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1999 1
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117 results

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Page 1
TBX19 is overexpressed in colorectal cancer and associated with lymph node metastasis.
Ando J, Saito M, Imai JI, Ito E, Yanagisawa Y, Honma R, Saito K, Tachibana K, Momma T, Ohki S, Ohtake T, Watanabe S, Waguri S, Kono K, Takenoshita S. Ando J, et al. Fukushima J Med Sci. 2017 Dec 19;63(3):141-151. doi: 10.5387/fms.2017-08. Epub 2017 Dec 1. Fukushima J Med Sci. 2017. PMID: 29199261 Free PMC article.
The expression of TBX19 mRNA was not correlated with that of TBX19 protein in tissue sample taken from the CRC patients. ...These results suggest that the expression of TBX19 protein is not correlated with the expression of TBX19 mRNA. ...
The expression of TBX19 mRNA was not correlated with that of TBX19 protein in tissue sample taken from the CRC patients. ...Th …
Pangenomic Classification of Pituitary Neuroendocrine Tumors.
Neou M, Villa C, Armignacco R, Jouinot A, Raffin-Sanson ML, Septier A, Letourneur F, Diry S, Diedisheim M, Izac B, Gaspar C, Perlemoine K, Verjus V, Bernier M, Boulin A, Emile JF, Bertagna X, Jaffrezic F, Laloe D, Baussart B, Bertherat J, Gaillard S, Assié G. Neou M, et al. Cancer Cell. 2020 Jan 13;37(1):123-134.e5. doi: 10.1016/j.ccell.2019.11.002. Epub 2019 Dec 26. Cancer Cell. 2020. PMID: 31883967 Free article.
Pituitary neuroendocrine tumors (PitNETs) are common, with five main histological subtypes: lactotroph, somatotroph, and thyrotroph (POU1F1/PIT1 lineage); corticotroph (TBX19/TPIT lineage); and gonadotroph (NR5A1/SF1 lineage). We report a comprehensive pangenomic classific …
Pituitary neuroendocrine tumors (PitNETs) are common, with five main histological subtypes: lactotroph, somatotroph, and thyrotroph (POU1F1/ …
A novel TBX19 gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin.
Charnay T, Mougel G, Amouroux C, Gueorguieva I, Joubert F, Pertuit M, Reynaud R, Barlier A, Brue T, Saveanu A. Charnay T, et al. Front Endocrinol (Lausanne). 2023 Feb 15;13:1080649. doi: 10.3389/fendo.2022.1080649. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36890856 Free PMC article.
We describe a new variant of the main TBX19 transcript (NM 005149.3, c.840del (p.(Glu280Asp fs*27)), classified as pathogenic, whose pathogenicity is assumed to be due to nonsense mediated decay leading to non-expression of T-box transcription factor TBX19. Moreover …
We describe a new variant of the main TBX19 transcript (NM 005149.3, c.840del (p.(Glu280Asp fs*27)), classified as pathogenic, whose …
Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature.
Abali ZY, Yesil G, Kirkgoz T, Kaygusuz SB, Eltan M, Turan S, Bereket A, Guran T. Abali ZY, et al. Hormones (Athens). 2019 Jun;18(2):229-236. doi: 10.1007/s42000-019-00096-7. Epub 2019 Feb 12. Hormones (Athens). 2019. PMID: 30747411 Review.
BACKGROUND: Biallelic mutations in the TBX19 gene cause severe early-onset adrenal failure due to isolated ACTH deficiency (IAD). ...Whole exome sequencing revealed a novel homozygous c.302G > A (W101*) mutation in the TBX19 gene. CONCLUSION: We report a new muta …
BACKGROUND: Biallelic mutations in the TBX19 gene cause severe early-onset adrenal failure due to isolated ACTH deficiency (IAD). ... …
A Rare Cause of Adrenal Insufficiency - Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature.
Kardelen Al AD, Poyrazoğlu Ş, Aslanger A, Yeşil G, Ceylaner S, Baş F, Darendeliler F. Kardelen Al AD, et al. Horm Res Paediatr. 2019;92(6):395-403. doi: 10.1159/000506740. Epub 2020 Apr 28. Horm Res Paediatr. 2019. PMID: 32344415 Free article. Review.
