Pathogenesis of Corticotropic Tumors
暂无分享,去创建一个
[1] J. Bertherat,et al. Cushing's disease. , 2009, Best practice & research. Clinical endocrinology & metabolism.
[2] B. Meij,et al. Cushing’s Disease in Dogs and Humans , 2009, Hormone Research in Paediatrics.
[3] M. Malumbres,et al. Cell cycle control of pituitary development and disease. , 2008, Journal of molecular endocrinology.
[4] A. Grossman,et al. Are neuroendocrine tumours a feature of tuberous sclerosis? A systematic review. , 2008, Endocrine-related cancer.
[5] K. Kovacs,et al. p21Cip1 restrains pituitary tumor growth , 2008, Proceedings of the National Academy of Sciences.
[6] J. Drouin,et al. Regulatory Network Analyses Reveal Genome-Wide Potentiation of LIF Signaling by Glucocorticoids and Define an Innate Cell Defense Response , 2008, PLoS genetics.
[7] K. Kovacs,et al. Senescence mediates pituitary hypoplasia and restrains pituitary tumor growth. , 2007, Cancer research.
[8] S. Bilodeau,et al. Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiency , 2007, Clinical genetics.
[9] S. Melmed,et al. Pituitary tumor-transforming gene: physiology and implications for tumorigenesis. , 2007, Endocrine reviews.
[10] Michael Buchfelder,et al. Pathohistological classification of pituitary tumors: 10 years of experience with the German Pituitary Tumor Registry. , 2007, European journal of endocrinology.
[11] J. Bertherat,et al. Corticotroph tumor progression after adrenalectomy in Cushing's Disease: A reappraisal of Nelson's Syndrome. , 2007, The Journal of clinical endocrinology and metabolism.
[12] D. Figarella-Branger,et al. Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease. , 2006, Genes & development.
[13] K. Kovacs,et al. Pituitary hypoplasia in Pttg-/- mice is protective for Rb+/- pituitary tumorigenesis. , 2005, Molecular endocrinology.
[14] G. Camerino,et al. Corticotroph adenoma of the pituitary in a patient with X-linked adrenal hypoplasia congenita due to a novel mutation of the DAX-1 gene. , 2005, European journal of endocrinology.
[15] J. Bertherat,et al. The Nelson's syndrome... revisited , 2005, Pituitary.
[16] S. Asa,et al. The 2004 World Health Organization classification of pituitary tumors: What is new? , 2005, Acta Neuropathologica.
[17] R. Bronson,et al. A dynamic switch in Rb+/− mediated neuroendocrine tumorigenesis , 2004, Oncogene.
[18] C. A. Blake,et al. Effects of corticotrophin-releasing hormone on corticotrophs in anterior pituitary gland allografts in hypophysectomized, orchidectomized hamsters , 1989, Cell and Tissue Research.
[19] R. DeLellis. Pathology and genetics of tumours of endocrine organs , 2004 .
[20] S. Czirják,et al. Identification of adrenocorticotropin receptor messenger ribonucleic acid in the human pituitary and its loss of expression in pituitary adenomas. , 2003, The Journal of clinical endocrinology and metabolism.
[21] S. Melmed. Mechanisms for pituitary tumorigenesis: the plastic pituitary. , 2003, The Journal of clinical investigation.
[22] B. Scheithauer,et al. Crooke's Cell Adenoma of the Pituitary: An Aggressive Variant of Corticotroph Adenoma , 2003, The American journal of surgical pathology.
[23] X. Bertagna,et al. Proopiomelanocortin, a polypeptide precursor with multiple functions: from physiology to pathological conditions. , 2003, European journal of endocrinology.
[24] Joseph B. Rayman,et al. E2F4 loss suppresses tumorigenesis in Rb mutant mice. , 2002, Cancer cell.
[25] X. Bertagna,et al. Overexpression of the V3 Vasopressin Receptor in Transgenic Mice Corticotropes Leads to Increased Basal Corticosterone , 2002, Journal of neuroendocrinology.
[26] G. Sassolas,et al. Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. , 2002, The Journal of clinical endocrinology and metabolism.
[27] E. Berg,et al. World Health Organization Classification of Tumours , 2002 .
[28] V. Godfrey,et al. Functional Collaboration between Different Cyclin-Dependent Kinase Inhibitors Suppresses Tumor Growth with Distinct Tissue Specificity , 2000, Molecular and Cellular Biology.
[29] S. Melmed,et al. Leukemia-inhibitory factor-neuroimmune modulator of endocrine function. , 2000, Endocrine reviews.
