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Items: 1 to 20 of 24

1.
Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins
Agata Zygmunt-Górska, Małgorzata Wójcik, Aleksandra Gilis-Januszewska, Anna Starmach, Mirosław Bik-Multanowski, Jerzy B. Starzyk
Hormones (Athens) 2024; 23(1): 69–79. Published online 2023 Dec 26. doi: 10.1007/s42000-023-00510-1
Correction in:
Hormones (Athens). 2024; 23(2): 357.
PMCID:
PMC10847174
AbstractArticlePDF–654K
2.
Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery
Fernanda A. Correa, Marilena Nakaguma, João L. O. Madeira, Mirian Y. Nishi, Milena G. Abrão, Alexander A. L. Jorge, Luciani R. Carvalho, Ivo J. P. Arnhold, Berenice B. Mendonça
Arch Endocrinol Metab. 2019 Mar-Apr; 63(2): 167–174. Published online 2019 May 13. doi: 10.20945/2359-3997000000139
PMCID:
PMC10522137
AbstractArticlePDF–174K
3.
Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency
Ahmed M. Almatrafi, Ali M. Hibshi, Sulman Basit
Medicina (Kaunas) 2023 Mar; 59(3): 474. Published online 2023 Feb 27. doi: 10.3390/medicina59030474
PMCID:
PMC10052823
AbstractArticlePDF–1.7M
4.
Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency
Fatma Derya Bulut, Semine Özdemir Dilek, Damla Kotan, Eda Mengen, Fatih Gürbüz, Bilgin Yüksel
J Clin Res Pediatr Endocrinol. 2020 Sep; 12(3): 261–268. Published online 2020 Sep 2. doi: 10.4274/jcrpe.galenos.2020.2019.0191
PMCID:
PMC7499144
AbstractArticlePDF–443K
5.
Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency
K. Ziemnicka, B. Budny, K. Drobnik, D. Baszko-Błaszyk, M. Stajgis, K. Katulska, R. Waśko, E. Wrotkowska, R. Słomski, M. Ruchała
J Appl Genet. 2016; 57: 373–381. Published online 2015 Nov 25. doi: 10.1007/s13353-015-0328-z
PMCID:
PMC4963446
AbstractArticlePDF–806K
6.
Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations
Petra Dusatkova, Roland Pfäffle, Milton R Brown, Natallia Akulevich, Ivo JP Arnhold, Maria A Kalina, Karolina Kot, Ciril Krzisnik, Manuel C Lemos, Jana Malikova, Ruta Navardauskaite, Barbora Obermannova, Zuzana Pribilincova, Agnes Sallai, Gordana Stipancic, Rasa Verkauskiene, Ondrej Cinek, Werner F Blum, John S Parks, Frederic Austerlitz, Jan Lebl
Eur J Hum Genet. 2016 Mar; 24(3): 415–420. Published online 2015 Jun 10. doi: 10.1038/ejhg.2015.126
PMCID:
PMC4755373
AbstractArticlePDF–565K
7.
Isolated Central Hypothyroidism in Young Siblings as a Manifestation of PROP1 Deficiency: Clinical Impact of Whole Exome Sequencing
Ari J. Wassner, Laurie E. Cohen, Eliana Hechter, Andrew Dauber
Horm Res Paediatr. Author manuscript; available in PMC 2014 May 3.
Published in final edited form as: Horm Res Paediatr. 2013; 79(6): 379–386. Published online 2013 May 3. doi: 10.1159/000350013
PMCID:
PMC3788832
AbstractArticlePDF–1.1M
8.
Regulation of Pituitary Stem Cells by Epithelial to Mesenchymal Transition Events and Signaling Pathways
Leonard Y. M. Cheung, Shannon W. Davis, Michelle L. Brinkmeier, Sally A. Camper, María Inés Pérez-Millán
Mol Cell Endocrinol. Author manuscript; available in PMC 2017 Oct 15.
Published in final edited form as: Mol Cell Endocrinol. 2017 Apr 15; 445: 14–26. Published online 2016 Sep 17. doi: 10.1016/j.mce.2016.09.016
PMCID:
PMC5590650
AbstractArticlePDF–1.1M
9.
Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes
Eleonore Bertko, Jürgen Klammt, Petra Dusatkova, Mithat Bahceci, Nazli Gonc, Louise ten Have, Nurgun Kandemir, Georg Mansmann, Barbora Obermannova, Wilma Oostdijk, Heike Pfäffle, Denise Rockstroh-Lippold, Marina Schlicke, Alpaslan Kemal Tuzcu, Roland Pfäffle
J Hum Genet. 2017 Aug; 62(8): 755–762. Published online 2017 Mar 30. doi: 10.1038/jhg.2017.34
PMCID:
PMC5537413
AbstractArticlePDF–1.0M
10.
PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations
Carolina M.G. Cani, Hamilton Matushita, Luciani R. S. Carvalho, Ibere C. Soares, Luciana P. Brito, Madson Q. Almeida, Berenice B. Mendonça
Clinics (Sao Paulo) 2011 Nov; 66(11): 1849–1854. doi: 10.1590/S1807-59322011001100001
PMCID:
PMC3203954
AbstractArticlePDF–768K
11.
Circulating microRNA profiles and the identification of miR-593 and miR-511 which directly target the PROP1 gene in children with combined pituitary hormone deficiency
YANYAN HU, QIAN WANG, ZENGMIN WANG, FENGXUE WANG, XIAOBO GUO, GUIMEI LI
Int J Mol Med. 2015 Feb; 35(2): 358–366. Published online 2014 Nov 28. doi: 10.3892/ijmm.2014.2016
PMCID:
PMC4292716
AbstractArticlePDF–1.3M
12.
CTNNB1 Gene Mutations, Pituitary Transcription Factors, and MicroRNA Expression Involvement in the Pathogenesis of Adamantinomatous Craniopharyngiomas
Marina Lanciotti Campanini, Leandro Machado Colli, Beatriz Maria Carvalho Paixao, Tatiana Pereira Freitas Cabral, Fernando Colbari Amaral, Helio Rubens Machado, Luciano Serafin Neder, Fabiano Saggioro, Ayrton Custodio Moreira, Sonir Roberto Rauber Antonini, Margaret de Castro
Horm Cancer. 2010 Aug; 1(4): 187–196. Published online 2010 Nov 2. doi: 10.1007/s12672-010-0041-7
PMCID:
PMC10358030
AbstractArticlePDF–185K
13.
Corepressors TLE1 and TLE3 Interact with HESX1 and PROP1
Luciani R. Carvalho, Michelle L. Brinkmeier, Frederic Castinetti, Buffy S. Ellsworth, Sally A. Camper
Mol Endocrinol. 2010 Apr; 24(4): 754–765. Published online 2010 Feb 24. doi: 10.1210/me.2008-0359
PMCID:
PMC2852357
AbstractArticle
14.
All Hormone-Producing Cell Types of the Pituitary Intermediate and Anterior Lobes Derive From Prop1-Expressing Progenitors
Shannon W. Davis, Jessica L. Keisler, María I. Pérez-Millán, Vanessa Schade, Sally A. Camper
Endocrinology. 2016 Apr; 157(4): 1385–1396. Published online 2016 Jan 26. doi: 10.1210/en.2015-1862
PMCID:
PMC4816735
AbstractArticle
15.
A proteome-scale map of the SARS-CoV-2–human contactome
Dae-Kyum Kim, Benjamin Weller, Chung-Wen Lin, Dayag Sheykhkarimli, Jennifer J. Knapp, Guillaume Dugied, Andreas Zanzoni, Carles Pons, Marie J. Tofaute, Sibusiso B. Maseko, Kerstin Spirohn, Florent Laval, Luke Lambourne, Nishka Kishore, Ashyad Rayhan, Mayra Sauer, Veronika Young, Hridi Halder, Nora Marín-de la Rosa, Oxana Pogoutse, Alexandra Strobel, Patrick Schwehn, Roujia Li, Simin T. Rothballer, Melina Altmann, Patricia Cassonnet, Atina G. Coté, Lena Elorduy Vergara, Isaiah Hazelwood, Betty B. Liu, Maria Nguyen, Ramakrishnan Pandiarajan, Bushra Dohai, Patricia A. Rodriguez Coloma, Juline Poirson, Paolo Giuliana, Luc Willems, Mikko Taipale, Yves Jacob, Tong Hao, David E. Hill, Christine Brun, Jean-Claude Twizere, Daniel Krappmann, Matthias Heinig, Claudia Falter, Patrick Aloy, Caroline Demeret, Marc Vidal, Michael A. Calderwood, Frederick P. Roth, Pascal Falter-Braun
Nat Biotechnol. 2023; 41(1): 140–149. Published online 2022 Oct 10. doi: 10.1038/s41587-022-01475-z
PMCID:
PMC9849141
AbstractArticlePDF–7.1M
16.
