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Items: 1 to 20 of 23


Genetics of Adrenocortical Development and Tumors.

Lodish M.

Endocrinol Metab Clin North Am. 2017 Jun;46(2):419-433. doi: 10.1016/j.ecl.2017.01.007. Epub 2017 Feb 22. Review.


Association of WNT4 polymorphisms with endometriosis in infertile patients.

Mafra F, Catto M, Bianco B, Barbosa CP, Christofolini D.

J Assist Reprod Genet. 2015 Sep;32(9):1359-64. doi: 10.1007/s10815-015-0523-1. Epub 2015 Jul 3.


Fetal adrenal capsular cells serve as progenitor cells for steroidogenic and stromal adrenocortical cell lineages in M. musculus.

Wood MA, Acharya A, Finco I, Swonger JM, Elston MJ, Tallquist MD, Hammer GD.

Development. 2013 Nov;140(22):4522-32. doi: 10.1242/dev.092775. Epub 2013 Oct 16.


Investigating the role of adrenal cortex in organization and differentiation of the adrenal medulla in mice.

Huang CC, Liu C, Yao HH.

Mol Cell Endocrinol. 2012 Sep 25;361(1-2):165-71. doi: 10.1016/j.mce.2012.04.004. Epub 2012 May 3.


Adrenocortical stem and progenitor cells: implications for adrenocortical carcinoma.

Simon DP, Hammer GD.

Mol Cell Endocrinol. 2012 Mar 31;351(1):2-11. doi: 10.1016/j.mce.2011.12.006. Epub 2012 Jan 13. Review.


Animal models of adrenocortical tumorigenesis.

Beuschlein F, Galac S, Wilson DB.

Mol Cell Endocrinol. 2012 Mar 31;351(1):78-86. doi: 10.1016/j.mce.2011.09.045. Epub 2011 Nov 11.


Sonic hedgehog signaling during adrenal development.

Laufer E, Kesper D, Vortkamp A, King P.

Mol Cell Endocrinol. 2012 Mar 31;351(1):19-27. doi: 10.1016/j.mce.2011.10.002. Epub 2011 Oct 13. Review.


Evidence of adrenal failure in aging Dax1-deficient mice.

Scheys JO, Heaton JH, Hammer GD.

Endocrinology. 2011 Sep;152(9):3430-9. doi: 10.1210/en.2010-0986. Epub 2011 Jul 5.


Adrenocortical stem and progenitor cells: unifying model of two proposed origins.

Wood MA, Hammer GD.

Mol Cell Endocrinol. 2011 Apr 10;336(1-2):206-12. doi: 10.1016/j.mce.2010.11.012. Epub 2010 Nov 20. Review.


Development and function of the human fetal adrenal cortex: a key component in the feto-placental unit.

Ishimoto H, Jaffe RB.

Endocr Rev. 2011 Jun;32(3):317-55. doi: 10.1210/er.2010-0001. Epub 2010 Nov 4. Review.


The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders.

Miller WL, Auchus RJ.

Endocr Rev. 2011 Feb;32(1):81-151. doi: 10.1210/er.2010-0013. Epub 2010 Nov 4. Review. Erratum in: Endocr Rev. 2011 Aug;32(4):579.


Angiotensin II-regulated transcription regulatory genes in adrenal steroidogenesis.

Romero DG, Gomez-Sanchez EP, Gomez-Sanchez CE.

Physiol Genomics. 2010 Nov 29;42A(4):259-66. doi: 10.1152/physiolgenomics.00098.2010. Epub 2010 Sep 28.


Differences in aggressive behavior and DNA copy number variants between BALB/cJ and BALB/cByJ substrains.

Velez L, Sokoloff G, Miczek KA, Palmer AA, Dulawa SC.

Behav Genet. 2010 Mar;40(2):201-10. doi: 10.1007/s10519-009-9325-5. Epub 2009 Dec 23.


Shh signaling regulates adrenocortical development and identifies progenitors of steroidogenic lineages.

King P, Paul A, Laufer E.

Proc Natl Acad Sci U S A. 2009 Dec 15;106(50):21185-90. doi: 10.1073/pnas.0909471106. Epub 2009 Dec 1.


Genetic p53 deficiency partially rescues the adrenocortical dysplasia phenotype at the expense of increased tumorigenesis.

Else T, Trovato A, Kim AC, Wu Y, Ferguson DO, Kuick RD, Lucas PC, Hammer GD.

Cancer Cell. 2009 Jun 2;15(6):465-76. doi: 10.1016/j.ccr.2009.04.011.


In search of adrenocortical stem and progenitor cells.

Kim AC, Barlaskar FM, Heaton JH, Else T, Kelly VR, Krill KT, Scheys JO, Simon DP, Trovato A, Yang WH, Hammer GD.

Endocr Rev. 2009 May;30(3):241-63. doi: 10.1210/er.2008-0039. Epub 2009 Apr 29. Review.


Review paper: origin and molecular pathology of adrenocortical neoplasms.

Bielinska M, Parviainen H, Kiiveri S, Heikinheimo M, Wilson DB.

Vet Pathol. 2009 Mar;46(2):194-210. doi: 10.1354/vp.46-2-194. Review.


CBP/p300-interacting transactivator, with Glu/Asp-rich C-terminal domain, 2, and pre-B-cell leukemia transcription factor 1 in human adrenal development and disease.

Ferraz-de-Souza B, Martin F, Mallet D, Hudson-Davies RE, Cogram P, Lin L, Gerrelli D, Beuschlein F, Morel Y, Huebner A, Achermann JC.

J Clin Endocrinol Metab. 2009 Feb;94(2):678-83. doi: 10.1210/jc.2008-1064. Epub 2008 Nov 4.


SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4.

Mandel H, Shemer R, Borochowitz ZU, Okopnik M, Knopf C, Indelman M, Drugan A, Tiosano D, Gershoni-Baruch R, Choder M, Sprecher E.

Am J Hum Genet. 2008 Jan;82(1):39-47. doi: 10.1016/j.ajhg.2007.08.005.

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