scholarly article | Q13442814 |
P2093 | author name string | Huifang Liu | |
Fengling Chen | |||
Xiangxin Kong | |||
P2860 | cites work | The effect of leptin on luteinizing hormone release is exerted in the zona incerta and mediated by melanin-concentrating hormone | Q38306905 |
Causes, diagnosis, and treatment of central precocious puberty | Q38725191 | ||
In silico analysis of a novel MKRN3 missense mutation in familial central precocious puberty. | Q40738493 | ||
Effects of NELL2 on the regulation of GnRH expression and puberty in female rats | Q42194972 | ||
Selective expression of Narp, a secreted neuronal pentraxin, in orexin neurons | Q44158613 | ||
Molecular and gene network analysis of thyroid transcription factor 1 (TTF1) and enhanced at puberty (EAP1) genes in patients with GnRH-dependent pubertal disorders. | Q45382794 | ||
NPTX1 regulates neural lineage specification from human pluripotent stem cells | Q47916005 | ||
A missense mutation in MKRN3 in a Danish girl with central precocious puberty and her brother with early puberty | Q48139111 | ||
Imprinting of a RING zinc-finger encoding gene in the mouse chromosome region homologous to the Prader-Willi syndrome genetic region | Q48242077 | ||
Expression of EAP1 and CUX1 in the hypothalamus of female rats and relationship with KISS1 and GnRH. | Q48702391 | ||
Releasing the brake on puberty. | Q50935565 | ||
Circulating MKRN3 Levels Decline During Puberty in Healthy Boys. | Q52670306 | ||
Circulating makorin ring-finger protein-3 (MKRN3) levels in healthy men and in men with hypogonadotropic hypogonadism | Q58035102 | ||
Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty | Q86363486 | ||
A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region | Q22009166 | ||
Mouse and human neuronal pentraxin 1 (NPTX1): conservation, genomic structure, and chromosomal localization | Q24315655 | ||
A new pathway in the control of the initiation of puberty: the MKRN3 gene | Q26861068 | ||
Structure of pentameric human serum amyloid P component | Q27731194 | ||
RING domain E3 ubiquitin ligases | Q27860546 | ||
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Central precocious puberty caused by mutations in the imprinted gene MKRN3. | Q34348835 | ||
Central precocious puberty in a girl and early puberty in her brother caused by a novel mutation in the MKRN3 gene | Q34398621 | ||
Low Frequency of MKRN3 Mutations in Central Precocious Puberty Among Korean Girls | Q34474893 | ||
Developmental changes in embryonic hypothalamic neurons during prenatal fat exposure | Q37175024 | ||
Pubertal development and regulation | Q37538376 | ||
New causes of central precocious puberty: the role of genetic factors. | Q38239266 | ||
Gene expression profiling of hypothalamic hamartomas: a search for genes associated with central precocious puberty | Q38295674 | ||
P433 | issue | 49 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 85102-85109 | |
P577 | publication date | 2017-07-18 | |
P1433 | published in | Oncotarget | Q1573155 |
P1476 | title | Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation | |
P478 | volume | 8 |
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