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reverse transcriptase polymerase chain reaction (5) 5
signal transduction - drug effects (5) 5
somatostatin (5) 5
ubiquitin thiolesterase - genetics (5) 5
acth-secreting pituitary adenoma - genetics (4) 4
adolescent (4) 4
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pituitary acth hypersecretion - genetics (4) 4
pituitary gland - pathology (4) 4
pituitary neoplasms - complications (4) 4
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pro-opiomelanocortin - genetics (4) 4
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cercopithecus aethiops (3) 3
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1. Full Text Mutations in the deubiquitinase gene USP8 cause Cushing's disease
by Reincke, Martin and Sbiera, Silviu and Hayakawa, Akira and Theodoropoulou, Marily and Osswald, Andrea and Beuschlein, Felix and Meitinger, Thomas and Mizuno-Yamasaki, Emi and Kawaguchi, Kohei and Saeki, Yasushi and Tanaka, Keiji and Wieland, Thomas and Graf, Elisabeth and Saeger, Wolfgang and Ronchi, Cristina L and Allolio, Bruno and Buchfelder, Michael and Strom, Tim M and Fassnacht, Martin and Komada, Masayuki
Nature Genetics, ISSN 1061-4036, 12/2014, Volume 47, Issue 1, pp. 31 - 38
Cushing's disease is caused by corticotroph adenomas of the pituitary. To explore the molecular mechanisms of endocrine autonomy in these tumors, we performed... 
UBPY | ENDOSOMES | DOMAIN | PROTEIN | EPIDERMAL-GROWTH-FACTOR | GENETICS & HEREDITY | UBIQUITYLATION | DEGRADATION | RECEPTOR DOWN-REGULATION | ENDOCYTIC TRAFFICKING | PITUITARY-ADENOMAS | Adenoma - genetics | Humans | Neoplasm Proteins - physiology | Gene Expression Regulation, Neoplastic | Cercopithecus aethiops | Endosomal Sorting Complexes Required for Transport - genetics | Molecular Sequence Data | Pituitary Neoplasms - complications | ACTH-Secreting Pituitary Adenoma - complications | Pituitary ACTH Hypersecretion - genetics | ACTH-Secreting Pituitary Adenoma - genetics | Receptor, Epidermal Growth Factor - metabolism | Pituitary Neoplasms - secretion | Neoplasm Proteins - genetics | Pro-Opiomelanocortin - genetics | Amino Acid Sequence | ACTH-Secreting Pituitary Adenoma - metabolism | Pituitary Neoplasms - genetics | Ubiquitin Thiolesterase - physiology | Pituitary Neoplasms - metabolism | Ubiquitin Thiolesterase - genetics | 14-3-3 Proteins - metabolism | Adrenocorticotropic Hormone - secretion | Sequence Homology, Amino Acid | Exome - genetics | Sequence Alignment | Animals | Endopeptidases - genetics | ACTH-Secreting Pituitary Adenoma - secretion | Pro-Opiomelanocortin - biosynthesis | Mutation | COS Cells | Endosomal Sorting Complexes Required for Transport - physiology | Endopeptidases - physiology | Gene mutations | Cushing syndrome | Physiological aspects | Genetic aspects | Research | Ubiquitin-proteasome system | Health aspects | Risk factors | Pituitary gland | Kinases | Rodents | Genes | Tumors | Index Medicus
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2. Full Text Tumor-directed therapeutic targets in Cushing disease
by Theodoropoulou, Marily and Reincke, Martin
The Journal of clinical endocrinology and metabolism, 12/2018
The most frequent cause of endogenous hypercortisolism is Cushing disease (CD), a devastating condition associated with severe comorbidities and high... 
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3. Full Text Tumor-Directed Therapeutic Targets in Cushing Disease
by Theodoropoulou, Marily and Reincke, Martin
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 03/2019, Volume 104, Issue 3, pp. 925 - 933
Context: The most frequent cause of endogenous hypercortisolism is Cushing disease (CD), a devastating condition associated with severe comorbidities and high... 
