Terms: = Bone cancer AND SMAD4, JIP, Q13485, 4089, ENSG00000141646, MADH4, DPC4 AND Diagnosis
18 results:
1. Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study.
Jelsig AM; van Overeem Hansen T; Gede LB; Qvist N; Christensen LL; Lautrup CK; Ljungmann K; Christensen LT; Rønlund K; Tørring PM; Bertelsen B; Sunde L; Karstensen JG
Fam Cancer; 2023 Oct; 22(4):429-436. PubMed ID: 37354305
[TBL] [Abstract] [Full Text] [Related]
2. Endoscopic Endonasal Approach to Intraconal Orbital Tumors: Outcomes and Lessons Learned.
Sindwani R; Sreenath SB; Recinos PF
Laryngoscope; 2024 Jan; 134(1):47-55. PubMed ID: 37249188
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3. Phenotypic Differences in Juvenile Polyposis Syndrome With or Without a Disease-causing
MacFarland SP; Ebrahimzadeh JE; Zelley K; Begum L; Bass LM; Brand RE; Dudley B; Fishman DS; Ganzak A; Karloski E; Latham A; Llor X; Plon S; Riordan MK; Scollon SR; Stadler ZK; Syngal S; Ukaegbu C; Weiss JM; Yurgelun MB; Brodeur GM; Mamula P; Katona BW
Cancer Prev Res (Phila); 2021 Feb; 14(2):215-222. PubMed ID: 33097490
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4. Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review.
Gao XH; Li J; Zhao ZY; Xu XD; Du YQ; Yan HL; Liu LJ; Bai CG; Zhang W
BMC Gastroenterol; 2020 Jun; 20(1):167. PubMed ID: 32487124
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5. Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis.
Lecoquierre F; Cassinari K; Chambon P; Nicolas G; Malsa S; Marlin R; Assouline Y; Fléjou JF; Frebourg T; Houdayer C; Bera O; Baert-Desurmont S
Eur J Med Genet; 2020 Apr; 63(4):103773. PubMed ID: 31561016
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6. cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal cancer Syndromes in Childhood.
Achatz MI; Porter CC; Brugières L; Druker H; Frebourg T; Foulkes WD; Kratz CP; Kuiper RP; Hansford JR; Hernandez HS; Nathanson KL; Kohlmann WK; Doros L; Onel K; Schneider KW; Scollon SR; Tabori U; Tomlinson GE; Evans DGR; Plon SE
Clin Cancer Res; 2017 Jul; 23(13):e107-e114. PubMed ID: 28674119
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7. Statin Use After diagnosis of Colon cancer and Patient Survival.
Voorneveld PW; Reimers MS; Bastiaannet E; Jacobs RJ; van Eijk R; Zanders MMJ; Herings RMC; van Herk-Sukel MPP; Kodach LL; van Wezel T; Kuppen PJK; Morreau H; van de Velde CJH; Hardwick JCH; Liefers GJ
Gastroenterology; 2017 Aug; 153(2):470-479.e4. PubMed ID: 28512021
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8. Abnormal Uterine Bleeding Is Associated With Increased BMP7 Expression in Human Endometrium.
Richards EG; El-Nashar SA; Schoolmeester JK; Keeney GL; Mariani A; Hopkins MR; Dowdy SC; Daftary GS; Famuyide AO
Reprod Sci; 2017 May; 24(5):671-681. PubMed ID: 28142396
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9. Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing.
Chubb D; Broderick P; Frampton M; Kinnersley B; Sherborne A; Penegar S; Lloyd A; Ma YP; Dobbins SE; Houlston RS
J Clin Oncol; 2015 Feb; 33(5):426-32. PubMed ID: 25559809
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10. Juvenile polyposis syndrome: a study of genotype, phenotype, and long-term outcome.
Latchford AR; Neale K; Phillips RK; Clark SK
Dis Colon Rectum; 2012 Oct; 55(10):1038-43. PubMed ID: 22965402
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11. Juvenile polyposis syndrome.
Brosens LA; Langeveld D; van Hattem WA; Giardiello FM; Offerhaus GJ
World J Gastroenterol; 2011 Nov; 17(44):4839-44. PubMed ID: 22171123
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12. Genetic variation in the transforming growth factor-β signaling pathway and survival after diagnosis with colon and rectal cancer.
Slattery ML; Lundgreen A; Herrick JS; Wolff RK; Caan BJ
Cancer; 2011 Sep; 117(18):4175-83. PubMed ID: 21365634
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13. Juvenile polyps: recurrence in patients with multiple and solitary polyps.
Fox VL; Perros S; Jiang H; Goldsmith JD
Clin Gastroenterol Hepatol; 2010 Sep; 8(9):795-9. PubMed ID: 20580940
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14. Large genomic deletions of smad4, BMPR1A and PTEN in juvenile polyposis.
van Hattem WA; Brosens LA; de Leng WW; Morsink FH; Lens S; Carvalho R; Giardiello FM; Offerhaus GJ
Gut; 2008 May; 57(5):623-7. PubMed ID: 18178612
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15. Mutation screening in juvenile polyposis syndrome.
Pyatt RE; Pilarski R; Prior TW
J Mol Diagn; 2006 Feb; 8(1):84-8. PubMed ID: 16436638
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16. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
Sweet K; Willis J; Zhou XP; Gallione C; Sawada T; Alhopuro P; Khoo SK; Patocs A; Martin C; Bridgeman S; Heinz J; Pilarski R; Lehtonen R; Prior TW; Frebourg T; Teh BT; Marchuk DA; Aaltonen LA; Eng C
JAMA; 2005 Nov; 294(19):2465-73. PubMed ID: 16287957
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17. Juvenile polyposis: massive gastric polyposis is more common in madh4 mutation carriers than in BMPR1A mutation carriers.
Friedl W; Uhlhaas S; Schulmann K; Stolte M; Loff S; Back W; Mangold E; Stern M; Knaebel HP; Sutter C; Weber RG; Pistorius S; Burger B; Propping P
Hum Genet; 2002 Jul; 111(1):108-11. PubMed ID: 12136244
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18. Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes.
Zhou XP; Woodford-Richens K; Lehtonen R; Kurose K; Aldred M; Hampel H; Launonen V; Virta S; Pilarski R; Salovaara R; Bodmer WF; Conrad BA; Dunlop M; Hodgson SV; Iwama T; Järvinen H; Kellokumpu I; Kim JC; Leggett B; Markie D; Mecklin JP; Neale K; Phillips R; Piris J; Rozen P; Houlston RS; Aaltonen LA; Tomlinson IP; Eng C
Am J Hum Genet; 2001 Oct; 69(4):704-11. PubMed ID: 11536076
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