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Items: 1 to 20 of 272

1.
Differential Gene Expression in the Adrenals of Normal and Anencephalic Fetuses and Studies Focused on the Fras-1-Related Extracellular Matrix Protein (FREM2) Gene
Christine W. Mansfield, Bruce R. Carr, Ona M. Faye-Petersen, Dongquan Chen, Yewei Xing, William E. Rainey, C. Richard Parker, Jr
Reprod Sci. 2011 Nov; 18(11): 1146–1153. doi: 10.1177/1933719111408113
PMCID:
PMC3343145
AbstractArticlePDF–292K
2.
Progenitor Cell Line (hPheo1) Derived from a Human Pheochromocytoma Tumor
Hans K. Ghayee, Vikash J. Bhagwandin, Victor Stastny, Arielle Click, Liang-Hao Ding, Dario Mizrachi, Ying S. Zou, Raj Chari, Wan L. Lam, Robert M. Bachoo, Alice L. Smith, Michael D. Story, Stan Sidhu, Bruce G. Robinson, Fiemu E. Nwariaku, Adi F. Gazdar, Richard J. Auchus, Jerry W. Shay
PLoS One. 2013; 8(6): e65624. Published online 2013 Jun 13. doi: 10.1371/journal.pone.0065624
PMCID:
PMC3681983
AbstractArticlePDF–751K
3.
Mitochondrial tRNAPhe mutation as a cause of end-stage renal disease in childhood
Kristin E D’Aco, Megan Manno, Colleen Clarke, Jaya Ganesh, Kevin EC Meyers, Neal Sondheimer
Pediatr Nephrol. Author manuscript; available in PMC 2014 Mar 1.
Published in final edited form as: Pediatr Nephrol. 2013 Mar; 28(3): 515–519. Published online 2012 Nov 8. doi: 10.1007/s00467-012-2354-y
PMCID:
PMC3557766
AbstractArticlePDF–851K
4.
Macrophage SR-BI regulates LPS-induced pro-inflammatory signaling in mice and isolated macrophages
Lei Cai, Zhen Wang, Jason M. Meyer, Ailing Ji, Deneys R. van der Westhuyzen
J Lipid Res. 2012 Aug; 53(8): 1472–1481. doi: 10.1194/jlr.M023234
PMCID:
PMC3540840
AbstractArticlePDF–1.2M
5.
Insulin and IGF1 Receptors Are Essential for XX and XY Gonadal Differentiation and Adrenal Development in Mice
Jean-Luc Pitetti, Pierre Calvel, Yannick Romero, Béatrice Conne, Vy Truong, Marilena D. Papaioannou, Olivier Schaad, Mylène Docquier, Pedro Luis Herrera, Dagmar Wilhelm, Serge Nef
PLoS Genet. 2013 Jan; 9(1): e1003160. Published online 2013 Jan 3. doi: 10.1371/journal.pgen.1003160
PMCID:
PMC3536656
AbstractArticlePDF–9.4M
6.
A Novel Missense Mutation in Dax-1 with an Unusual Presentation of X-Linked Adrenal Hypoplasia Congenita
Imran Ahmad, Wendy F. Paterson, Lin Lin, Peter Adlard, Philippa Duncan, John Tolmie, John C. Achermann, Malcolm D.C. Donaldson
Horm Res. Author manuscript; available in PMC 2012 Oct 23.
Published in final edited form as: Horm Res. 2007; 68(1): 32–37. Published online 2007 Feb 16. doi: 10.1159/000099835
PMCID:
PMC3479083
AbstractArticlePDF–331K
7.
Functional Significance of SRJ Domain Mutations in CITED2
Chiann-mun Chen, Jamie Bentham, Catherine Cosgrove, Jose Braganca, Ana Cuenda, Simon D. Bamforth, Jürgen E. Schneider, Hugh Watkins, Bernard Keavney, Benjamin Davies, Shoumo Bhattacharya
PLoS One. 2012; 7(10): e46256. Published online 2012 Oct 17. doi: 10.1371/journal.pone.0046256
PMCID:
PMC3474824
AbstractArticlePDF–853K
8.
