receptor (Montrer INSR Anticorps) -mediated signaling.

6. Insm1 works to promote endocrine cell differentiation in a pathway that involves Neurog3 and Ripply3

7. Data suggest that IA-2 (Montrer PTPRN Anticorps) and IA-2beta (Montrer PTPRN2 Anticorps) play important roles in regulation of circadian rhythm, likely through neurochemical communication among neurons of suprachiasmatic nucleus. [Insm2 (Montrer INSM2 Anticorps)-beta; IA-2beta (Montrer PTPRN2 Anticorps); insulinoma-associated protein 2 (Montrer INSM2 Anticorps)-beta]

8. Insm1 acts in the epigenetic and transcriptional network that controls differentiation of endocrine cells in the anterior pituitary gland, and that it requires the SNAG domain to exert this function in vivo.

9. This study suggested that Insm1 in promoting the transition of progenitors from apical and proliferative to basal, terminal and neuronogenic.

10. isolation, characterization, and identification of an interacting protein, Cbl (Montrer CBL Anticorps)-associated protein (CAP)

Zebrafish Insulinoma-Associated 1 (INSM1) interaction partners

1. characterization of two zebrafish Insm1-like genes, insm1a and insm1b, and analysis of their expression patterns during embryonic development

Xenopus laevis Insulinoma-Associated 1 (INSM1) interaction partners

1. insm1 is expressed in regions of the tadpole brain and retina harboring populations of progenitor cells.

2. results reveal that IA1 constitutes a novel player downstream of Xash1 (Montrer ASCL1 Anticorps) in the formation of a previously unidentified population of Xenopus noradrenergic primary neurons