PMC Links for Books (Select 1493292) - PMC

Juraj Stanik, Daniela Gasperikova, Magdalena Paskova, Lubomir Barak, Jana Javorkova, Emilia Jancova, Miriam Ciljakova, Peter Hlava, Jozef Michalek, Sarah E. Flanagan, Ewan Pearson, Andrew T. Hattersley, Sian Ellard, Iwar Klimes

J Clin Endocrinol Metab. Author manuscript; available in PMC 2021 Oct 19.

Published in final edited form as: J Clin Endocrinol Metab. 2007 Apr 1; 92(4): 1276–82. Published online 2007 Jan 9. doi: 10.1210/jc.2006-2490

PMCID:: PMC7611849

Article PDF–933K

Select item 76118114.

Mutations in K_ATP Channel Genes cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood

Sarah E. Flanagan, Ann-Marie Patch, Deborah J.G. Mackay, Emma L. Edghill, Anna L. Gloyn, David Robinson, Julian P.H. Shield, Karen Temple, Sian Ellard, Professor Andrew T. Hattersley

Diabetes. Author manuscript; available in PMC 2021 Oct 12.

Published in final edited form as: Diabetes. 2007 Jul 1; 56(7): 1930–7. Published online 2007 Apr 19. doi: 10.2337/db07-0043

PMCID:: PMC7611811

Article PDF–746K

Select item 76118045.

Insulin Mutation Screening in 1044 Patients with Diabetes: Mutations in the INS gene are a Common Cause of Neonatal Diabetes but a Rare Cause of Diabetes Diagnosed in Childhood or Adulthood

Emma L. Edghill, Sarah E. Flanagan, Ann-Marie Patch, Chris Boustred, Andrew Parrish, Beverley Shields, Maggie H. Shepherd, Khalid Hussain, Ritika R. Kapoor, Maciej Malecki, Michael J. MacDonald, Julie Støy, Donald F. Steiner, Louis H. Philipson, Graeme I. Bell, Other members of the Neonatal Diabetes International Collaborative Group: , Andrew T. Hattersley, Sian Ellard

Diabetes. Author manuscript; available in PMC 2021 Oct 11.

Published in final edited form as: Diabetes. 2008 Apr 1; 57(4): 1034–42. Published online 2007 Dec 27. doi: 10.2337/db07-1405

PMCID:: PMC7611804

Article PDF–1.1M

Select item 76118036.

Mutations in the ABCC8 gene encoding the SUR1 subunit of the K_ATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period

A.M. Patch, S.E. Flanagan, C. Boustred, A.T. Hattersley, S. Ellard

Diabetes Obes Metab. Author manuscript; available in PMC 2021 Oct 13.

Published in final edited form as: Diabetes Obes Metab. 2007 Nov 1; 9 Suppl 2(Suppl 2): 28–39. doi: 10.1111/j.1463-1326.2007.00772.x

PMCID:: PMC7611803

Article PDF–1.2M

Select item 68509087.

GATA4 mutations are a cause of neonatal and childhood-onset diabetes

Charles Shaw-Smith, Elisa De Franco, Hana Lango Allen, Marta Batlle, Sarah E. Flanagan, Maciej Borowiec, Craig E. Taplin, Janiëlle van Alfen-van der Velden, Jaime Cruz-Rojo, Guiomar Perez de Nanclares, Zosia Miedzybrodzka, Grazyna Deja, Iwona Wlodarska, Wojciech Mlynarski, Jorge Ferrer, Andrew T. Hattersley, Sian Ellard

Diabetes. Author manuscript; available in PMC 2019 Nov 12.

Published in final edited form as: Diabetes. 2014 Aug 1; 63(8): 2888–2894. Published online 2014 Apr 2. doi: 10.2337/db14-0061

PMCID:: PMC6850908

Article PDF–629K

Select item 50011728.

