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1

Intrauterine growth restriction—genetic causes and consequences

David Monk, Gudrun E. Moore

Journal:

Seminars in Fetal and Neonatal Medicine

Year:

2004

Language:

english

File:

PDF, 121 KB

english, 2004

2

Iterative augmentation of a medical training simulator: Effects of affective metacognitive scaffolding

Wesiak, Gudrun, Steiner, Christina M., Moore, Adam, Dagger, Declan, Power, Gordon, Berthold, Marcel, Albert, Dietrich, Conlan, Owen

Journal:

Computers & Education

Year:

2014

Language:

english

File:

PDF, 2.59 MB

english, 2014

3

Promiscuous expression of myosin in myotonic dystrophy

Dr. Gudrun E. Moore, Allen D. Roses, Margaret A. Pericak-vance, William E. Garrett Jr, Frederick H. Schachat

Journal:

Year:

1986

Language:

english

File:

PDF, 1.36 MB

english, 1986

4

A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R)

Sayeda Abu-Amero, Michael Preece, Emma Wakeling, Gudrun Moore, Phil Stanier

Journal:

Molecular and Cellular Probes

Year:

1997

Language:

english

File:

PDF, 330 KB

english, 1997

5

Trophoblast from anembryonic pregnancy has both a maternal and a paternal contribution to its genome

Henderson, Deborah J., Bennett, Phillip R., Rodeck, Charles H., Gau, Gillian S., Blunt, Susan, Moore, Gudrun E.

Journal:

American Journal of Obstetrics and Gynecology

Year:

1991

Language:

english

File:

PDF, 1.52 MB

english, 1991

6

Lack of mutations in ZIC3 in three families with neural tube defects

Tessa Carrel, Gail E. Herman, Gudrun E. Moore, Philip Stanier

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 68 KB

english, 2001

7

SNPs in the CpG island of NAP1L2: A possible link between DNA methylation and neural tube defects?

Ute Christine Rogner, Patrick Danoy, Fumihiko Matsuda, Gudrun Elizabeth Moore, Philip Stanier, Philip Avner

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 256 KB

english, 2002

8

Human maternal uniparental disomy for chromosome 16 and fetal development

Mrs Janet Vaughan, Zehra Ali, Sarah Bower, Phillip Bennett, Tim Chard, Gudrun Moore

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 592 KB

english, 1994

9

Novel RFLPs and microsatellite repeats increase informativity at four loci mapping to Xq22-q25

Robert Newton, Philip Stanier, Simon Forbes, Gudrun E. Moore

Journal:

Year:

1994

Language:

english

File:

PDF, 457 KB

english, 1994

10

Molecular analysis of the expression of transthyretin in intestine and liver from trisomy 18 fetuses

Siobhan Loughna, Phillip Bennett, Gudrun Moore

Journal:

Year:

1995

Language:

english

File:

PDF, 766 KB

english, 1995

11

Molecular heterogeneity of histochemical fibre types: a comparison of fast fibres

Gudrun E. Moore, Frederick H. Schachat

Journal:

Journal of Muscle Research and Cell Motility

Year:

1985

Language:

english

File:

PDF, 2.64 MB

english, 1985

12

Patterns of troponin T expression in mammalian fast, slow and promiscuous muscle fibres

Gudrun E. Moore, Margaret M. Briggs, Frederick H. Schachat

Journal:

Journal of Muscle Research and Cell Motility

Year:

1987

Language:

english

File:

PDF, 1.66 MB

english, 1987

13

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed

Megan P. Hitchins, Louise Bentley, David Monk, Colin Beechey, Jo Peters, Gavin Kelsey, Fumitoshi Ishino, Michael A. Preece, Philip Stanier, Gudrun E. Moore

Journal:

Mammalian Genome

Year:

2002

Language:

english

File:

PDF, 181 KB

english, 2002

14

Imprinted methylation profiles for proximal mouse Chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis

David Monk, Rachel Smith, Philippe Arnaud, MichaelA. Preece, Philip Stanier, ColinV. Beechey, Jo Peters, Gavin Kelsey, GudrunE. Moore

Journal:

Mammalian Genome

Year:

2003

Language:

english

File:

PDF, 354 KB

english, 2003

15

Evolutionary conservation, developmental expression, and genomic mapping of mammalianTwisted gastrulation

Daniel Graf, Paula M. Timmons, Megan Hitchins, Vasso Episkopou, Gudrun Moore, Takekito Ito, Asao Fujiyama, Amanda G. Fisher, Matthias Merkenschlager

Journal:

Mammalian Genome

Year:

2001

Language:

english

File:

PDF, 2.19 MB

english, 2001

16

Uniparental disomy: clinical indications for testing in growth retardation

Thomas Eggermann, Klaus Zerres, Katja Eggermann, Gudrun Moore, Hartmut A. Wollmann

Journal:

European Journal of Pediatrics

Year:

