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Select item 108471741.

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

Abstract Article PDF–654K

Select item 105221372.

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

Abstract Article PDF–174K

Select item 103580303.

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

Abstract Article PDF–185K

Select item 100528234.

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

Abstract Article PDF–1.7M

Select item 100339375.

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

Abstract Article PDF–1.5M

Select item 98491416.

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

Abstract Article PDF–7.1M

Select item 80090487.

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

Abstract Article PDF–2.6M

Select item 74991448.

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

Abstract Article PDF–443K

Select item 71699839.

A reference map of the human binary protein interactome

Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood

Nature. Author manuscript; available in PMC 2020 Oct 8.

Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x

PMCID:: PMC7169983

Abstract Article PDF–5.4M

Select item 559065010.

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

Abstract Article PDF–1.1M

Select item 553741311.

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

Abstract Article PDF–1.0M

Select item 496344612.

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

Abstract Article PDF–806K

Select item 481673513.

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

Abstract Article

Select item 475537314.

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

Abstract Article PDF–565K

Select item 429271615.

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

Abstract Article PDF–1.3M

Select item 378883216.

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

Abstract Article PDF–1.1M

Select item 320395417.

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

Abstract Article PDF–768K

Select item 317805918.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 294516819.

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

Abstract Article PDF–153K

Select item 285235720.

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

Abstract Article

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