NELSONS-SYNDROME | ACTH-SECRETION | BASE-LINE | RETINOIC ACID | CYCLIN-E | BILATERAL ADRENALECTOMY | ENDOCRINOLOGY & METABOLISM | ADRENOCORTICOTROPIN SECRETION | PPAR-GAMMA | TRANSSPHENOIDAL SURGERY | PITUITARY CARCINOMA
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4. Full Text A general overview on pituitary tumorigenesis
by Theodoropoulou, Marily
Annals of Endocrinology (Annales D'Endocrinologie, English Edition), ISSN 0003-4266, 2012, Volume 73, Issue 2, pp. 71 - 72
Internal Medicine | Endocrinology & Metabolism
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5. A general overview on pituitary tumorigenesis
by Theodoropoulou, Marily
Annales d'endocrinologie, 04/2012, Volume 73, Issue 2, p. 71
Pituitary Gland - metabolism | Adenoma - genetics | Cell Transformation, Neoplastic - genetics | Pituitary Gland - pathology | Pituitary Neoplasms - genetics | Humans | Adenoma - pathology | Adenoma - etiology | Pituitary Neoplasms - etiology | Pituitary Neoplasms - pathology
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6. Full Text Stress-responsive FKBP51 regulates AKT2-AS160 signaling and metabolic function
by Balsevich, Georgia and Häusl, Alexander S and Meyer, Carola W and Karamihalev, Stoyo and Feng, Xixi and Pöhlmann, Max L and Dournes, Carine and Uribe-Marino, Andres and Santarelli, Sara and Labermaier, Christiana and Hafner, Kathrin and Mao, Tianqi and Breitsamer, Michaela and Theodoropoulou, Marily and Namendorf, Christian and Uhr, Manfred and Paez-Pereda, Marcelo and Winter, Gerhard and Hausch, Felix and Chen, Alon and Tschöp, Matthias H and Rein, Theo and Gassen, Nils C and Schmidt, Mathias V
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1725 - 12
The co-chaperone FKBP5 is a stress-responsive protein-regulating stress reactivity, and its genetic variants are associated with T2D related traits and other... 
INSULIN | SKELETAL-MUSCLE | IMMUNOPHILIN FKBP51 | GLUCOCORTICOID-RECEPTOR | PROTEIN | MULTIDISCIPLINARY SCIENCES | GROWTH | GENE-EXPRESSION | DIET-INDUCED OBESITY | MICE LACKING | ADIPOSE-TISSUE | Phosphorylation | Tacrolimus Binding Proteins - deficiency | Glucose Transporter Type 4 - metabolism | Signal Transduction | Mice, Inbred C57BL | Stress, Physiological | Male | Tacrolimus Binding Proteins - metabolism | GTPase-Activating Proteins - metabolism | Muscle Fibers, Skeletal - metabolism | Mice, Knockout | Tacrolimus Binding Proteins - genetics | Biological Transport, Active | Animals | Models, Biological | Diet, High-Fat | Glucose - metabolism | Mice | Proto-Oncogene Proteins c-akt - metabolism | Weight Gain | Glucose transporter | Stresses | Myotubes | Body weight | AKT2 protein | Muscles | Homeostasis | Glucose | Insulin | Skeletal muscle | Stress | High fat diet | Glucose tolerance | Genetic variance | Signaling | Antagonism | Clonal deletion | Rodents | Weight reduction | Deletion | Transporter | Index Medicus
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7. Full Text A general overview on pituitary tumorigenesis
by Theodoropoulou, Marily
Annales d'Endocrinologie, ISSN 0003-4266, 04/2012, Volume 73, Issue 2, pp. 71 - 72
ENDOCRINOLOGY & METABOLISM
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8. Full Text High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas
by Maria A Tichomirowa and Anne Barlier and Adrian F Daly and Marie-Lise Jaffrain-Rea and Cristina Ronchi and Maria Yaneva and Jonathan D Urban and Patrick Petrossians and Atanaska Elenkova and Antoine Tabarin and Rachel Desailloud and Dominique Maiter and Thomas Schürmeyer and Renato Cozzi and Marily Theodoropoulou and Caroline Sievers and Ignacio Bernabeu and Luciana A Naves and Olivier Chabre and Carmen Fajardo Montañana and Vaclav Hana and Georges Halaby and Brigitte Delemer and José Ignacio Labarta Aizpún and Emmanuel Sonnet and Ángel Ferrandez Longás and Marie-Thérèse Hagelstein and Philippe Caron and Günter K Stalla and Vincent Bours and Sabina Zacharieva and Anna Spada and Thierry Brue and Albert Beckers
European Journal of Endocrinology, ISSN 0804-4643, 10/2011, Volume 165, Issue 4, pp. 509 - 515
Background: Aryl hydrocarbon receptor interacting protein (AIP) mutations (AIPmut) cause aggressive pituitary adenomas in young patients, usually in the... 
