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 *

142 related articles for article (PubMed ID: 35316681)

  • 1. The paradox of Prader-Willi syndrome revisited: Making sense of the phenotype.
    Holland A; Manning K; Whittington J
    EBioMedicine; 2022 Apr; 78():103952. PubMed ID: 35316681
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
    Brant JO; Riva A; Resnick JL; Yang TP
    Epigenetics; 2014 Nov; 9(11):1540-56. PubMed ID: 25482058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An unexpected function of the Prader-Willi syndrome imprinting center in maternal imprinting in mice.
    Wu MY; Jiang M; Zhai X; Beaudet AL; Wu RC
    PLoS One; 2012; 7(4):e34348. PubMed ID: 22496793
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The paradox of Prader-Willi syndrome: a genetic model of starvation.
    Holland A; Whittington J; Hinton E
    Lancet; 2003 Sep; 362(9388):989-91. PubMed ID: 14511934
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.
    Davies JR; Humby T; Dwyer DM; Garfield AS; Furby H; Wilkinson LS; Wells T; Isles AR
    Eur J Neurosci; 2015 Aug; 42(4):2105-13. PubMed ID: 26040449
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
    Duker AL; Ballif BC; Bawle EV; Person RE; Mahadevan S; Alliman S; Thompson R; Traylor R; Bejjani BA; Shaffer LG; Rosenfeld JA; Lamb AN; Sahoo T
    Eur J Hum Genet; 2010 Nov; 18(11):1196-201. PubMed ID: 20588305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
    Lee S; Wevrick R
    Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prader-Willi syndrome: reflections on seminal studies and future therapies.
    Chung MS; Langouët M; Chamberlain SJ; Carmichael GG
    Open Biol; 2020 Sep; 10(9):200195. PubMed ID: 32961075
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
    Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
    Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
    Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mechanistic insights into the genetics of affective psychosis from Prader-Willi syndrome.
    Aman LCS; Manning KE; Whittington JE; Holland AJ
    Lancet Psychiatry; 2018 Apr; 5(4):370-378. PubMed ID: 29352661
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.
    Muscogiuri G; Barrea L; Faggiano F; Maiorino MI; Parrillo M; Pugliese G; Ruggeri RM; Scarano E; Savastano S; Colao A;
    J Endocrinol Invest; 2021 Oct; 44(10):2057-2070. PubMed ID: 33891302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.
    Bittel DC; Kibiryeva N; McNulty SG; Driscoll DJ; Butler MG; White RA
    Am J Med Genet A; 2007 Mar; 143A(5):422-9. PubMed ID: 17036336
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
    Smith A
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.
    Brøndum-Nielsen K
    Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prader-Willi syndrome: advances in genetics, pathophysiology and treatment.
    Goldstone AP
    Trends Endocrinol Metab; 2004; 15(1):12-20. PubMed ID: 14693421
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
    Stefan M; Portis T; Longnecker R; Nicholls RD
    Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Development of the eating behaviour in Prader-Willi Syndrome: advances in our understanding.
    McAllister CJ; Whittington JE; Holland AJ
    Int J Obes (Lond); 2011 Feb; 35(2):188-97. PubMed ID: 20680019
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
    Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
    Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evolution of genomic imprinting with biparental care: implications for Prader-Willi and Angelman syndromes.
    Ubeda F
    PLoS Biol; 2008 Aug; 6(8):e208. PubMed ID: 18752349
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.