These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 26186301)

  • 1. Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene.
    Wabitsch M; Funcke JB; von Schnurbein J; Denzer F; Lahr G; Mazen I; El-Gammal M; Denzer C; Moss A; Debatin KM; Gierschik P; Mistry V; Keogh JM; Farooqi IS; Moepps B; Fischer-Posovszky P
    J Clin Endocrinol Metab; 2015 Sep; 100(9):3227-30. PubMed ID: 26186301
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient.
    Mazen I; El-Gammal M; Abdel-Hamid M; Amr K
    Mol Genet Metab; 2009 Aug; 97(4):305-8. PubMed ID: 19427251
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biologically inactive leptin and early-onset extreme obesity.
    Wabitsch M; Funcke JB; Lennerz B; Kuhnle-Krahl U; Lahr G; Debatin KM; Vatter P; Gierschik P; Moepps B; Fischer-Posovszky P
    N Engl J Med; 2015 Jan; 372(1):48-54. PubMed ID: 25551525
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The p. N103K mutation of leptin (LEP) gene and severe early onset obesity in Pakistan.
    Shabana ; Hasnain S
    Biol Res; 2016 Apr; 49():23. PubMed ID: 27075752
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital Leptin Deficiency and Leptin Gene Missense Mutation Found in Two Colombian Sisters with Severe Obesity.
    Yupanqui-Lozno H; Bastarrachea RA; Yupanqui-Velazco ME; Alvarez-Jaramillo M; Medina-Méndez E; Giraldo-Peña AP; Arias-Serrano A; Torres-Forero C; Garcia-Ordoñez AM; Mastronardi CA; Restrepo CM; Rodriguez-Ayala E; Nava-Gonzalez EJ; Arcos-Burgos M; Kent JW; Cole SA; Licinio J; Celis-Regalado LG
    Genes (Basel); 2019 May; 10(5):. PubMed ID: 31067764
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity.
    Mazen I; El-Gammal M; Abdel-Hamid M; Farooqi IS; Amr K
    Mol Genet Metab; 2011 Apr; 102(4):461-4. PubMed ID: 21306929
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
    Farooqi IS; Wangensteen T; Collins S; Kimber W; Matarese G; Keogh JM; Lank E; Bottomley B; Lopez-Fernandez J; Ferraz-Amaro I; Dattani MT; Ercan O; Myhre AG; Retterstol L; Stanhope R; Edge JA; McKenzie S; Lessan N; Ghodsi M; De Rosa V; Perna F; Fontana S; Barroso I; Undlien DE; O'Rahilly S
    N Engl J Med; 2007 Jan; 356(3):237-47. PubMed ID: 17229951
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy.
    Gibson WT; Farooqi IS; Moreau M; DePaoli AM; Lawrence E; O'Rahilly S; Trussell RA
    J Clin Endocrinol Metab; 2004 Oct; 89(10):4821-6. PubMed ID: 15472169
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leptin deficiency and leptin gene mutations in obese children from Pakistan.
    Fatima W; Shahid A; Imran M; Manzoor J; Hasnain S; Rana S; Mahmood S
    Int J Pediatr Obes; 2011 Oct; 6(5-6):419-27. PubMed ID: 21854111
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Early-onset severe obesity due to homozygous p.R105W (c313C> T) mutation in leptin gene in Turkish siblings: Two cases reports.
    Fırat SN; Onay H
    Obes Res Clin Pract; 2021; 15(6):600-603. PubMed ID: 34802983
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Concordance of bioactive vs. total immunoreactive serum leptin levels in children with severe early onset obesity.
    Stanik J; Kratzsch J; Landgraf K; Scheuermann K; Spielau U; Gausche R; Gasperikova D; Kiess W; Körner A
    PLoS One; 2017; 12(5):e0178107. PubMed ID: 28542631
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe Early Onset Obesity due to a Novel Missense Mutation in Exon 3 of the Leptin Gene in an Infant from Northwest India.
    Dayal D; Seetharaman K; Panigrahi I; Muthuvel B; Agarwal A
    J Clin Res Pediatr Endocrinol; 2018 Jul; 10(3):274-278. PubMed ID: 29217499
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Changes in levels of peripheral hormones controlling appetite are inconsistent with hyperphagia in leptin-deficient subjects.
    Saeed S; Bech PR; Hafeez T; Alam R; Falchi M; Ghatei MA; Bloom SR; Arslan M; Froguel P
    Endocrine; 2014 Apr; 45(3):401-8. PubMed ID: 23824601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of novel LEPR mutations in Pakistani families with morbid childhood obesity.
    Niazi RK; Gjesing AP; Hollensted M; Have CT; Grarup N; Pedersen O; Ullah A; Shahid G; Ahmad W; Gul A; Hansen T
    BMC Med Genet; 2018 Nov; 19(1):199. PubMed ID: 30442103
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel homozygous leptin receptor mutation in an infant with monogenic obesity.
    Boro H; Bundela V; Mannar V; Nagendra L; Jain V; Jain B; Kumar S; Agstam S
    Pediatr Endocrinol Diabetes Metab; 2023; 29(2):118-123. PubMed ID: 37728464
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Potential role of gender specific effect of leptin receptor deficiency in an extended consanguineous family with severe early-onset obesity.
    Dehghani MR; Mehrjardi MYV; Dilaver N; Tajamolian M; Enayati S; Ebrahimi P; Amoli MM; Farooqi S; Maroofian R
    Eur J Med Genet; 2018 Aug; 61(8):465-467. PubMed ID: 29545012
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness.
    Fischer-Posovszky P; von Schnurbein J; Moepps B; Lahr G; Strauss G; Barth TF; Kassubek J; Mühleder H; Möller P; Debatin KM; Gierschik P; Wabitsch M
    J Clin Endocrinol Metab; 2010 Jun; 95(6):2836-40. PubMed ID: 20382689
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families.
    Saeed S; Butt TA; Anwer M; Arslan M; Froguel P
    Mol Genet Metab; 2012 May; 106(1):121-6. PubMed ID: 22463805
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of a novel genetically obese mouse model demonstrating early onset hyperphagia and hyperleptinemia.
    Nakahara K; Bannai M; Maruyama K; Suzuki Y; Okame R; Murakami N
    Am J Physiol Endocrinol Metab; 2013 Aug; 305(3):E451-63. PubMed ID: 23736543
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel mutation of the leptin gene in an Indian patient.
    Thakur S; Kumar A; Dubey S; Saxena R; Peters AN; Singhal A
    Clin Genet; 2014 Oct; 86(4):391-3. PubMed ID: 24304187
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.