INTERACTING-PROTEIN GENE | ADOLESCENTS | FAMILIES | ENDOCRINOLOGY & METABOLISM | LARGE COHORT | ADENOMA PREDISPOSITION | CHILDREN | Pituitary Neoplasms - epidemiology | Genetic Testing | Prospective Studies | Pituitary Neoplasms - genetics | Humans | Male | Pituitary Neoplasms - pathology | DNA - genetics | Young Adult | Magnetic Resonance Imaging | Mutation - physiology | Adult | Female | Polymorphism, Single Nucleotide | Intracellular Signaling Peptides and Proteins - genetics | Pediatrics | Prolactin | Pituitary | Point mutation | Adenoma | Aryl hydrocarbon receptors | Probes | Age | Index Medicus | Biochemistry, Molecular Biology | Intracellular Signaling Peptides and Proteins | Pituitary Neoplasms | Life Sciences | DNA | Biomolecules | Mutation
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9. Full Text The USP8 mutational status may predict long‐term remission in patients with Cushing's disease
by Albani, Adriana and Pérez‐Rivas, Luis G and Dimopoulou, Christina and Zopp, Stephanie and Colón‐Bolea, Paula and Roeber, Sigrun and Honegger, Jürgen and Flitsch, Jörg and Rachinger, Walter and Buchfelder, Michael and Stalla, Günter K and Herms, Jochen and Reincke, Martin and Theodoropoulou, Marily
Clinical Endocrinology, ISSN 0300-0664, 10/2018, Volume 89, Issue 4, pp. 454 - 458
ObjectiveAlmost half of the cases of Cushing's disease (CD) tumours carry recurrent activating somatic mutations in the ubiquitin-specific protease eight gene... 
pituitary | recurrence | corticotroph tumour | USP | Cushing's disease | remission | adrenocorticotropic hormone | USP8 | MORTALITY | ENDOCRINOLOGY & METABOLISM | ADENOMAS | Ubiquitin | Medical research | Relapse | Proteases | Medicine, Experimental | ACTH | Genetic aspects | Tumors | Diseases | Nervous system diseases | Adrenocorticotropic hormone | Pituitary | Surgery | Remission | Mutation | Hydrocortisone
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10. Full Text Expression of aryl hydrocarbon receptor (AHR) and AHR-interacting protein in pituitary adenomas: pathological and clinical implications
by Marie-Lise Jaffrain-Rea and Mariolina Angelini and Donatella Gargano and Maria A Tichomirowa and Adrian F Daly and Jean-François Vanbellinghen and Emanuela D'Innocenzo and Anne Barlier and Felice Giangaspero and Vincenzo Esposito and Luca Ventura and Antonietta Arcella and Marily Theodoropoulou and Luciana A Naves and Carmen Fajardo and Sabina Zacharieva and Vincent Rohmer and Thierry Brue and Alberto Gulino and Giampaolo Cantore and Edoardo Alesse and Albert Beckers
Endocrine-Related Cancer, ISSN 1351-0088, 09/2009, Volume 16, Issue 3, pp. 1029 - 1043
Germline mutations of the aryl hydrocarbon receptor (AHR)-interacting protein ( AIP ) gene confer a predisposition to pituitary adenomas (PA), usually in the... 