We describe 2 patients, 1 with a reported and 1 with a novel TBX19 mutation, and present information about the long-term follow-up of these patients. ...CONCLUSION: Congenital IAD can be life-threatening if it is not recognized and treated early. TBX19 mutations sho …
We describe 2 patients, 1 with a reported and 1 with a novel TBX19 mutation, and present information about the long-term follow-up of …
Tbx19, a tissue-selective regulator of POMC gene expression.
Liu J, Lin C, Gleiberman A, Ohgi KA, Herman T, Huang HP, Tsai MJ, Rosenfeld MG. Liu J, et al. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8674-9. doi: 10.1073/pnas.141234898. Epub 2001 Jul 10. Proc Natl Acad Sci U S A. 2001. PMID: 11447259 Free PMC article.
The critical transcriptional determinants of the two pituitary cell types that express the pro-opiomelanocortin (POMC) gene, the anterior lobe corticotropes, producing adrenocorticotropin, and the intermediate lobe melanotropes, producing melanocyte-stimulating hormone (MSH alpha …
The critical transcriptional determinants of the two pituitary cell types that express the pro-opiomelanocortin (POMC) gene, the anterior lo …
[Analysis of TBX19 gene variant in a child with congenital isolated adrenocorticotropic hormone deficiency].
Wu S, Chen Q, Shen L, Wei H, Chen Y. Wu S, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jan 10;38(1):59-62. doi: 10.3760/cma.j.cn511374-20191107-00563. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33423260 Chinese.
CONCLUSION: Congenital IAD due to variants of the TBX19 gene is a rare autosomal recessive disease. It is characterized by low plasma adrenocorticotropic hormone and cortisol levels but normal levels of other pituitary hormones. ...Hydrocortisone replacement is effective. …
CONCLUSION: Congenital IAD due to variants of the TBX19 gene is a rare autosomal recessive disease. It is characterized by low plasma …
T-box transcription factor 19 promotes hepatocellular carcinoma metastasis through upregulating EGFR and RAC1.
Ji X, Chen X, Zhang B, Xie M, Zhang T, Luo X, Liu D, Feng Y, Wang Y, Sun M, Li C, Huang W, Xia L. Ji X, et al. Oncogene. 2022 Apr;41(15):2225-2238. doi: 10.1038/s41388-022-02249-2. Epub 2022 Feb 26. Oncogene. 2022. PMID: 35217793
TBX19 expression was markedly upregulated in HCC tissues and elevated TBX19 expression predicted poor prognosis. ...Patients with positive coexpression of TBX19/EGFR or TBX19/RAC1 displayed the poorest prognosis. In conclusion, EGF/EGFR signaling upreg …
TBX19 expression was markedly upregulated in HCC tissues and elevated TBX19 expression predicted poor prognosis. ...Patients w …
A serious and unusual presentation of congenital isolated ACTH deficiency due to TBX19 mutation, beyond the neonatal period.
Vieira IH, Mourinho Bala N, Ramos F, Dinis I, Cardoso R, Caetano JS, Rodrigues D, Paiva I, Mirante A. Vieira IH, et al. Endocrinol Diabetes Metab Case Rep. 2022 Sep 1;2022:22-0277. doi: 10.1530/EDM-22-0277. Online ahead of print. Endocrinol Diabetes Metab Case Rep. 2022. PMID: 36070412 Free PMC article.
The genetic investigation was requested and compound heterozygous mutations in TBX19 were detected. This is a rare case of presentation of TBX19 mutation outside the neonatal period and in the setting of acute disease, which presented a diagnostic challenge. LEARNIN …
The genetic investigation was requested and compound heterozygous mutations in TBX19 were detected. This is a rare case of presentati …
Congenital Isolated ACTH Deficiency Caused by TBX19 Gene Mutation: A Family Report.
Peng C, Sun G, Tang Z, Hou X. Peng C, et al. Front Pediatr. 2020 Jan 10;7:546. doi: 10.3389/fped.2019.00546. eCollection 2019. Front Pediatr. 2020. PMID: 31998673 Free PMC article.
We reported on two siblings with a homozygous mutation of the TBX19 gene, C.377 (exon2) C>T, p. P126L. Their parents had heterozygous mutations on the same locus. ...
We reported on two siblings with a homozygous mutation of the TBX19 gene, C.377 (exon2) C>T, p. P126L. Their parents had heterozyg …
117 results