High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men
Laura M. Yerges, Lambertus Klei, Jane A. Cauley, Kathryn Roeder, Candace M. Kammerer, Susan P. Moffett, Kristine E. Ensrud, Cara S. Nestlerode, Lynn M. Marshall, Andrew R. Hoffman, Cora Lewis, Thomas F. Lang, Elizabeth Barrett-Connor, Robert E. Ferrell, Eric S. Orwoll, Joseph M. Zmuda
J Bone Miner Res. 2009 Dec; 24(12): 2039–2049. Published online 2009 May 18. doi: 10.1359/JBMR.090524
PMCID:
PMC2791518
AbstractArticlePDF–759K
17.
Impact of cytosine methylation on DNA binding specificities of human transcription factors
Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale
Science. Author manuscript; available in PMC 2021 Mar 30.
Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239
PMCID:
PMC8009048
AbstractArticlePDF–2.6M
18.
Assessment of community efforts to advance network-based prediction of protein–protein interactions
Xu-Wen Wang, Lorenzo Madeddu, Kerstin Spirohn, Leonardo Martini, Adriano Fazzone, Luca Becchetti, Thomas P. Wytock, István A. Kovács, Olivér M. Balogh, Bettina Benczik, Mátyás Pétervári, Bence Ágg, Péter Ferdinandy, Loan Vulliard, Jörg Menche, Stefania Colonnese, Manuela Petti, Gaetano Scarano, Francesca Cuomo, Tong Hao, Florent Laval, Luc Willems, Jean-Claude Twizere, Marc Vidal, Michael A. Calderwood, Enrico Petrillo, Albert-László Barabási, Edwin K. Silverman, Joseph Loscalzo, Paola Velardi, Yang-Yu Liu
Nat Commun. 2023; 14: 1582. Published online 2023 Mar 22. doi: 10.1038/s41467-023-37079-7
PMCID:
PMC10033937
AbstractArticlePDF–1.5M
19.
Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study
Swneke D. Bailey, Changchun Xie, Ron Do, Alexandre Montpetit, Rafael Diaz, Viswanathan Mohan, Bernard Keavney, Salim Yusuf, Hertzel C. Gerstein, James C. Engert, Sonia Anand, on behalf of the DREAM investigators
Diabetes Care. 2010 Oct; 33(10): 2250–2253. Published online 2010 Jul 13. doi: 10.2337/dc10-0452
PMCID:
PMC2945168
AbstractArticlePDF–153K
20.
Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip
Philippa J. Talmud, Fotios Drenos, Sonia Shah, Tina Shah, Jutta Palmen, Claudio Verzilli, Tom R. Gaunt, Jacky Pallas, Ruth Lovering, Kawah Li, Juan Pablo Casas, Reecha Sofat, Meena Kumari, Santiago Rodriguez, Toby Johnson, Stephen J. Newhouse, Anna Dominiczak, Nilesh J. Samani, Mark Caulfield, Peter Sever, Alice Stanton, Denis C. Shields, on behalf of the ASCOT investigators, Sandosh Padmanabhan, Olle Melander, Claire Hastie, Christian Delles, on behalf of the NORDIL investigators, Shah Ebrahim, Michael G. Marmot, George Davey Smith, Debbie A. Lawlor, Patricia B. Munroe, for the BRIGHT Consortium, Ian N. Day, Mika Kivimaki, John Whittaker, Steve E. Humphries, Aroon D. Hingorani
Am J Hum Genet. 2009 Nov 13; 85(5): 628–642. doi: 10.1016/j.ajhg.2009.10.014
PMCID:
PMC2775832
AbstractArticlePDF–2.8M

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