GENE-MUTATIONS | DIOXIN | HORMONE | XAP2 | MESSENGER-RNA | ONCOLOGY | PREDISPOSITION | AIP GENE | ENDOCRINOLOGY & METABOLISM | TCDD | IDENTIFICATION | SECRETING ADENOMAS | Pituitary Gland - metabolism | Adenoma - genetics | Neoplasm Invasiveness | Pituitary Neoplasms - genetics | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Receptors, Aryl Hydrocarbon - genetics | Pituitary Neoplasms - pathology | Intracellular Signaling Peptides and Proteins - metabolism | Pituitary Neoplasms - metabolism | Adenoma - metabolism | Prolactinoma - genetics | Prolactinoma - metabolism | Young Adult | Phenotype | Adolescent | Adenoma - pathology | Receptors, Aryl Hydrocarbon - metabolism | Adult | Mutation | Child | Intracellular Signaling Peptides and Proteins - genetics | Prolactinoma - pathology | Index Medicus
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11. Full Text c-Src regulates Akt signaling in response to ghrelin via β-arrestin signaling-independent and -dependent mechanisms
by Lodeiro, Maria and Theodoropoulou, Marily and Pardo, Maria and Casanueva, Felipe F and Casamiña, Jesus P
PLoS ONE, ISSN 1932-6203, 03/2009, Volume 4, Issue 3, pp. e4686 - e4686
The aim of the present study was to identify the signaling mechanisms to ghrelin-stimulated activation of the serine/threonine kinase Akt. In human embryonic... 
BIOLOGY | Cell Line | Phosphorylation | Signal Transduction | src-Family Kinases | Humans | 3T3-L1 Cells | Arrestins - metabolism | Protein Transport | Ghrelin - metabolism | Protein-Tyrosine Kinases - physiology | Animals | beta-Arrestins | Proto-Oncogene Proteins - physiology | Receptors, Ghrelin - metabolism | Mice | Enzyme Activation | Proto-Oncogene Proteins c-akt - metabolism | GTP-Binding Protein alpha Subunits, Gi-Go - metabolism | Laboratories | Colorectal cancer | AKT protein | Activation | Arrestin | Insulin-like growth factors | Metastasis | Kinases | Recruitment | Proteins | Signal transduction | Ghrelin | Rodents | Polyclonal antibodies | Transducers | Threonine | Src protein | 1-Phosphatidylinositol 3-kinase | Scaffolding | Growth hormones | Ligands | Protein-serine/threonine kinase | Regulation | Endocrinology | Apoptosis | Kidney transplantation | Index Medicus
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12. Full Text Transcriptome analysis of MENX-associated rat pituitary adenomas identifies novel molecular mechanisms involved in the pathogenesis of human pituitary gonadotroph adenomas
by Lee, Misu and Marinoni, Ilaria and Irmler, Martin and Psaras, Tsambika and Honegger, Jürgen B and Beschorner, Rudi and Anastasov, Natasa and Beckers, Johannes and Theodoropoulou, Marily and Roncaroli, Federico and Pellegata, Natalia S
Acta Neuropathologica, ISSN 0001-6322, 7/2013, Volume 126, Issue 1, pp. 137 - 150
Gonadotroph adenomas comprise 15–40 % of all pituitary tumors, are usually non-functioning and are often large and invasive at presentation. Surgery is the... 
Pathology | Neurosciences | Transcriptome analysis | MENX model | Medicine & Public Health | CYP11A1 | NUSAP1 | Pituitary gonadotroph adenoma | RECEPTOR | PATTERNS | PROLIFERATION | PATHOLOGY | DIFFERENTIAL GENE-EXPRESSION | TUMORS | CANCER | NEUROSCIENCES | CLINICAL NEUROLOGY | INVASION | CHECKPOINT | DOSAGE | Cholesterol Side-Chain Cleavage Enzyme - metabolism | Microtubule-Associated Proteins - genetics | Adenoma - genetics | Microtubule-Associated Proteins - metabolism | Humans | Gene Expression Profiling | Green Fluorescent Proteins - genetics | Cholesterol Side-Chain Cleavage Enzyme - genetics | Transfection | Cell Transformation, Neoplastic - genetics | Microarray Analysis | RNA Interference - physiology | Gene Expression Regulation, Neoplastic - genetics | Biostatistics | Green Fluorescent Proteins - metabolism | Pituitary Neoplasms - genetics | Gonadotropins, Pituitary - metabolism | Computational Biology | Rats | Pituitary Neoplasms - pathology | Transcription Factors - genetics | Transcription Factors - metabolism | Animals | Adenoma - pathology | Cell Line, Tumor | Immunohistochemistry | Physiological aspects | Criminal investigation | Cytochrome P-450 | Tumors | Index Medicus | Original Paper
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13. Full Text Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson’s tumor
by Pérez-Rivas, Luis G and Theodoropoulou, Marily and Puar, Troy H and Fazel, Julia and Stieg, Mareike R and Ferraù, Francesco and Assié, Guillaume and Gadelha, Monica R and Deutschbein, Timo and Fragoso, Maria C and Kusters, Benno and Saeger, Wolfgang and Honegger, Jürgen and Buchfelder, Michael and Korbonits, Márta and Bertherat, Jérôme and Stalla, Günter K and Hermus, Ad R and Beuschlein, Felix and Reincke, Martin
European Journal of Endocrinology, ISSN 0804-4643, 01/2018, Volume 178, Issue 1, pp. 57 - 63
Objective Somatic mutations in the ubiquitin-specific protease 8 (USP8) gene are frequent in corticotroph tumors causing Cushing’s disease (CD). Corticotroph... 
