Hanley, Neil A.
Neil A. Hanley
Hanley, Neil A., 1969-....
VIAF ID: 162332546 (Personal)
Permalink: http://viaf.org/viaf/162332546
Preferred Forms
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100 1 _ ‡a Hanley, Neil A
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100 1 _ ‡a Hanley, Neil A.
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100 1 _ ‡a Hanley, Neil A.
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100 1 _ ‡a Hanley, Neil A., ‡d 1969-....
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100 0 _ ‡a Neil A. Hanley
4xx's: Alternate Name Forms (2)
Works
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Age-specific changes in sex steroid biosynthesis and sex development |
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Analysis of SOX2 expression in developing human testis and germ cell neoplasia |
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Assessing the safety of stem cell therapeutics |
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Beta cell differentiation during early human pancreas development. |
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Biocompatibility and osteogenic potential of human fetal femur-derived cells on surface selective laser sintered scaffolds |
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Bone marrow-derived cells and the vasculature in diabetes: from biomarker to treatment? |
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Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731 |
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Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration |
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Chronological expression of Ciliated Bronchial Epithelium 1 during pulmonary development |
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Closing in on pancreatic beta cells |
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Commonalities in the endocrinology of stem cell biology and organ regeneration. |
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Cushing's syndrome in women with polycystic ovaries and hyperandrogenism |
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Derivation of a novel undifferentiated human foetal phenotype in serum-free cultures with BMP-2. |
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Development of the human pancreas from foregut to endocrine commitment. |
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The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal development. |
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Dynamic changes in the epigenomic landscape regulate human organogenesis and link to developmental disorders |
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The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture. |
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Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis |
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Embryonic stem cells to beta-cells by understanding pancreas development |
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Epimorphin alters the inhibitory effects of SOX9 on Mmp13 in activated hepatic stellate cells. |
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Essential endocrinology and diabetes |
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Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation |
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Generation of Distal Airway Epithelium from Multipotent Human Foregut Stem Cells |
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Genes, mice and the internet: is WT1 the shape of things to come? |
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Human embryo and early fetus research |
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Human embryonic germ cells for future neuronal replacement therapy |
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The human fetal adrenal cortex and the window of sexual differentiation |
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Human notochordal cell transcriptome unveils potential regulators of cell function in the developing intervertebral disc |
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Human pluripotent stem cells for modeling toxicity |
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Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes |
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Hypoxia inducible factors regulate pluripotency and proliferation in human embryonic stem cells cultured at reduced oxygen tensions |
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Identification of a primitive intestinal transcription factor network shared between esophageal adenocarcinoma and its precancerous precursor state |
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In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development |
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In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets |
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Inactivating PAPSS2 mutations in a patient with premature pubarche |
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Inactivation of Six2 in mouse identifies a novel genetic mechanism controlling development and growth of the cranial base |
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Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy |
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Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets. |
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An integrative transcriptomic atlas of organogenesis in human embryos |
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LRIG2 mutations cause urofacial syndrome |
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Maturation of induced pluripotent stem cell derived hepatocytes by 3D-culture |
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The methyltransferase WBSCR22/Merm1 enhances glucocorticoid receptor function and is regulated in lung inflammation and cancer |
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MicroRNA-122: a novel hepatocyte-enriched in vitro marker of drug-induced cellular toxicity. |
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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome |
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A novel immunomodulator, FTY-720 reverses existing cardiac hypertrophy and fibrosis from pressure overload by targeting NFAT (nuclear factor of activated T-cells) signaling and periostin |
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Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia. |
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Osteopontin is a novel downstream target of SOX9 with diagnostic implications for progression of liver fibrosis in humans |
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Periderm prevents pathological epithelial adhesions during embryogenesis. |
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Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease |
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Phenotypic and functional analyses show stem cell-derived hepatocyte-like cells better mimic fetal rather than adult hepatocytes. |
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Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment. |
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The self-orientation of mammalian cells in optical tweezers--the importance of the nucleus |
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SF-1: a critical mediator of steroidogenesis. |
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The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma. |
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SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development |
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Stem cell-derived hepatocytes as a predictive model for drug-induced liver injury: are we there yet? |
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Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease |
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Steroidogenic enzyme expression within the adrenal cortex during early human gestation |
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Steroidogenic factor 1 (SF-1) is essential for ovarian development and function |
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The stress of starvation: glucocorticoid restraint of beta cell development |
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Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes |
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Survival in a case of life-threatening flecainide overdose |
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TEAD and YAP regulate the enhancer network of human embryonic pancreatic progenitors |
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A tissue-specific, Gata6-driven transcriptional program instructs remodeling of the mature arterial tree |
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Tissue-specific knockouts of steroidogenic factor 1. |
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Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1 |
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Understanding the role of SOX9 in acquired diseases: lessons from development |
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Weighing up beta-cell mass in mice and humans: self-renewal, progenitors or stem cells? |
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The window period of NEUROGENIN3 during human gestation |
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Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3. |
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