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Results: 1 to 20 of 59

Select item 232430141.

BMP system expression in GCs from polycystic ovary syndrome women and the in vitro effects of BMP4, BMP6, and BMP7 on GC steroidogenesis.

Khalaf M, Morera J, Bourret A, Reznik Y, Denoual C, Herlicoviez M, Mittre H, Benhaim A.

Eur J Endocrinol. 2013 Feb 20;168(3):437-44. doi: 10.1530/EJE-12-0891. Print 2013 Mar.

PMID:: 23243014; [PubMed - indexed for MEDLINE]

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Select item 230444162.

Fibroblast growth factor 2 inhibits up-regulation of bone morphogenic proteins and their receptors during osteoblastic differentiation of human mesenchymal stem cells.

Biver E, Soubrier AS, Thouverey C, Cortet B, Broux O, Caverzasio J, Hardouin P.

Biochem Biophys Res Commun. 2012 Nov 2;427(4):737-42. doi: 10.1016/j.bbrc.2012.09.129. Epub 2012 Oct 5.

PMID:: 23044416; [PubMed - indexed for MEDLINE]

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Select item 229654023.

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. doi: 10.1097/DCR.0b013e31826278b3.

PMID:: 22965402; [PubMed - indexed for MEDLINE]

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Select item 228467384.

Genetic testing by cancer site: stomach.

Chun N, Ford JM.

Cancer J. 2012 Jul-Aug;18(4):355-63. doi: 10.1097/PPO.0b013e31826246dc. Review.

PMID:: 22846738; [PubMed - indexed for MEDLINE]

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Select item 228104755.

The prevalence of hereditary hemorrhagic telangiectasia in juvenile polyposis syndrome.

O'Malley M, LaGuardia L, Kalady MF, Parambil J, Heald B, Eng C, Church J, Burke CA.

Dis Colon Rectum. 2012 Aug;55(8):886-92. doi: 10.1097/DCR.0b013e31825aad32.

PMID:: 22810475; [PubMed - indexed for MEDLINE]

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Select item 227737576.

Reduced bone morphogenetic protein receptor type 1A signaling in neural-crest-derived cells causes facial dysmorphism.

Saito H, Yamamura K, Suzuki N.

Dis Model Mech. 2012 Nov;5(6):948-55. doi: 10.1242/dmm.009274. Epub 2012 Jul 5.

PMID:: 22773757; [PubMed - indexed for MEDLINE]

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Select item 226416937.

Bone morphogenetic proteins differentially regulate pigmentation in human skin cells.

Singh SK, Abbas WA, Tobin DJ.

J Cell Sci. 2012 Sep 15;125(Pt 18):4306-19. doi: 10.1242/jcs.102038. Epub 2012 May 28.

PMID:: 22641693; [PubMed - indexed for MEDLINE]

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Select item 223741478.

Missense mutations of the BMPR1B (ALK6) gene in childhood idiopathic pulmonary arterial hypertension.

Chida A, Shintani M, Nakayama T, Furutani Y, Hayama E, Inai K, Saji T, Nonoyama S, Nakanishi T.

Circ J. 2012;76(6):1501-8. Epub 2012 Feb 25. Erratum in: Circ J. 2012;76(7):1804.

PMID:: 22374147; [PubMed - indexed for MEDLINE]

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Select item 222750019.

Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation.

Tan HL, Glen E, Töpf A, Hall D, O'Sullivan JJ, Sneddon L, Wren C, Avery P, Lewis RJ, ten Dijke P, Arthur HM, Goodship JA, Keavney BD.

Hum Mutat. 2012 Apr;33(4):720-7. doi: 10.1002/humu.22030. Epub 2012 Feb 14.

PMID:: 22275001; [PubMed - indexed for MEDLINE]

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Select item 2225005110.

Identification of TFG (TRK-fused gene) as a putative metastatic melanoma tumor suppressor gene.

Dutton-Regester K, Aoude LG, Nancarrow DJ, Stark MS, O'Connor L, Lanagan C, Pupo GM, Tembe V, Carter CD, O'Rourke M, Scolyer RA, Mann GJ, Schmidt CW, Herington A, Hayward NK.

Genes Chromosomes Cancer. 2012 May;51(5):452-61. doi: 10.1002/gcc.21932. Epub 2012 Jan 17.

PMID:: 22250051; [PubMed - indexed for MEDLINE]

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Select item 2224122011.

The activation of MEK/ERK signaling pathway by bone morphogenetic protein 4 to increase hepatocellular carcinoma cell proliferation and migration.

Chiu CY, Kuo KK, Kuo TL, Lee KT, Cheng KH.

Mol Cancer Res. 2012 Mar;10(3):415-27. doi: 10.1158/1541-7786.MCR-11-0293. Epub 2012 Jan 12.

PMID:: 22241220; [PubMed - indexed for MEDLINE]

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Select item 2217112312.