2002

Language:

english

File:

PDF, 147 KB

english, 2002

17

Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region

Claire Braybrook, Georgina Warry, Gareth Howell, Vanessa Mandryko, Alfred Arnason, Arni Bjornsson, Mark T. Ross, Gudrun E. Moore, Philip Stanier

Journal:

Year:

2001

Language:

english

File:

PDF, 183 KB

english, 2001

18

Integration of parallel-operating quality systems

Christian Bonk-Kassner, J. Ehmann, Gudrun Gallhoff, David S. Moore, Barbara Moos, Bernd Siegemund

Journal:

Accreditation and Quality Assurance

Year:

1997

Language:

english

File:

PDF, 182 KB

english, 1997

19

The growth hormone receptor gene deleted for exon three (GHRd3) polymorphism is associated with birth and placental weight

Raja Padidela, Sinead M. Bryan, Sayeda Abu-Amero, Rebecca E. Hudson-Davies, John C. Achermann, Gudrun E. Moore, Peter C. Hindmarsh

Journal:

Clinical Endocrinology

Year:

2012

Language:

english

File:

PDF, 86 KB

english, 2012

20

Identification of multiple trisomy using DNA polymorphisms

DEBORAH J. HENDERSON, PHILLIP R. BENNETT, GUDRUN E. MOORE

Journal:

BJOG: An International Journal of Obstetrics & Gynaecology

Year:

1992

Language:

english

File:

PDF, 281 KB

english, 1992

21

Determination of twin zygosity by DNA hybridisation to wild type bacteriophage M13

PHILLIP BENNETT, DEBORAH HENDERSON, PHILIP STANIER, JANET VAUGHAN, GUDRUN MOORE

Journal:

BJOG: An International Journal of Obstetrics & Gynaecology

Year:

1992

Language:

english

File:

PDF, 197 KB

english, 1992

22

Changes in amniotic arachidonic acid metabolism associated with increased cyclo-oxygenase gene expression

Phillip R. Bennett, Donna Slater, Mark Sullivan, Murdoch G. Elder, Gudrun E. Moore

Journal:

BJOG: An International Journal of Obstetrics & Gynaecology

Year:

1993

Language:

english

File:

PDF, 573 KB

english, 1993

23

Linkage of an X-chromosome cleft palate gene

Moore, Gudrun E., Ivens, Alasdair, Chambers, Joanna, Farrall, Martin, Williamson, Robert, Page, David C., Bjornsson, Ami, Arnason, Alfred, Jensson, Olafur

Journal:

Year:

1987

File:

PDF, 233 KB

1987

24

IGF2 is parentally imprinted in human preimplantation embryos

Lighten, Antony D., Hardy, Kate, Winston, Robert M.L., Moore, Gudrun E.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 251 KB

1997

25

10.1038/ng730

Braybrook, Claire, Doudney, Kit, Marçano, Ana Carolina B., Arnason, Alfred, Bjornsson, Arni, Patton, Michael A., Goodfellow, Paul J., Moore, Gudrun E., Stanier, Philip

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 434 KB

english, 2001

26

Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues

Wakeling, Emma L, Abu-Amero, Sayeda N, Stanier, Philip, Preece, Michael A, Moore, Gudrun E

Journal:

European Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 175 KB

english, 1998

27

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome

Hitchins, Megan P, Monk, David, Bell, Gillian M, Ali, Zehra, Preece, Michael A, Stanier, Philip, Moore, Gudrun E

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 297 KB

english, 2001

28

Evidence from skewed X inactivation for trisomy mosaicism in Silver-Russell syndrome

Sharp, Andrew, Moore, Gudrun, Eggermann, Thomas

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 122 KB

english, 2001

29

Expression of mRNA for the insulin-like growth factors and their receptors in human preimplantation embryos

Antony D. Lighten, Kate Hardy, Robert M.L. Winston, Gudrun E. Moore

Journal:

Molecular Reproduction and Development

Year:

1997

Language:

english

File:

PDF, 77 KB

english, 1997

30

Expression of the insulin-like growth factors and their receptors in term placentas: A comparison between normal and IUGR births

Sayeda N. Abu-Amero, Zehra Ali, Philip Bennett, Janet I. Vaughan, Gudrun E. Moore

Journal:

Molecular Reproduction and Development

Year:

1998

Language:

english

File:

PDF, 103 KB

english, 1998

31

Investigation of SUMO pathway genes in the etiology of nonsyndromic cleft lip with or without cleft palate

Eloisa Carta, Erwin Pauws, Anna C. Thomas, Konstantinos Mengrelis, Gudrun E. Moore, Melissa Lees, Philip Stanier

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2012

Language:

english

File:

PDF, 724 KB

english, 2012

32

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

Monk, David, Bentley, Louise, Hitchins, Megan, Myler, Rachael, Clayton-Smith, Jill, Ismail, Samira, Price, Sue, Preece, Michael, Stanier, Philip, Moore, Gudrun

