229 related articles for article (PubMed ID: 36729644)
1. Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadism.
Cotellessa L; Marelli F; Duminuco P; Adamo M; Papadakis GE; Bartoloni L; Sato N; Lang-Muritano M; Troendle A; Dhillo WS; Morelli A; Guarnieri G; Pitteloud N; Persani L; Bonomi M; Giacobini P; Vezzoli V
JCI Insight; 2023 Mar; 8(5):. PubMed ID: 36729644
[TBL] [Abstract][Full Text] [Related]
2. Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism.
Messina A; Pulli K; Santini S; Acierno J; Känsäkoski J; Cassatella D; Xu C; Casoni F; Malone SA; Ternier G; Conte D; Sidis Y; Tommiska J; Vaaralahti K; Dwyer A; Gothilf Y; Merlo GR; Santoni F; Niederländer NJ; Giacobini P; Raivio T; Pitteloud N
Am J Hum Genet; 2020 Jan; 106(1):58-70. PubMed ID: 31883645
[TBL] [Abstract][Full Text] [Related]
3. Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism.
Malone SA; Papadakis GE; Messina A; Mimouni NEH; Trova S; Imbernon M; Allet C; Cimino I; Acierno J; Cassatella D; Xu C; Quinton R; Szinnai G; Pigny P; Alonso-Cotchico L; Masgrau L; Maréchal JD; Prevot V; Pitteloud N; Giacobini P
Elife; 2019 Jul; 8():. PubMed ID: 31291191
[TBL] [Abstract][Full Text] [Related]
4. The terminal nerve plays a prominent role in GnRH-1 neuronal migration independent from proper olfactory and vomeronasal connections to the olfactory bulbs.
Taroc EZM; Prasad A; Lin JM; Forni PE
Biol Open; 2017 Oct; 6(10):1552-1568. PubMed ID: 28970231
[TBL] [Abstract][Full Text] [Related]
5. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Barraud S; Delemer B; Poirsier-Violle C; Bouligand J; Mérol JC; Grange F; Higel-Chaufour B; Decoudier B; Zalzali M; Dwyer AA; Acierno JS; Pitteloud N; Millar RP; Young J
Neuroendocrinology; 2021; 111(1-2):99-114. PubMed ID: 32074614
[TBL] [Abstract][Full Text] [Related]
6. Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
Sugisawa C; Taniyama M; Sato T; Takahashi Y; Hasegawa T; Narumi S
Endocr J; 2022 Jul; 69(7):831-838. PubMed ID: 35236788
[TBL] [Abstract][Full Text] [Related]
7. The role of semaphorin signaling in the etiology of hypogonadotropic hypogonadism.
Lettieri A; Oleari R; Gimmelli J; ANDRé V; Cariboni A
Minerva Endocrinol; 2016 Jun; 41(2):266-78. PubMed ID: 26940457
[TBL] [Abstract][Full Text] [Related]
8. The Differential Roles for Neurodevelopmental and Neuroendocrine Genes in Shaping GnRH Neuron Physiology and Deficiency.
Oleari R; Massa V; Cariboni A; Lettieri A
Int J Mol Sci; 2021 Aug; 22(17):. PubMed ID: 34502334
[TBL] [Abstract][Full Text] [Related]
9. Kallmann syndrome and idiopathic hypogonadotropic hypogonadism: The role of semaphorin signaling on GnRH neurons.
Cariboni A; Balasubramanian R
Handb Clin Neurol; 2021; 182():307-315. PubMed ID: 34266601
[TBL] [Abstract][Full Text] [Related]
10. Dysregulation of Semaphorin7A/β1-integrin signaling leads to defective GnRH-1 cell migration, abnormal gonadal development and altered fertility.