[30] J. Doppman,et al. Extrapituitary parasellar microadenoma in Cushing's disease. , 1999, The Journal of clinical endocrinology and metabolism.
[31] C. Cordon-Cardo,et al. p27 and Rb are on overlapping pathways suppressing tumorigenesis in mice. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[32] R. Fahlbusch,et al. Expression of menin gene mRNA in pituitary tumours. , 1999, European journal of endocrinology.
[33] P. Dahia,et al. The molecular pathogenesis of corticotroph tumors. , 1999, Endocrine reviews.
[34] J. Rutka,et al. Molecular Pathogenesis of Pituitary Adenomas: A Review , 1999, Acta Neurochirurgica.
[35] C. Readhead,et al. Pituitary-directed leukemia inhibitory factor transgene causes Cushing's syndrome: neuro-immune-endocrine modulation of pituitary development. , 1998, Molecular endocrinology.
[36] V. Godfrey,et al. CDK inhibitors p18(INK4c) and p27(Kip1) mediate two separate pathways to collaboratively suppress pituitary tumorigenesis. , 1998, Genes & development.
[37] E. Gundelfinger,et al. Mutation and expression analysis of corticotropin-releasing factor 1 receptor in adrenocorticotropin-secreting pituitary adenomas. , 1998, The Journal of clinical endocrinology and metabolism.
[38] S. Asa,et al. The MEN-1 gene is rarely down-regulated in pituitary adenomas. , 1998, The Journal of clinical endocrinology and metabolism.
[39] T. Jacks,et al. p21 Is a Critical CDK2 Regulator Essential for Proliferation Control in Rb-deficient Cells , 1998, The Journal of cell biology.
[40] T. Jacks,et al. Loss of E2F-1 reduces tumorigenesis and extends the lifespan of Rb1(+/−) mice , 1998, Nature Genetics.
[41] S. Lamberts,et al. Human adrenocorticotropin-secreting pituitary adenomas show frequent loss of heterozygosity at the glucocorticoid receptor gene locus. , 1998, The Journal of clinical endocrinology and metabolism.
[42] D. Grobbee,et al. A polymorphism in the glucocorticoid receptor gene may be associated with and increased sensitivity to glucocorticoids in vivo. , 1998, The Journal of clinical endocrinology and metabolism.
[43] R. Fahlbusch,et al. Journal of Clinical Endocrinology and Metabolism Printed in U.S.A. Copyright © 1997 by The Endocrine Society Expression of Glucocorticoid Receptor Gene Isoforms in Corticotropin-Secreting Tumors* , 2022 .
[44] Nobuyuki Shishido,et al. Mice Lacking p27 Kip1 Display Increased Body Size, Multiple Organ Hyperplasia, Retinal Dysplasia, and Pituitary Tumors , 1996, Cell.
[45] James M. Roberts,et al. A Syndrome of Multiorgan Hyperplasia with Features of Gigantism, Tumorigenesis, and Female Sterility in p27 Kip1 -Deficient Mice , 1996, Cell.
[46] K. Manova-Todorova,et al. Enhanced Growth of Mice Lacking the Cyclin-Dependent Kinase Inhibitor Function of p27 Kip1 , 1996, Cell.
[47] R. Fahlbusch,et al. Vasopressin receptor expression and mutation analysis in corticotropin-secreting tumors. , 1996, The Journal of clinical endocrinology and metabolism.
[48] T. Mindermann,et al. Age‐related and gender‐related occurrence of pituitary adenomas , 1994, Clinical endocrinology.
[49] R. G. Allen,et al. Post-translational processing of proopiomelanocortin (POMC) in mouse pituitary melanotroph tumors induced by a POMC-simian virus 40 large T antigen transgene. , 1993, The Journal of biological chemistry.
[50] K. Kovacs. The pathology of cushing's disease , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[51] X. Bertagna. Unrestrained production of proopiomelanocortin (POMC) and its peptide fragments by pituitary corticotroph adenomas in Cushing's disease , 1992, The Journal of Steroid Biochemistry and Molecular Biology.
[52] A. Berns,et al. Requirement for a functional Rb-1 gene in murine development , 1992, Nature.
[53] R. Weinberg,et al. Effects of an Rb mutation in the mouse , 1992, Nature.
[54] A. Bradley,et al. Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesis , 1992, Nature.
[55] J. Vaughan,et al. Development of Cushing's syndrome in corticotropin-releasing factor transgenic mice. , 1992, Endocrinology.