Ubiquitin | Nervous system diseases | Ubiquitin-specific proteinase | Visual field | Adenoma | Adrenalectomy | Body mass index | Adrenocorticotropic hormone | Pituitary | Surgery | Mutation | Hyperpigmentation | Tumors
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14. Full Text Loss of function of the tumor suppressor DKC1 perturbs p27 translation control and contributes to pituitary tumorigenesis
by Bellodi, Cristian and Krasnykh, Olya and Haynes, Nikesha and Theodoropoulou, Marily and Peng, Guang and Montanaro, Lorenzo and Ruggero, Davide
Cancer Research, ISSN 0008-5472, 07/2010, Volume 70, Issue 14, pp. 6026 - 6035
Mutations in DKC1, encoding for dyskerin, a pseudouridine synthase that modifies rRNA and regulates telomerase activity, are associated with ribosomal... 
TELOMERASE RNA | SNORNA U50 | GENE | ONCOLOGY | MICE DEFICIENT | CDK INHIBITOR P27 | DYSKERATOSIS-CONGENITA | PROSTATE-CANCER | CELL-CYCLE | HUMAN BREAST-CANCER | RIBOSOMAL-RNA | Translocation, Genetic | Pituitary Neoplasms - genetics | Humans | Middle Aged | Mice, Transgenic | Pituitary Neoplasms - pathology | Pituitary Neoplasms - metabolism | Cell Transformation, Neoplastic - metabolism | Animals | Cyclin-Dependent Kinase Inhibitor p27 - biosynthesis | Cell Transformation, Neoplastic - genetics | Cell Cycle Proteins - genetics | Female | Mice | Mutation | Cell Transformation, Neoplastic - pathology | Nuclear Proteins - genetics | Genes, Tumor Suppressor | Cyclin-Dependent Kinase Inhibitor p27 - genetics | Index Medicus
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15. Full Text Mammalian target of rapamycin inhibitors rapamycin and RAD001 (everolimus) induce anti-proliferative effects in GH-secreting pituitary tumor cells in vitro
by Alexander Gorshtein and Hadara Rubinfeld and Efrat Kendler and Marily Theodoropoulou and Vesna Cerovac and Günter K Stalla and Zvi R Cohen and Moshe Hadani and Ilan Shimon
Endocrine-Related Cancer, ISSN 1351-0088, 09/2009, Volume 16, Issue 3, pp. 1017 - 1027
The effect of mammalian target of rapamycin (mTOR) inhibitors on pituitary tumors is unknown. Akt overexpression was demonstrated in pituitary adenomas, which... 