Isolated Pancreatic Aplasia Due to a Hypomorphic PTF1A Mutation

Jayne A.L. Houghton, Galvin H. Swift, Charles Shaw-Smith, Sarah E. Flanagan, Elisa de Franco, Richard Caswell, Khalid Hussain, Sarar Mohamed, Majedah Abdulrasoul, Andrew T. Hattersley, Raymond J. MacDonald, Sian Ellard

Diabetes. 2016 Sep; 65(9): 2810–2815. Published online 2016 Jun 9. doi: 10.2337/db15-1666

PMCID:: PMC5001172

Article PDF–794K

Select item 48696959.

Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes

Tarig Babiker, Natascia Vedovato, Kashyap Patel, Nicholas Thomas, Roisin Finn, Roope Männikkö, Ali J. Chakera, Sarah E. Flanagan, Maggie H. Shepherd, Sian Ellard, Frances M. Ashcroft, Andrew T. Hattersley

Diabetologia. 2016; 59: 1162–1166. Published online 2016 Mar 31. doi: 10.1007/s00125-016-3921-8

PMCID:: PMC4869695

Article PDF–378K

Select item 464152310.

Age at the time of sulfonylurea initiation influences treatment outcomes in KCNJ11-related neonatal diabetes

Brian W. Thurber, David Carmody, Elizabeth C. Tadie, Ashley N. Pastore, Jazzmyne T. Dickens, Kristen E. Wroblewski, Rochelle N. Naylor, Louis H. Philipson, Siri Atma W. Greeley, the United States Neonatal Diabetes Working Group

Diabetologia. Author manuscript; available in PMC 2016 Jul 1.

Published in final edited form as: Diabetologia. 2015 Jul; 58(7): 1430–1435. Published online 2015 Apr 17. doi: 10.1007/s00125-015-3593-9

PMCID:: PMC4641523

Article PDF–160K

Select item 406296211.

GATA6 haploinsufficiency causes pancreatic agenesis in humans

Hana Lango Allen, Sarah E Flanagan, Charles Shaw-Smith, Elisa De Franco, Ildem Akerman, Richard Caswell, International Pancreatic Agenesis Consortium, Jorge Ferrer, Andrew T Hattersley, Sian Ellard

Nat Genet. Author manuscript; available in PMC 2014 Jun 19.

Published in final edited form as: Nat Genet. 2012 Jan; 44(1): 20–22. Published online 2011 Dec 11. doi: 10.1038/ng.1035

PMCID:: PMC4062962

Article PDF–299K

Select item 399417712.

Microcephaly, Epilepsy and Neonatal Diabetes Due to Compound Heterozygous Mutations in IER3IP1: Insights into the Natural History of a Rare Disorder

Stavit A. Shalev, Yardena Tenenbaum-Rakover, Yoseph Horovitz, Veronica P. Paz, Honggang Ye, David Carmody, Heather M. Highland, Eric Boerwinkle, Craig L. Hanis, Donna M. Muzny, Richard A. Gibbs, Graeme I. Bell, Louis H. Philipson, Siri Atma W. Greeley

Pediatr Diabetes. Author manuscript; available in PMC 2015 May 1.

Published in final edited form as: Pediatr Diabetes. 2014 May; 15(3): 252–256. Published online 2013 Oct 21. doi: 10.1111/pedi.12086

PMCID:: PMC3994177

Article PDF–40K

Select item 388725713.

Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man

Sarah E. Flanagan, Elisa De Franco, Hana Lango Allen, Michele Zerah, Majedah M. Abdul-Rasoul, Julie A. Edge, Helen Stewart, Elham Alamiri, Khalid Hussain, Sam Wallis, Liat de Vries, Oscar Rubio-Cabezas, Jayne A.L. Houghton, Emma L. Edghill, Ann-Marie Patch, Sian Ellard, Andrew T. Hattersley

Cell Metab. 2014 Jan 7; 19(1): 146–154. doi: 10.1016/j.cmet.2013.11.021

PMCID:: PMC3887257

Article PDF–622K

Select item 378713014.