Juvenile polyposis syndrome.

Brosens LA, Langeveld D, van Hattem WA, Giardiello FM, Offerhaus GJ.

World J Gastroenterol. 2011 Nov 28;17(44):4839-44. doi: 10.3748/wjg.v17.i44.4839. Review.

PMID:: 22171123; [PubMed - indexed for MEDLINE]

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Select item 2206761013.

BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome.

Breckpot J, Tranchevent LC, Thienpont B, Bauters M, Troost E, Gewillig M, Vermeesch JR, Moreau Y, Devriendt K, Van Esch H.

Eur J Med Genet. 2012 Jan;55(1):12-6. doi: 10.1016/j.ejmg.2011.10.003. Epub 2011 Oct 20.

PMID:: 22067610; [PubMed - indexed for MEDLINE]

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Select item 2204875214.

Impacts of age and gender on bone marrow profiles of BMP7, BMPRs and Stro-1⁺ cells in patients with total hip replacement.

Shen Y, Wang W, Li X, Liu Z, Markel DC, Ren W.

Int Orthop. 2012 Apr;36(4):879-86. doi: 10.1007/s00264-011-1370-z. Epub 2011 Nov 3.

PMID:: 22048752; [PubMed - indexed for MEDLINE]

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Select item 2204566615.

PTEN genomic deletions that characterize aggressive prostate cancer originate close to segmental duplications.

Yoshimoto M, Ludkovski O, DeGrace D, Williams JL, Evans A, Sircar K, Bismar TA, Nuin P, Squire JA.

Genes Chromosomes Cancer. 2012 Feb;51(2):149-60. doi: 10.1002/gcc.20939. Epub 2011 Nov 1.

PMID:: 22045666; [PubMed - indexed for MEDLINE]

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Select item 2187288316.

SP1 regulates the transcription of BMPR1A.

Dahdaleh FS, Carr JC, Calva D, Howe JR, Howe JR.

J Surg Res. 2011 Nov;171(1):e15-20. doi: 10.1016/j.jss.2011.06.056. Epub 2011 Jul 23. Erratum in: J Surg Res. 2013 Mar;180(1):183. Howe, James R [added].

PMID:: 21872883; [PubMed - indexed for MEDLINE]

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Select item 2184899417.

Epithelial Bmp (Bone morphogenetic protein) signaling for bulbourethral gland development: a mouse model for congenital cystic dilation.

Omori A, Harada M, Ohta S, Villacorte M, Sugimura Y, Shiraishi T, Suzuki K, Nakagata N, Ito T, Yamada G.

Congenit Anom (Kyoto). 2011 Sep;51(3):102-9. doi: 10.1111/j.1741-4520.2011.00318.x.

PMID:: 21848994; [PubMed - indexed for MEDLINE]

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Select item 2183485818.

Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.

Dahdaleh FS, Carr JC, Calva D, Howe JR.

Clin Genet. 2012 Feb;81(2):110-6. doi: 10.1111/j.1399-0004.2011.01763.x. Epub 2011 Sep 6. Review.

PMID:: 21834858; [PubMed - indexed for MEDLINE]

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Select item 2181161919.

EphB6 receptor modulates micro RNA profile of breast carcinoma cells.

Bhushan L, Kandpal RP.

PLoS One. 2011;6(7):e22484. doi: 10.1371/journal.pone.0022484. Epub 2011 Jul 19.

PMID:: 21811619; [PubMed - indexed for MEDLINE]

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Select item 2180894620.

Interstitial deletion of 10q23.1 and confirmation of three 10qdel syndromes.

Singh S, Aftimos S, George A, Love DR.

Singapore Med J. 2011 Jul;52(7):e143-6.

PMID:: 21808946; [PubMed - indexed for MEDLINE]

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23 free full-text articles in PubMed Central

Reduced bone morphogenetic protein receptor type 1A signaling in neural-crest-derived cells causes facial dysmorphism. [Dis Model Mech. 2012]
Reduced bone morphogenetic protein receptor type 1A signaling in neural-crest-derived cells causes facial dysmorphism.
Saito H, Yamamura K, Suzuki N. Dis Model Mech. 2012 Nov; 5(6):948-55. Epub 2012 Jul 5.
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation. [Hum Mutat. 2012]
Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation.
Tan HL, Glen E, Töpf A, Hall D, O'Sullivan JJ, Sneddon L, Wren C, Avery P, Lewis RJ, ten Dijke P, et al. Hum Mutat. 2012 Apr; 33(4):720-7. Epub 2012 Feb 14.
Review Juvenile polyposis syndrome. [World J Gastroenterol. 2011]
Review Juvenile polyposis syndrome.
Brosens LA, Langeveld D, van Hattem WA, Giardiello FM, Offerhaus GJ. World J Gastroenterol. 2011 Nov 28; 17(44):4839-44.

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