Neuroimmunoendocrine Regulation of the Prion Protein in Neutrophils
Rafael M. Mariante, Alberto Nóbrega, Rodrigo A. P. Martins, Rômulo B. Areal, Maria Bellio, Rafael Linden
J Biol Chem. 2012 Oct 12; 287(42): 35506–35515. Published online 2012 Aug 21. doi: 10.1074/jbc.M112.394924
PMCID:
PMC3471762
AbstractArticlePDF–2.4M
9.
Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
Radha Nandagopal, Ninet Sinaii, Nilo A Avila, Carol Van Ryzin, Wuyan Chen, Gabriela P Finkielstain, Sneha P Mehta, Nazli B McDonnel, Deborah P Merke
Eur J Endocrinol. Author manuscript; available in PMC 2012 Oct 15.
Published in final edited form as: Eur J Endocrinol. 2011 Jun; 164(6): 977–984. Published online 2011 Mar 28. doi: 10.1530/EJE-11-0019
PMCID:
PMC3470911
AbstractArticlePDF–360K
10.
Massive Neonatal Adrenal Enlargement Due to Cytomegaly, Persistence of the Transient Cortex, and Hyperplasia of the Permanent Cortex: Findings in Cushing Syndrome Associated With Hemihypertrophy
J. Aidan Carney, Josephine Ho, Kazuteru Kitsuda, William F. Young, Jr, Constantine A. Stratakis
Am J Surg Pathol. Author manuscript; available in PMC 2013 Oct 1.
Published in final edited form as: Am J Surg Pathol. 2012 Oct; 36(10): 1452–1463. doi: 10.1097/PAS.0b013e31825d538b
PMCID:
PMC3444746
AbstractArticlePDF–6.3M
11.
Progression to Adrenocortical Tumorigenesis in Mice and Humans through Insulin-Like Growth Factor 2 and β-Catenin
Joanne H. Heaton, Michelle A. Wood, Alex C. Kim, Lorena O. Lima, Ferdous M. Barlaskar, Madson Q. Almeida, Maria C.B.V. Fragoso, Rork Kuick, Antonio M. Lerario, Derek P. Simon, Ibere C. Soares, Elisabeth Starnes, Dafydd G. Thomas, Ana C. Latronico, Thomas J. Giordano, Gary D. Hammer
Am J Pathol. 2012 Sep; 181(3): 1017–1033. doi: 10.1016/j.ajpath.2012.05.026
PMCID:
PMC3432433
AbstractArticlePDF–2.7M
12.
Autonomic neurocristopathy-associated mutations in PHOX2B dysregulate Sox10 expression
Mayumi Nagashimada, Hiroshi Ohta, Chong Li, Kazuki Nakao, Toshihiro Uesaka, Jean-François Brunet, Jeanne Amiel, Delphine Trochet, Teruhiko Wakayama, Hideki Enomoto
J Clin Invest. 2012 Sep 4; 122(9): 3145–3158. Published online 2012 Aug 27. doi: 10.1172/JCI63401
PMCID:
PMC3428093
AbstractArticlePDF–6.9M
13.
Biomarkers of hypothalamic–pituitary–adrenal axis activity in mice lacking 11β-HSD1 and H6PDH
Lianne Abrahams, Nina M Semjonous, Phil Guest, Agnieszka Zielinska, Beverly Hughes, Gareth G Lavery, Paul M Stewart
J Endocrinol. 2012 Sep; 214(3): 367–372. Prepublished online 2012 Jun 20. doi: 10.1530/JOE-12-0178
PMCID:
PMC3427643
AbstractArticlePDF–171K
14.
Pax7 Lineage Contributions to the Mammalian Neural Crest
Barbara Murdoch, Casey DelConte, Martín I. García-Castro
PLoS One. 2012; 7(7): e41089. Published online 2012 Jul 27. doi: 10.1371/journal.pone.0041089
PMCID:
PMC3407174
AbstractArticlePDF–8.1M
15.
Ablation of Vimentin Results in Defective Steroidogenesis
Wen-Jun Shen, Syed Kashif Zaidi, Shailja Patel, Yuan Cortez, Masami Ueno, Rakia Azhar, Salman Azhar, Fredric B. Kraemer
Endocrinology. 2012 Jul; 153(7): 3249–3257. Published online 2012 Apr 24. doi: 10.1210/en.2012-1048
PMCID:
PMC3380307
AbstractArticle
16.
Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency
Nils Krone, Nicole Reisch, Jan Idkowiak, Vivek Dhir, Hannah E. Ivison, Beverly A. Hughes, Ian T. Rose, Donna M. O'Neil, Raymon Vijzelaar, Matthew J. Smith, Fiona MacDonald, Trevor R. Cole, Nicolai Adolphs, John S. Barton, Edward M. Blair, Stephen R. Braddock, Felicity Collins, Deborah L. Cragun, Mehul T. Dattani, Ruth Day, Shelley Dougan, Miriam Feist, Michael E. Gottschalk, John W. Gregory, Michaela Haim, Rachel Harrison, Ann Haskins Olney, Berthold P. Hauffa, Peter C. Hindmarsh, Robert J. Hopkin, Petr E. Jira, Marlies Kempers, Michiel N. Kerstens, Mohamed M. Khalifa, Birgit Köhler, Dominique Maiter, Shelly Nielsen, Stephen M. O'Riordan, Christian L. Roth, Kate P. Shane, Martin Silink, Nike M. M. L. Stikkelbroeck, Elizabeth Sweeney, Maria Szarras-Czapnik, John R. Waterson, Lori Williamson, Michaela F. Hartmann, Norman F. Taylor, Stefan A. Wudy, Ewa M. Malunowicz, Cedric H. L. Shackleton, Wiebke Arlt
J Clin Endocrinol Metab. 2012 Feb; 97(2): E257–E267. Published online 2011 Dec 7. doi: 10.1210/jc.2011-0640
PMCID:
PMC3380101
AbstractArticle
17.
Hypoxia-Inducible Factor Signaling in Pheochromocytoma: Turning the Rudder in the Right Direction
Ivana Jochmanová, Chunzhang Yang, Zhengping Zhuang, Karel Pacak
J Natl Cancer Inst. 2013 Sep 4; 105(17): 1270–1283. Published online 2013 Aug 12. doi: 10.1093/jnci/djt201
PMCID:
PMC3888279
AbstractArticlePDF–7.1M
18.
Potassium Channel Mutant KCNJ5 T158A Expression in HAC-15 Cells Increases Aldosterone Synthesis
Kenji Oki, Maria W. Plonczynski, Milay Luis Lam, Elise P. Gomez-Sanchez, Celso E. Gomez-Sanchez
Endocrinology. 2012 Apr; 153(4): 1774–1782. Published online 2012 Feb 7. doi: 10.1210/en.2011-1733
PMCID:
PMC3320257
AbstractArticle
19.
Activation of Cyclic AMP Signaling Leads to Different Pathway Alterations in Lesions of the Adrenal Cortex Caused by Germline PRKAR1A Defects versus Those due to Somatic GNAS Mutations
Madson Q. Almeida, Monalisa F. Azevedo, Paraskevi Xekouki, Eirini I. Bimpaki, Anelia Horvath, Michael T. Collins, Lefkothea P. Karaviti, George S. Jeha, Nisan Bhattacharyya, Chris Cheadle, Tonya Watkins, Isabelle Bourdeau, Maria Nesterova, Constantine A. Stratakis
J Clin Endocrinol Metab. 2012 Apr; 97(4): E687–E693. Published online 2012 Jan 18. doi: 10.1210/jc.2011-3000
PMCID:
PMC3319183
AbstractArticle
20.
Microcephaly, Intellectual Impairment, Bilateral Vesicoureteral Reflux, Distichiasis and Glomuvenous Malformations Associated with a 16q24.3 Contiguous Gene Deletion and a Glomulin Mutation
Matthew G. Butler, Susan L. Dagenais, José L. Garcia-Perez, Pascal Brouillard, Miikka Vikkula, Peter Strouse, Jeffrey W. Innis, Thomas W. Glover
Am J Med Genet A. Author manuscript; available in PMC 2013 Apr 1.
Published in final edited form as: Am J Med Genet A. 2012 Apr; 158A(4): 839–849. Published online 2012 Mar 9. doi: 10.1002/ajmg.a.35229
PMCID:
PMC3314153
AbstractArticlePDF–2.1M

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