[56] G. Siegal,et al. Transgenic mice that develop pituitary tumors. A model for Cushing's disease. , 1992, The American journal of pathology.
[57] K. Kovacs,et al. Clonal origin of pituitary adenomas. , 1990, The Journal of clinical endocrinology and metabolism.
[58] A. Arnold,et al. Clinically nonfunctioning pituitary tumors are monoclonal in origin. , 1990, The Journal of clinical investigation.
[59] B. Scheithauer,et al. Tumors of the Pituitary Gland , 1990 .
[60] T. Suda,et al. Effects of corticotropin-releasing hormone and dexamethasone on proopiomelanocortin messenger RNA level in human corticotroph adenoma cells in vitro. , 1988, The Journal of clinical investigation.
[61] D. Hanahan,et al. Endothelial cell tumors develop in transgenic mice carrying polyoma virus middle T oncogene , 1987, Cell.
[62] K. Kovacs,et al. Chronic administration of corticotropin-releasing factor increases pituitary corticotroph number. , 1987, Endocrinology.
[63] X. Bertagna,et al. Altered proopiomelanocortin gene expression in adrenocorticotropin-producing nonpituitary tumors. Comparative studies with corticotropic adenomas and normal pituitaries. , 1985, The Journal of clinical investigation.
[64] R. Fahlbusch,et al. OVINE CORTICOTROPHIN RELEASING FACTOR STIMULATES ACTH RELEASE FROM HUMAN CORTICOTROPHINOMA CELLS IN CULTURE; INTERACTION WITH HYDROCORTISONE AND ARGININE VASOPRESSIN , 1985, Clinical endocrinology.
[65] V. Challa,et al. Pathobiologic study of pituitary tumors: report of 62 cases with a review of the recent literature. , 1985, Human pathology.
[66] W. Burch. Cushing's disease. A review. , 1985, Archives of internal medicine.
[67] S. Lamberts,et al. Studies on the glucocorticoid-receptor blocking action of RU 38486 in cultured ACTH-secreting human pituitary tumour cells and normal rat pituitary cells. , 1985, Acta endocrinologica.
[68] K. Westlund,et al. Quantification of morphological changes in pituitary corticotropes produced by in vivo corticotropin-releasing factor stimulation and adrenalectomy. , 1985, Endocrinology.
[69] S. Lamberts,et al. ACTH and beta-endorphin secretion by three corticotrophic adenomas in culture. Effects of culture time, dexamethasone, vasopressin and synthetic corticotrophin releasing factor. , 1984, Acta endocrinologica.
[70] W. Vale,et al. Pituitary microadenomas causing Cushing's disease respond to corticotropin-releasing factor. , 1982, The Journal of clinical endocrinology and metabolism.
[71] W. Nicholson,et al. Equine Cushing's disease: plasma immunoreactive proopiolipomelanocortin peptide and cortisol levels basally and in response to diagnostic tests. , 1982, Endocrinology.
[72] W. Nicholson,et al. Proopiolipomelanocortin peptides in normal pituitary, pituitary tumor, and plasma of normal and Cushing's horses. , 1982, Endocrinology.
[73] W. Priester,et al. Epidemiological aspects of clinical hyperadrenocorticism in dogs (canine Cushing's syndrome). , 1982 .
[74] D. Krieger,et al. Pituitary intermediate lobe in dog: two cell types and high bioactive adrenocorticotropin content. , 1981, Science.
[75] A. Grossman,et al. SECRETION OF ACTH, LPH AND β‐ENDORPHIN FROM HUMAN PITUITARY TUMOURS IN VITRO , 1980 .
[76] G. Gillies,et al. Adrenocorticotropin and lipotropin secretion by dispersed cell cultures of a human corticotropic adenoma: effect of hypothalamic extract, arginine vasopressin, hydrocortisone, and serotonin. , 1980, The Journal of clinical endocrinology and metabolism.
[77] J. Klijn,et al. The mechanism of the suppressive action of bromocriptine on adrenocorticotropin secretion in patients with Cushing's disease and Nelson's syndrome. , 1980, The Journal of clinical endocrinology and metabolism.
[78] W. Odell,et al. THE DOSE‐RESPONSE RELATIONSHIP OF ACTH AND CORTISOL IN CUSHING'S DISEASE , 1980, Clinical endocrinology.
[79] S. Lamberts,et al. Failure of clinical remission after transsphenoidal removal of a microadenoma in a patient with Cushing's disease: multiple hyperplastic and adenomatous cell nets in surrounding pituitary tissue. , 1980, The Journal of clinical endocrinology and metabolism.