(Q37955972)

25 August 2017

title

Transcription factors in parathyroid development: lessons from hypoparathyroid disorders (English)

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25 August 2017

2

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25 August 2017

Irina V Grigorieva

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25 August 2017

language of work or name

English

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publication date

1 November 2011

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Annals of the New York Academy of Sciences

25 August 2017

number of pages

15

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based on heuristic

inferred from page(s)

published in

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25 August 2017

volume

1237

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25 August 2017

page(s)

24-38

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The origin of the parathyroid gland

25 August 2017

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21 January 2018

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The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis

21 January 2018

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Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

21 January 2018

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Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion

21 January 2018

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Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development

21 January 2018

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Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia

21 January 2018

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GATA3 haplo-insufficiency causes human HDR syndrome

21 January 2018

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Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

21 January 2018

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Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.

21 January 2018

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Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factor.

21 January 2018

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A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome

21 January 2018

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FOG, a multitype zinc finger protein, acts as a cofactor for transcription factor GATA-1 in erythroid and megakaryocytic differentiation

21 January 2018

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Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

21 January 2018

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Hearing loss following Gata3 haploinsufficiency is caused by cochlear disorder

21 January 2018

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GATA3 haploinsufficiency causes a rapid deterioration of distortion product otoacoustic emissions (DPOAEs) in mice.

21 January 2018

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Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2

21 January 2018

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Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system

21 January 2018

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Pax 2/8-regulated Gata 3 expression is necessary for morphogenesis and guidance of the nephric duct in the developing kidney

21 January 2018

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Gata3 acts downstream of beta-catenin signaling to prevent ectopic metanephric kidney induction

21 January 2018

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Genetic ablation of parathyroid glands reveals another source of parathyroid hormone

21 January 2018

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Thymus-associated parathyroid hormone has two cellular origins with distinct endocrine and immunological functions.

21 January 2018

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Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis

21 January 2018

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Calcium-sensing receptor expression is regulated by glial cells missing-2 in human parathyroid cells

21 January 2018

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Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism

21 January 2018

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Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.

21 January 2018

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Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism

21 January 2018

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Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidism.

21 January 2018

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Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism.

21 January 2018

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A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism.

21 January 2018

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Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies

21 January 2018

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An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

21 January 2018

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Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

21 January 2018

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SOX3 is required during the formation of the hypothalamo-pituitary axis

21 January 2018

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Long-range control of gene expression: emerging mechanisms and disruption in disease

21 January 2018

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Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients.

21 January 2018

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21 January 2018

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An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21

21 January 2018

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21 January 2018

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21 January 2018

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Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins

21 January 2018

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A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients.

21 January 2018

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Mutations in the AIRE gene: effects on subcellular location and transactivation function of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy protein

21 January 2018

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Aire regulates negative selection of organ-specific T cells

21 January 2018

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Anti-interferon autoantibodies in autoimmune polyendocrinopathy syndrome type 1

21 January 2018

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Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen

21 January 2018

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Crucial role for the Nalp3 inflammasome in the immunostimulatory properties of aluminium adjuvants

21 January 2018

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Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotype

21 January 2018

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Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5

21 January 2018

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The role of Hoxa3 gene in parathyroid gland organogenesis of the mouse

21 January 2018

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Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs

21 January 2018

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undulated phenotypes suggest a role of Pax-1 for the development of vertebral and extravertebral structures.

21 January 2018

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Characterization and developmental expression of Pax9, a paired-box-containing gene related to Pax1

21 January 2018

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Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

21 January 2018

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Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1

21 January 2018

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Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development

21 January 2018

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Getting your Pax straight: Pax proteins in development and disease

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Pax genes and organogenesis: Pax9 meets tooth development.

21 January 2018

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Increased thymus- and decreased parathyroid-fated organ domains in Splotch mutant embryos

21 January 2018

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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida

21 January 2018

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Mutations in PAX3 associated with Waardenburg syndrome type I.

21 January 2018

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The eyes absent gene: genetic control of cell survival and differentiation in the developing Drosophila eye.

21 January 2018

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A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

21 January 2018

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Renal failure and deafness: branchio-oto-renal syndrome.

21 January 2018

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Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome

21 January 2018

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Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

21 January 2018

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Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya

21 January 2018

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Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome

21 January 2018

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SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

21 January 2018

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Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

21 January 2018

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GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1749-6632.2011.06221.X

Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1

21 January 2018

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Congenital heart disease in mice deficient for the DiGeorge syndrome region

21 January 2018

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10.1111/J.1749-6632.2011.06221.X

21 January 2018

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DOI

1 reference

25 August 2017

1 reference