CYCLOSPORINE-A | PROTEIN | ONCOLOGY | PATHWAY | KINASE | GROWTH | ENDOCRINOLOGY & METABOLISM | CYCLE ARREST | EXPRESSION | HUMAN CANCER | P27(KIP1) | MTOR | Protein Kinases - metabolism | Adenoma - genetics | Humans | Growth Hormone-Secreting Pituitary Adenoma - genetics | E2F Transcription Factors - metabolism | Adenoma - metabolism | Growth Hormone-Secreting Pituitary Adenoma - metabolism | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | Phosphorylation - drug effects | Tumor Cells, Cultured | Drug Evaluation, Preclinical | Everolimus | Cyclin D3 - metabolism | Cell Survival - drug effects | Sirolimus - analogs & derivatives | E2F Transcription Factors - physiology | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Sirolimus - pharmacology | Adenoma - pathology | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | TOR Serine-Threonine Kinases | Cell Cycle - drug effects | Growth Hormone-Secreting Pituitary Adenoma - pathology | Index Medicus
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16. Full Text Silent gonadotroph pituitary neuroendocrine tumor in a patient with tuberous sclerosis complex: evaluation of a possible molecular link
by Regazzo, Daniela and Gardiman, Marina Paola and Theodoropoulou, Marily and Scaroni, Carla and Occhi, Gianluca and Ceccato, Filippo
Endocrinology, diabetes & metabolism case reports, ISSN 2052-0573, 2018, Volume 2018, Issue 1, pp. 1 - 4
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem hereditary cutaneous condition, characterized by multiple hamartomas. In rare cases,... 
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17. Full Text FKBPs and the Akt/mTOR pathway
by Hausch, Felix and Kozany, Christian and Theodoropoulou, Marily and Fabian, Anne-Katrin
Cell Cycle, ISSN 1538-4101, 08/2013, Volume 12, Issue 15, pp. 2366 - 2370
FK506-binding proteins (FKBP) belong to the immunophilin family and are best known for their ability to enable the immunosuppressive properties of FK506 and... 
mTOR | FK506 binding protein | FKBP | Akt | PKB | rapamycin | Rapamycin | MTOR | MAMMALIAN TARGET | ACTIVATION | FK506-BINDING PROTEINS 51 | COMPLEXES | FK506 BINDING-PROTEINS | CELL BIOLOGY | RAPAMYCIN MTOR | INHIBITION | LIGANDS | RHEB | RECEPTORS | TOR Serine-Threonine Kinases - antagonists & inhibitors | Animals | Signal Transduction | TOR Serine-Threonine Kinases - metabolism | Humans | Tacrolimus Binding Proteins - physiology | Proto-Oncogene Proteins c-akt - metabolism | Sirolimus - pharmacology | Index Medicus
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18. Full Text The Gene of the Ubiquitin-Specific Protease 8 Is Frequently Mutated in Adenomas Causing Cushing's Disease
by Perez-Rivas, Luis G and Theodoropoulou, Marily and Ferraù, Francesco and Nusser, Clara and Kawaguchi, Kohei and Stratakis, Constantine A and Faucz, Fabio Rueda and Wildemberg, Luiz E and Assié, Guillaume and Beschorner, Rudi and Dimopoulou, Christina and Buchfelder, Michael and Popovic, Vera and Berr, Christina M and Tóth, Miklós and Ardisasmita, Arif Ibrahim and Honegger, Jürgen and Bertherat, Jerôme and Gadelha, Monica R and Beuschlein, Felix and Stalla, Günter and Komada, Masayuki and Korbonits, Márta and Reincke, Martin
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 07/2015, Volume 100, Issue 7, pp. E997 - E1004
Context: We have recently reported somatic mutations in the ubiquitin-specific protease USP8 gene in a small series of adenomas of patients with Cushing's... 
HUMAN PITUITARY-TUMORS | GROWTH-FACTOR RECEPTOR | RECURRENCE RATES | CORTICOTROPIN-SECRETING TUMORS | ENDOCRINOLOGY & METABOLISM | LONG-TERM REMISSION | TRANSSPHENOIDAL SURGERY | ALPHA | SINGLE-CENTER | MUTATIONS | EXPRESSION | Adenoma - epidemiology | Adenoma - genetics | Humans | Middle Aged | Cercopithecus aethiops | Endosomal Sorting Complexes Required for Transport - genetics | Male | Pituitary ACTH Hypersecretion - genetics | Young Adult | ACTH-Secreting Pituitary Adenoma - genetics | DNA Mutational Analysis | Adult | Female | Retrospective Studies | Tumor Cells, Cultured | Child | Genetic Association Studies | Gene Frequency | Ubiquitin Thiolesterase - genetics | ACTH-Secreting Pituitary Adenoma - epidemiology | Animals | Endopeptidases - genetics | Adolescent | Mice | HeLa Cells | Mutation | COS Cells | Pituitary ACTH Hypersecretion - epidemiology | Index Medicus | Abridged Index Medicus | Advances in Genetics | JCEM Online
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