The Krüppel-Like Protein Gli-Similar 3 (Glis3) Functions as a Key Regulator of Insulin Transcription

Gary T. ZeRuth, Yukimasa Takeda, Anton M. Jetten

Mol Endocrinol. 2013 Oct; 27(10): 1692–1705. Published online 2013 Aug 8. doi: 10.1210/me.2013-1117

PMCID:: PMC3787130

Article

Select item 358123415.

GATA6 Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

Elisa De Franco, Charles Shaw-Smith, Sarah E. Flanagan, Maggie H. Shepherd, International NDM Consortium, Andrew T. Hattersley, Sian Ellard

Diabetes. 2013 Mar; 62(3): 993–997. Published online 2013 Feb 14. doi: 10.2337/db12-0885

PMCID:: PMC3581234

Article PDF–539K

Select item 346516116.

Glis3 Regulates Neurogenin 3 Expression in Pancreatic β-Cells and Interacts with Its Activator, Hnf6

Yong-Sik Kim, Hong Soon Kang, Yukimasa Takeda, Lisa Hom, Ho-Yeon Song, Jan Jensen, Anton M. Jetten

Mol Cells. 2012 Aug 31; 34(2): 193–200. Published online 2012 Jul 20. doi: 10.1007/s10059-012-0109-z

PMCID:: PMC3465161

Article PDF–748K

Select item 322606517.

Neonatal Diabetes: An Expanding List of Genes Allows for Improved Diagnosis and Treatment

Siri Atma W. Greeley, Rochelle N. Naylor, Louis H. Philipson, Graeme I. Bell

Curr Diab Rep. Author manuscript; available in PMC 2012 Dec 1.

Published in final edited form as: Curr Diab Rep. 2011 Dec; 11(6): 519–532. doi: 10.1007/s11892-011-0234-7

PMCID:: PMC3226065

Article PDF–342K

Select item 315108418.

Disruption of a Novel Krüppel-like Transcription Factor p300-regulated Pathway for Insulin Biosynthesis Revealed by Studies of the c.-331 INS Mutation Found in Neonatal Diabetes Mellitus

Amélie Bonnefond, Gwen Lomberk, Navtej Buttar, Kanetee Busiah, Emmanuel Vaillant, Stéphane Lobbens, Loïc Yengo, Aurélie Dechaume, Brigitte Mignot, Albane Simon, Raphaël Scharfmann, Bernadette Neve, Sinan Tanyolaç, Ugur Hodoglugil, François Pattou, Hélène Cavé, Juan Iovanna, Roland Stein, Michel Polak, Martine Vaxillaire, Philippe Froguel, Raul Urrutia

J Biol Chem. 2011 Aug 12; 286(32): 28414–28424. Published online 2011 May 18. doi: 10.1074/jbc.M110.215822

PMCID:: PMC3151084

Article PDF–2.1M

Select item 313520319.

Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence

Sara E. Pinney, Jennifer Oliver-Krasinski, Linda Ernst, Nkecha Hughes, Puja Patel, Doris A. Stoffers, Pierre Russo, Diva D. De León

J Clin Endocrinol Metab. 2011 Jul; 96(7): 1960–1965. Published online 2011 Apr 13. doi: 10.1210/jc.2011-0029

PMCID:: PMC3135203

Article

Select item 312019420.

Diabetes and Neurodegeneration in Wolfram Syndrome: A multicenter study of phenotype and genotype

Julia Rohayem, Christian Ehlers, Bärbel Wiedemann, Reinhard Holl, Konrad Oexle, Olga Kordonouri, Giuseppina Salzano, Thomas Meissner, Walter Burger, Edith Schober, Angela Huebner, Min Ae Lee-Kirsch, the Wolfram Syndrome Diabetes Writing Group

Diabetes Care. 2011 Jul; 34(7): 1503–1510. Published online 2011 Jun 17. doi: 10.2337/dc10-1937

PMCID:: PMC3120194

Article PDF–285K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Books

Items: 1 to 20 of 35

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity