| scholarly article | Q13442814 |
| P50 | author | Ana Claudia Latronico Xavier | Q42715065 |
| Berenice Bilharinho Mendonca | Q42957618 | ||
| P2093 | author name string | Andrew Dauber | |
| Joel N Hirschhorn | |||
| Ursula B Kaiser | |||
| Rona S Carroll | |||
| Sekoni D Noel | |||
| Francis de Zegher | |||
| Carlos Alberto Longui | |||
| Cristiane Kochi | |||
| Victor M Navarro | |||
| Vinicius N Brito | |||
| Priscilla Cukier | |||
| Ana Paula Abreu | |||
| Delanie B Macedo | |||
| Luciana R Montenegro | |||
| Dominique Beckers | |||
| Tânia Rodrigues | |||
| Iain R Thompson | |||
| John C Gill | |||
| Priscila C Gagliardi | |||
| P2860 | cites work | Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus | Q46134005 |
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| Prader-Willi syndrome. | Q51826464 | ||
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| Normal ranges for immunochemiluminometric gonadotropin assays | Q61647839 | ||
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| Mutations of the KISS1 gene in disorders of puberty | Q24618754 | ||
| Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies | Q24628801 | ||
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| Reproductive Hormone-Dependent and -Independent Contributions to Developmental Changes in Kisspeptin in GnRH-Deficient Hypogonadal Mice | Q33651181 | ||
| The vertebrate makorin ubiquitin ligase gene family has been shaped by large-scale duplication and retroposition from an ancestral gonad-specific, maternal-effect gene | Q33776161 | ||
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| Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools | Q35708502 | ||
| Increased neurokinin B (Tac2) expression in the mouse arcuate nucleus is an early marker of pubertal onset with differential sensitivity to sex steroid-negative feedback than Kiss1. | Q36439417 | ||
| Whole exome sequencing reveals a novel mutation in CUL7 in a patient with an undiagnosed growth disorder | Q36472836 | ||
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| What controls the timing of puberty? An update on progress from genetic investigation | Q37356901 | ||
| Regulation of gonadotropin-releasing hormone secretion by kisspeptin/dynorphin/neurokinin B neurons in the arcuate nucleus of the mouse | Q37475488 | ||
| The recent genetics of hypogonadotrophic hypogonadism - novel insights and new questions | Q37589689 | ||
| Gene expression profiling of hypothalamic hamartomas: a search for genes associated with central precocious puberty | Q38295674 | ||
| Analysis of gonadotropin-releasing hormone gene structure in families with familial central precocious puberty and idiopathic hypogonadotropic hypogonadism | Q45682677 | ||
| P433 | issue | 26 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | precocious puberty | Q224513 |
| P304 | page(s) | 2467-2475 | |
| P577 | publication date | 2013-06-05 | |
| P1433 | published in | The New England Journal of Medicine | Q582728 |
| P1476 | title | Central precocious puberty caused by mutations in the imprinted gene MKRN3 | |
| P478 | volume | 368 |
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| Q34443581 | A novel MKRN3 missense mutation causing familial precocious puberty |
| Q89938726 | A novel MKRN3 nonsense mutation causing familial central precocious puberty |
| Q99590827 | A novel heterozygous MKRN3 nonsense mutation in a Chinese girl with idiopathic central precocious puberty: A case report |
| Q51812952 | Age at menarche: 50-year socioeconomic trends among US-born black and white women. |
| Q89818752 | Age of puberty and Sleep duration: Observational and Mendelian randomization study |
| Q26741326 | An update on the genetic causes of central precocious puberty |
| Q55015001 | Application of droplet digital PCR in the analysis of genome integration and organization of the transgene in BAC transgenic mice. |
| Q64967731 | Association between MKRN3 and LIN28B polymorphisms and precocious puberty. |
| Q90735347 | Association of blood leukocyte DNA methylation at LINE-1 and growth-related candidate genes with pubertal onset and progression |
| Q58718047 | Associations among IGF-1, IGF2, IGF-1R, IGF-2R, IGFBP-3, insulin genetic polymorphisms and central precocious puberty in girls |
| Q57632339 | Avanços na etiologia, no diagnóstico e no tratamento da puberdade precoce central |
| Q38725191 | Causes, diagnosis, and treatment of central precocious puberty |
| Q88312340 | Central Precocious Puberty - Management and Long-term Outcomes |
| Q64929890 | Central Precocious Puberty Caused by a Heterozygous Deletion in the MKRN3 Promoter Region. |
| Q54943308 | Central Precocious Puberty: Update on Diagnosis and Treatment. |
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| Q38837184 | Central precocious puberty: revisiting the diagnosis and therapeutic management. |
| Q89072505 | Characterization of the dynamic change of microRNA expression in mice hypothalamus during the time of female puberty |
| Q51279052 | Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty. |
| Q42351562 | Clinical phenotypes of MAGEL2 mutations and deletions |
| Q35100466 | Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. |
| Q46561759 | Conservation of imprinting of MKRN3 and NAP1L5 in rabbits |
| Q36733625 | Continuation of gradual weight gain necessary for the onset of puberty may be responsible for obesity later in life |
| Q38839109 | Control of puberty onset and fertility by gonadotropin-releasing hormone neurons |
| Q89341662 | Contrôle de l’axe gonadotrope : nouveaux aspects physiologiques et thérapeutiques: Control of the gonadotrope axis: new physiologic and therapeutic aspects |
| Q36176419 | DNA Methylation Patterns in the Hypothalamus of Female Pubertal Goats |
| Q38582557 | Decade in review-paediatric endocrinology: New genes, new therapies |
| Q36404781 | Decade in review-reproductive endocrinology: Understanding reproductive endocrine disorders |
| Q92904097 | Delayed Puberty-Phenotypic Diversity, Molecular Genetic Mechanisms, and Recent Discoveries |
| Q38319957 | Developmental variations in environmental influences including endocrine disruptors on pubertal timing and neuroendocrine control: Revision of human observations and mechanistic insight from rodents |
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| Q37482383 | Genetic Variations of the KISS1R Gene in Korean Girls with Central Precocious Puberty. |
| Q39976795 | Genetic variations altering FSH action affect circulating hormone levels as well as follicle growth in healthy peripubertal girls |
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| Q90633174 | Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan |
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| Q30277350 | Increases in Sex Hormones during Anti-Tumor Necrosis Factor α Therapy in Adolescents with Crohn's Disease |
| Q28088772 | Insights from exome sequencing for endocrine disorders |
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| Q47620141 | Kisspeptin and Neurokinin B Signaling Network Underlies the Pubertal Increase in GnRH Release in Female Rhesus Monkeys |
| Q34468572 | Large-scale whole-genome sequencing of the Icelandic population |
| Q64244074 | MKRN3 Interacts With Several Proteins Implicated in Puberty Timing but Does Not Influence Expression |
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| Q58608069 | Makorin 1 Regulates Developmental Timing in Drosophila |
| Q36744063 | Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans |
| Q95301860 | Metabolic regulation of kisspeptin - the link between energy balance and reproduction |
| Q59327034 | Methylome profiling of healthy and central precocious puberty girls |
| Q47110759 | Mkrn3 functions as a novel ubiquitin E3 ligase to inhibit Nptx1 during puberty initiation |
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| Q51629774 | Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes. |
| Q40754250 | Mutation of kisspeptin 1 gene in children with precocious puberty in isfahan city. |
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| Q64055545 | Mutations in Central Precocious Puberty: A Systematic Review and Meta-Analysis |
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| Q36431823 | Neuroestradiol in the Stalk Median Eminence of Female Rhesus Macaques Decreases in Association With Puberty Onset |
| Q37445958 | New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain |
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| Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
| Q47821601 | Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty. |
| Q38238174 | Perspectives in Pediatric Pathology, Chapter 15. Macrorchidism as the Expression of Several Congenital and Acquired Pathologies |
| Q64094464 | Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis |
| Q41526111 | Precocious Puberty or Premature Thelarche: Analysis of a Large Patient Series in a Single Tertiary Center with Special Emphasis on 6- to 8-Year-Old Girls |
| Q64264929 | Precocious and Early Central Puberty in Children With Pre-existing Medical Conditions: A Single Center Study |
| Q38202811 | Pros and cons of GnRHa treatment for early puberty in girls |
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| Q28116130 | Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations |
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| Q44549112 | Reproductive endocrinology: novel mutations linked to central precocious puberty |
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| Q52608499 | STAT6, PBX2, and PBRM1 Emerge as Predicted Regulators of 452 Differentially Expressed Genes Associated With Puberty in Brahman Heifers. |
| Q53359509 | Sexual dichotomy of gonadal function in Prader-Willi syndrome from early infancy through the fourth decade. |
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| Q35850430 | Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B) |
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| Q36068731 | Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23 |
| Q92993693 | Syndromic Disorders Caused by Disturbed Human Imprinting |
| Q91782182 | The Genetic Basis of Delayed Puberty |
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| Q33701516 | The first Japanese case of central precocious puberty with a novel MKRN3 mutation |
| Q36525006 | The genetics of pubertal timing in the general population: recent advances and evidence for sex-specificity |
| Q39157599 | The mystery of puberty initiation: genetics and epigenetics of idiopathic central precocious puberty (ICPP). |
| Q54941492 | The tempo of human childhood: a maternal foot on the accelerator, a paternal foot on the brake. |
| Q37334672 | Time Course of Central Precocious Puberty Development Caused by an MKRN3 Gene Mutation: A Prismatic Case. |
| Q60922548 | Timing mechanism of sexually dimorphic nervous system differentiation |
| Q51352634 | Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious Puberty. |
| Q97070248 | Unravelling the role of epigenetics in reproductive adaptations to early-life environment |
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