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Items: 1 to 20 of 214


Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect.

Bhatti TR, Ganapathy K, Huppmann AR, Conlin L, Boodhansingh KE, MacMullen C, Becker S, Ernst LM, Adzick NS, Ruchelli ED, Ganguly A, Stanley CA.

J Clin Endocrinol Metab. 2016 Mar;101(3):914-22. doi: 10.1210/jc.2015-2914. Epub 2016 Jan 12.


The Cell Death Inhibitor ARC Is Induced in a Tissue-Specific Manner by Deletion of the Tumor Suppressor Gene Men1, but Not Required for Tumor Development and Growth.

McKimpson WM, Yuan Z, Zheng M, Crabtree JS, Libutti SK, Kitsis RN.

PLoS One. 2015 Dec 28;10(12):e0145792. doi: 10.1371/journal.pone.0145792. eCollection 2015.


Familial syndromes associated with neuroendocrine tumours.

Gut P, Komarowska H, Czarnywojtek A, Waligórska-Stachura J, Bączyk M, Ziemnicka K, Fischbach J, Wrotkowska E, Ruchała M.

Contemp Oncol (Pozn). 2015;19(3):176-83. doi: 10.5114/wo.2015.52710. Epub 2015 Jul 8. Review.


A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma.

Remde H, Kaminsky E, Werner M, Quinkler M.

Endocrinol Diabetes Metab Case Rep. 2015;2015. pii: 14-0120. doi: 10.1530/EDM-14-0120. Epub 2015 Feb 25.


Novel MEN 1 gene findings in rare sporadic insulinoma--a case control study.

Jyotsna VP, Malik E, Birla S, Sharma A.

BMC Endocr Disord. 2015 Aug 26;15:44. doi: 10.1186/s12902-015-0041-2.


Introduction of Francis S. Collins.

Ginsburg D.

J Clin Invest. 2015 Sep;125(9):3321-7. doi: 10.1172/JCI83698. Epub 2015 Aug 17. No abstract available.


Consequence of Menin Deficiency in Mouse Adipocytes Derived by In Vitro Differentiation.

Parekh VI, Modali SD, Desai SS, Agarwal SK.

Int J Endocrinol. 2015;2015:149826. doi: 10.1155/2015/149826. Epub 2015 Jul 2.


The molecular classification of hereditary endocrine diseases.

Ye L, Ning G.

Endocrine. 2015 Dec;50(3):575-9. doi: 10.1007/s12020-015-0674-y. Epub 2015 Jul 7.


Roles of DPY30 in the Proliferation and Motility of Gastric Cancer Cells.

Lee YJ, Han ME, Baek SJ, Kim SY, Oh SO.

PLoS One. 2015 Jul 6;10(7):e0131863. doi: 10.1371/journal.pone.0131863. eCollection 2015.


EPMA position paper in cancer: current overview and future perspectives.

Grech G, Zhan X, Yoo BC, Bubnov R, Hagan S, Danesi R, Vittadini G, Desiderio DM.

EPMA J. 2015 Apr 15;6(1):9. doi: 10.1186/s13167-015-0030-6. eCollection 2015.


Laser capture microdissection: Big data from small samples.

Datta S, Malhotra L, Dickerson R, Chaffee S, Sen CK, Roy S.

Histol Histopathol. 2015 Nov;30(11):1255-69. doi: 10.14670/HH-11-622. Epub 2015 Apr 20. Review.


Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1.

Circelli L, Ramundo V, Marotta V, Sciammarella C, Marciello F, Del Prete M, Sabatino L, Pasquali D, Izzo F, Scala S, Colao A, Faggiano A, Colantuoni V; Multidisciplinary Group for NeuroEndocrine Tumours of Naples.

J Cell Mol Med. 2015 Jul;19(7):1735-41. doi: 10.1111/jcmm.12552. Epub 2015 Mar 30.


Targeting the MLL complex in castration-resistant prostate cancer.

Malik R, Khan AP, Asangani IA, Cieślik M, Prensner JR, Wang X, Iyer MK, Jiang X, Borkin D, Escara-Wilke J, Stender R, Wu YM, Niknafs YS, Jing X, Qiao Y, Palanisamy N, Kunju LP, Krishnamurthy PM, Yocum AK, Mellacheruvu D, Nesvizhskii AI, Cao X, Dhanasekaran SM, Feng FY, Grembecka J, Cierpicki T, Chinnaiyan AM.

Nat Med. 2015 Apr;21(4):344-52. doi: 10.1038/nm.3830. Epub 2015 Mar 30.


Neomorphic effects of recurrent somatic mutations in Yin Yang 1 in insulin-producing adenomas.

Cromer MK, Choi M, Nelson-Williams C, Fonseca AL, Kunstman JW, Korah RM, Overton JD, Mane S, Kenney B, Malchoff CD, Stalberg P, Akerström G, Westin G, Hellman P, Carling T, Björklund P, Lifton RP.

Proc Natl Acad Sci U S A. 2015 Mar 31;112(13):4062-7. doi: 10.1073/pnas.1503696112. Epub 2015 Mar 18.


Genetic analysis of a patient with coexisting acromegaly, thyroid papillary carcinoma and subcutaneous fibroma.

Liu J, Tang X, Cheng J, Wang L, Yang X, Wang Y.

Oncol Lett. 2015 Mar;9(3):1177-1180. Epub 2014 Dec 23.


Tumour nuclear oestrogen receptor beta 1 correlates inversely with parathyroid tumour weight.

Haglund F, Rosin G, Nilsson IL, Juhlin CC, Pernow Y, Norenstedt S, Dinets A, Larsson C, Hartman J, Höög A.

Endocr Connect. 2015 Mar;4(1):76-85. doi: 10.1530/EC-14-0109. Epub 2015 Feb 3.


MEN1 mutations in Hürthle cell (oncocytic) thyroid carcinoma.

Kasaian K, Chindris AM, Wiseman SM, Mungall KL, Zeng T, Tse K, Schein JE, Rivera M, Necela BM, Kachergus JM, Casler JD, Mungall AJ, Moore RA, Marra MA, Copland JA, Thompson EA, Smallridge RC, Jones SJ.

J Clin Endocrinol Metab. 2015 Apr;100(4):E611-5. doi: 10.1210/jc.2014-3622. Epub 2015 Jan 27.


Recurrent ZFX mutations in human sporadic parathyroid adenomas.

Soong CP, Arnold A.

Oncoscience. 2014 May 6;1(5):360-6. eCollection 2014. Erratum in: Oncoscience. 2015;2(1):1-2.

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