Messina A; Ferraris N; Wray S; Cagnoni G; Donohue DE; Casoni F; Kramer PR; Derijck AA; Adolfs Y; Fasolo A; Pasterkamp RJ; Giacobini P
Hum Mol Genet; 2011 Dec; 20(24):4759-74. PubMed ID: 21903667
[TBL] [Abstract][Full Text] [Related]
11. DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Bouilly J; Messina A; Papadakis G; Cassatella D; Xu C; Acierno JS; Tata B; Sykiotis G; Santini S; Sidis Y; Elowe-Gruau E; Phan-Hug F; Hauschild M; Bouloux PM; Quinton R; Lang-Muritano M; Favre L; Marino L; Giacobini P; Dwyer AA; Niederländer NJ; Pitteloud N
Hum Mol Genet; 2018 Jan; 27(2):359-372. PubMed ID: 29202173
[TBL] [Abstract][Full Text] [Related]
12. Gonadotropin-releasing hormone immunoreactivity in the nasal epithelia of adults with Kallmann's syndrome and isolated hypogonadotropic hypogonadism and in the early midtrimester human fetus.
Quinton R; Hasan W; Grant W; Thrasivoulou C; Quiney RE; Besser GM; Bouloux PM
J Clin Endocrinol Metab; 1997 Jan; 82(1):309-14. PubMed ID: 8989279
[TBL] [Abstract][Full Text] [Related]
13. The complex genetic basis of congenital hypogonadotropic hypogonadism.
Vezzoli V; Duminuco P; Bassi I; Guizzardi F; Persani L; Bonomi M
Minerva Endocrinol; 2016 Jun; 41(2):223-39. PubMed ID: 26934720
[TBL] [Abstract][Full Text] [Related]
14. Defective gonadotropin-releasing hormone neuron migration in mice lacking SEMA3A signalling through NRP1 and NRP2: implications for the aetiology of hypogonadotropic hypogonadism.
Cariboni A; Davidson K; Rakic S; Maggi R; Parnavelas JG; Ruhrberg C
Hum Mol Genet; 2011 Jan; 20(2):336-44. PubMed ID: 21059704
[TBL] [Abstract][Full Text] [Related]
15. The initiation and maintenance of gonadotropin-releasing hormone neuron identity in congenital hypogonadotropic hypogonadism.
Chung WC; Tsai PS
Front Endocrinol (Lausanne); 2023; 14():1166132. PubMed ID: 37181038
[TBL] [Abstract][Full Text] [Related]
16. Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.
Brioude F; Bouligand J; Trabado S; Francou B; Salenave S; Kamenicky P; Brailly-Tabard S; Chanson P; Guiochon-Mantel A; Young J
Eur J Endocrinol; 2010 May; 162(5):835-51. PubMed ID: 20207726
[TBL] [Abstract][Full Text] [Related]
17. Genetics defects in GNRH1: a paradigm of hypothalamic congenital gonadotropin deficiency.
Bouligand J; Ghervan C; Trabado S; Brailly-Tabard S; Guiochon-Mantel A; Young J
Brain Res; 2010 Dec; 1364():3-9. PubMed ID: 20887715
[TBL] [Abstract][Full Text] [Related]
18. Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease.
Cangiano B; Swee DS; Quinton R; Bonomi M
Hum Genet; 2021 Jan; 140(1):77-111. PubMed ID: 32200437
[TBL] [Abstract][Full Text] [Related]
19. Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Boehm U; Bouloux PM; Dattani MT; de Roux N; Dodé C; Dunkel L; Dwyer AA; Giacobini P; Hardelin JP; Juul A; Maghnie M; Pitteloud N; Prevot V; Raivio T; Tena-Sempere M; Quinton R; Young J
Nat Rev Endocrinol; 2015 Sep; 11(9):547-64. PubMed ID: 26194704
[TBL] [Abstract][Full Text] [Related]
20. GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in
Neocleous V; Fanis P; Toumba M; Tanteles GA; Schiza M; Cinarli F; Nicolaides NC; Oulas A; Spyrou GM; Mantzoros CS; Vlachakis D; Skordis N; Phylactou LA
Front Endocrinol (Lausanne); 2020; 11():626. PubMed ID: 32982993
[No Abstract] [Full Text] [Related]
[Next] [New Search]