Journal:

Year:

2002

Language:

english

File:

PDF, 387 KB

english, 2002

33

Ontogeny and morphology of the bulbus, part of the male reproductive organ inApis mellifera carnica(Hymenoptera, Apidae)

Lien Moors, Gudrun Koeniger, Johan Billen

Journal:

Year:

2012

Language:

english

File:

PDF, 748 KB

english, 2012

34

Maternal Inheritance of a Promoter Variant in the Imprinted PHLDA2 Gene Significantly Increases Birth Weight

Miho Ishida, David Monk, Andrew J. Duncan, Sayeda Abu-Amero, Jiehan Chong, Susan M. Ring, Marcus E. Pembrey, Peter C. Hindmarsh, John C. Whittaker, Philip Stanier, Gudrun E. Moore

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 293 KB

english, 2012

35

Molecular genetic etiology of twin reversed arterial perfusion sequence

Nicholas M. Fisk, Mark Ware, Philip Stanier, Gudrun Moore, Phillip Bennett

Journal:

American Journal of Obstetrics and Gynecology

Year:

1996

Language:

english

File:

PDF, 694 KB

english, 1996

36

The incidence of uniparental disomy associated with intrauterine growth retardation in a cohort of thirty-five severely affected babies

Gudrun E. Moore, Zehra Ali, Rehan U. Khan, Susan Blunt, Phillip R. Bennett, Janet I. Vaughan

Journal:

American Journal of Obstetrics and Gynecology

Year:

1997

Language:

english

File:

PDF, 800 KB

english, 1997

37

Folate and human development

Kit Doudney, Gudrun Moore

Journal:

Early Human Development

Year:

2002

Language:

english

File:

PDF, 39 KB

english, 2002

38

Refined Mapping and YAC Contig Construction of the X-Linked Cleft Palate and Ankyloglossia Locus (CPX) Including the Proximal X–Y Homology Breakpoint within Xq21.3

Simon A. Forbes, Lyndall Brennan, Michael Richardson, Alison Coffey, Charlotte G. Cole, Simon G. Gregory, David R. Bentley, Steven Mumm, Gudrun E. Moore, Philip Stanier

Journal:

Year:

1996

Language:

english

File:

PDF, 124 KB

english, 1996

39

Identification and Characterization of KLHL4, a Novel Human Homologue of the Drosophila Kelch Gene That Maps within the X-Linked Cleft Palate and Ankyloglossia (CPX) Critical Region

Claire Braybrook, Georgina Warry, Gareth Howell, Alfred Arnason, Arni Bjornsson, Gudrun E. Moore, Mark T. Ross, Philip Stanier

Journal:

Year:

2001

Language:

english

File:

PDF, 380 KB

english, 2001

40

Expression of cyclooxygenase types 1 and 2 in human fetal membranes at term

Donna M. Slater, Louise C. Berger, Robert Newton, Gudrun E. Moore, Phillip R. Bennett

Journal:

American Journal of Obstetrics and Gynecology

Year:

1995

Language:

english

File:

PDF, 2.18 MB

english, 1995

41

Expression of CYP2E1 during human fetal development: methylation of the CYP2E1 gene in human fetal and adult liver samples

Susan M. Jones, Alan R. Boobis, Gudrun E. Moore, Philip M. Stanier

Journal:

Biochemical Pharmacology

Year:

1992

Language:

english

File:

PDF, 641 KB

english, 1992

42

Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of chromosome 1 syntenic with human 1q21–q23

Philip Stanier, Jennifer N. Henson, Jane Eddleston, Gudrun E. Moore, Andrew J. Copp

Journal:

Year:

1995

Language:

english

File:

PDF, 826 KB

english, 1995

43

Molecular cloning and characterization of a highly conserved human 67-kDa laminin receptor pseudogene mapping to Xq21.3

Michael P Richardson, Claire Braybrook, Muly Tham, Gudrun E Moore, Philip Stanier

Journal:

Year:

1998

Language:

english

File:

PDF, 281 KB

english, 1998

44

Genomic Imprinting, Uniparental Disomy and Foetal Growth

Michael A Preece, Gudrun E Moore

Journal:

Trends in Endocrinology & Metabolism

Year:

2000

Language:

english

File:

PDF, 192 KB

english, 2000

45

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome

David Monk, Emma L Wakeling, Virginia Proud, Megan Hitchins, Sayeda N. Abu-Amero, Philip Stanier, Michael A. Preece, Gudrun E Moore

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 1.07 MB

english, 2000

46

Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies

Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier, Caroline A. Sewry, Gudrun E. Moore, Francesco Muntoni

Journal:

The American Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 659 KB

english, 2006

47

TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression

Artemisia M. Andreou, Erwin Pauws, Marius C. Jones, Manvendra K. Singh, Markus Bussen, Kit Doudney, Gudrun E. