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ArticlesPeer ReviewedFull Text
Initial screening of the rs104893657 variant of the PAX8 gene in women with hypothyroidism from Northeastern Slovakia
Author / Creator:Mydlárová Blaščáková, Marta ; Homjáková, Barbora ; Nagy, Melinda ; Poráčová, Janka ; Lörinczová, Zuzana ; Makovický, Pavol ; Kimáková, Tatiana ; Sedlák, Vincent ; Konečná, Mária
Publisher:Czech Republic: National Institute of Public Health
Journal title:Central European journal of public health, 2023-12, Vol.31 (Suppl 1), p.S89-S94
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Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant
Author / Creator:Perone, Denise ; Medeiros-Neto, Geraldo ; Nogueira, Célia Regina ; Chagas, Antonio José ; Alves Dias, Vera Maria ; Viana, Maria Fátima ; Kopp, Peter
Publisher:Germany: De Gruyter
Journal title:Journal of Pediatric Endocrinology & Metabolism, 2016-02, Vol.29 (2), p.193-201
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Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands
Author / Creator:Kumorowicz-Czoch, Malgorzata ; Madetko-Talowska, Anna ; Dudek, Adam ; Tylek-Lemanska, Dorota
Publisher:Germany: De Gruyter
Journal title:Journal of Pediatric Endocrinology & Metabolism, 2015-07, Vol.28 (7), p.735-743
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Comparative genomics reveals a functional thyroid-specific element in the far upstream region of the PAX8 gene
Author / Creator:Nitsch, Roberto ; Di Dato, Valeria ; di Gennaro, Alessandra ; de Cristofaro, Tiziana ; Abbondante, Serena ; De Felice, Mario ; Zannini, Mariastella ; Di Lauro, Roberto
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2010-05, Vol.11 (1), p.306-306, Article 306
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Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism
Author / Creator:Vincenzi, Monica ; Camilot, Marta ; Ferrarini, Eleonora ; Teofoli, Francesca ; Venturi, Giacomo ; Gaudino, Rossella ; Cavarzere, Paolo ; De Marco, Giuseppina ; Agretti, Patrizia ; Dimida, Antonio ; Tonacchera, Massimo ; Boner, Attilio ; Antoniazzi, Franco
Publisher:England: BioMed Central Ltd
Journal title:BMC endocrine disorders, 2014-08, Vol.14 (1), p.69-69, Article 69
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Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect
Author / Creator:Jo, Wakako ; Ishizu, Katsura ; Fujieda, Kenji ; Tajima, Toshihiro
Publisher:Cairo, Egypt: Hindawi Limiteds
Journal title:Journal of Thyroid Research, 2010-01, Vol.2010 (2010), p.45-47
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Recovery of NIS expression in thyroid cancer cells by overexpression of Pax8 gene
Author / Creator:Presta, Ivan ; Arturi, Franco ; Ferretti, Elisabetta ; Mattei, Tiziana ; Scarpelli, Daniela ; Tosi, Emanuele ; Scipioni, Angela ; Celano, Marilena ; Gulino, Alberto ; Filetti, Sebastiano ; Russo, Diego
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2005-07, Vol.5 (1), p.80-80, Article 80
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Thyroid hormone receptor α1: a novel regulator of thyroid cancer cell differentiation
Author / Creator:Hwang, Eunmi ; Doolittle, Woo Kyung Lee ; Zhu, Yuelin Jack ; Zhu, Xuguang ; Zhao, Li ; Yu, Yanlin ; Cheng, Sheue-yann
Publisher:London: Nature Publishing Group UK
Journal title:Oncogene, 2023-10, Vol.42 (41), p.3075-3086
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Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank
Author / Creator:Foo, Heidi ; Thalamuthu, Anbupalam ; Jiang, Jiyang ; Koch, Forrest C. ; Mather, Karen A. ; Wen, Wei ; Sachdev, Perminder S.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2021-07, Vol.11 (1), p.14633-14633, Article 14633
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ArticlesPeer ReviewedFull Text
PAX8 regulon in human ovarian cancer links lineage dependency with epigenetic vulnerability to HDAC inhibitors
Author / Creator:Shi, Kaixuan ; Yin, Xia ; Cai, Mei-Chun ; Yan, Ying ; Jia, Chenqiang ; Ma, Pengfei ; Zhang, Shengzhe ; Zhang, Zhenfeng ; Gu, Zhenyu ; Zhang, Meiying ; Di, Wen ; Zhuang, Guanglei
Publisher:England: eLife Science Publications, Ltd
Journal title:eLife, 2019-05, Vol.8
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ArticlesPeer ReviewedFull Text
PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3
Author / Creator:Soriano, Amata Amy ; de Cristofaro, Tiziana ; Di Palma, Tina ; Dotolo, Serena ; Gokulnath, Priyanka ; Izzo, Antonella ; Calì, Gaetano ; Facchiano, Angelo ; Zannini, Mariastella
Publisher:England: BioMed Central
Journal title:Cancer cell international, 2019-11, Vol.19 (1), p.303-303, Article 303
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ArticlesPeer ReviewedFull Text
Genetic variant in CACNA1C is associated with PTSD in traumatized police officers
Author / Creator:Krzyzewska, Izabela M ; Ensink, Judith B M ; Nawijn, Laura ; Mul, Adri N ; Koch, Saskia B ; Venema, Andrea ; Shankar, Vinod ; Frijling, Jessie L ; Veltman, Dirk J ; Lindauer, Ramon J L ; Olff, Miranda ; Mannens, Marcel M A M ; van Zuiden, Mirjam ; Henneman, Peter
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2018-02, Vol.26 (2), p.247-257
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New Findings from Johannes Gutenberg-University in Clinical Endocrinology and Diabetes Provides New Insights (Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid Synd...
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2018-03, p.4308
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Newsletter articlesFull Text
Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affecte...
Publisher:NewsRX LLC
Journal title:Pediatrics Week, 2016, p.325
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Screening for Pax8 Mutations in Patients with Congenital Hypothyroidism in South-West Germany
Author / Creator:Lanzerath, Kirsten ; Bettendorf, Markus ; Haag, Christine ; Kneppo, Caroline ; Schulze, Egbert ; Grulich-Henn, Jürgen
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Hormone research in paediatrics, 2006-01, Vol.66 (2), p.96-100
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Newsletter articlesFull Text
Health and Medicine - Clinical Endocrinology and Diabetes; New Findings from Johannes Gutenberg-University in Clinical Endocrinology and Diabetes Provides New Insights (Novel Mutations in the NKX2.1 g...
Publisher:Atlanta: NewsRx
Journal title:Obesity, Fitness & Wellness Week, 2018, p.4308
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Newsletter articlesFull Text
Diabetes - Endocrinology and Diabetes; New Data from Johannes Gutenberg-University School of Medicine Illuminate Findings in Endocrinology and Diabetes (Novel Mutations in the NKX2.1 gene and the PAX8...
Publisher:Atlanta: NewsRx
Journal title:Diabetes Week, 2017, p.176
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Newsletter articlesFull Text
Congenital Diseases and Conditions - Congenital Hypothyroidism; Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation (S54C) of the PAX8 Gene in a Family...
Publisher:Atlanta: NewsRx
Journal title:Pediatrics Week, 2016, p.325
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ReportsFull Text
Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Indiv...
Publisher:NewsRX LLC
Journal title:Pediatrics Week, 2016, p.325
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Newsletter articlesFull Text
New Data from Johannes Gutenberg-University School of Medicine Illuminate Findings in Endocrinology and Diabetes (Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid...
Publisher:NewsRX LLC
Journal title:Diabetes Week, 2017, p.176
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Initial screening of the rs104893657 variant of the PAX8 gene in women with hypothyroidism from Northeastern Slovakia

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Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant

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Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands

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Comparative genomics reveals a functional thyroid-specific element in the far upstream region of the PAX8 gene

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Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism

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Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect

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Recovery of NIS expression in thyroid cancer cells by overexpression of Pax8 gene

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Thyroid hormone receptor α1: a novel regulator of thyroid cancer cell differentiation

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Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank

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PAX8 regulon in human ovarian cancer links lineage dependency with epigenetic vulnerability to HDAC inhibitors

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PAX8 expression in high-grade serous ovarian cancer positively regulates attachment to ECM via Integrin β3

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Genetic variant in CACNA1C is associated with PTSD in traumatized police officers

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New Findings from Johannes Gutenberg-University in Clinical Endocrinology and Diabetes Provides New Insights (Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid Synd...

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Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affecte...

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Screening for Pax8 Mutations in Patients with Congenital Hypothyroidism in South-West Germany

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Health and Medicine - Clinical Endocrinology and Diabetes; New Findings from Johannes Gutenberg-University in Clinical Endocrinology and Diabetes Provides New Insights (Novel Mutations in the NKX2.1 g...

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Diabetes - Endocrinology and Diabetes; New Data from Johannes Gutenberg-University School of Medicine Illuminate Findings in Endocrinology and Diabetes (Novel Mutations in the NKX2.1 gene and the PAX8...

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Congenital Diseases and Conditions - Congenital Hypothyroidism; Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation (S54C) of the PAX8 Gene in a Family...

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Studies in the Area of Congenital Hypothyroidism Reported from Tel Aviv University [A Novel Mutation of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Indiv...

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New Data from Johannes Gutenberg-University School of Medicine Illuminate Findings in Endocrinology and Diabetes (Novel Mutations in the NKX2.1 gene and the PAX8 gene in a Boy with Brain-Lung-Thyroid...

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