Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD)

Michela Godi; Simona Mellone; Luigi Tiradani; Rita Marabese; Claudio Bardelli; Mariacarolina Salerno; Flavia Prodam; Simonetta Bellone; Antonella Petri; Patricia Momigliano-Richiardi; Gianni Bona; Mara Giordano

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Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD)

机译：PROP1基因的内含子1内的功能性SNP有助于联合生长激素缺乏症（CPHD）

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Context:Mutations within the PROP1 gene represent one of the main causes of familial combined pituitary hormone deficiency (CPHD). However, most of the cases are sporadic with an unknown genetic cause.

机译：背景：PROP1基因内的突变是家族性垂体激素缺乏症（CPHD）的主要原因之一。但是，大多数情况是零星的，遗传原因未知。

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《The journal of clinical endocrinology and metabolism》 |2012年第9期|共7页
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Michela Godi; Simona Mellone; Luigi Tiradani; Rita Marabese; Claudio Bardelli; Mariacarolina Salerno; Flavia Prodam; Simonetta Bellone; Antonella Petri; Patricia Momigliano-Richiardi; Gianni Bona; Mara Giordano;
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1. Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD) [J] . Michela Godi, Simona Mellone, Luigi Tiradani, The journal of clinical endocrinology and metabolism . 2012,第9期

机译：PROP1基因的内含子1内的功能性SNP有助于联合生长激素缺乏症（CPHD）
2. Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD). [J] . Kelberman D, Turton JP, Woods KS, Clinical Endocrinology . 2009,第1期

机译：与垂体激素联合缺乏症（CPHD）相关的新型PROP1突变的分子分析。
3. Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency [J] . Fatma Derya Bulut, Semine ?zdemir Dilek, Damla Kotan, Journal of Clinical Research in Pediatric Endocrinology . 2020,第3期

机译：转录因子中的突变在土耳其患者组合垂体激素缺乏的土耳其患者队列中的突变 /斜体>
4. The effect of SNP polymorphisms in growth hormone gene on weight and linear growth in crossbred Red Angus × Kalmyk heifers [C] . Foat Kayumov, Vladimir Kosilov, Nikolay Gerasimov, International Scientific and Practical Conference on Digitization of Agriculture - Development Strategy . 2019

机译：SNP多态性在生长激素基因对杂交红松×Kalmyk小母牛重量和线性生长的影响
5. Plasticity of pituitary hormone secretion, expression and cell numbers within the anterior pituitary glands of human growth hormone-releasing hormone transgenic mice: Focus on galanin, growth hormone, and prolactin. [D] . Moore, Joseph Patrick, Jr. 1997

机译：人类生长激素释放激素转基因小鼠的垂体前叶垂体激素分泌，表达和细胞数量的可塑性：专注于甘丙肽，生长激素和催乳激素。
6. Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations [O] . Petra Dusatkova, Roland Pfäffle, Milton R Brown, 2016

机译：两个最普遍的PROP1基因变异的发生导致21个人口的合并垂体激素缺乏
7. Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD). [O] . Godi M, Mellone S, Tiradani L, 2012

机译：pROp1基因的内含子1内的功能性sNp有助于组合生长激素缺乏症（CpHD）。

Functional SNPs within the Intron 1 of the PROP1 Gene Contribute to Combined Growth Hormone Deficiency (CPHD)

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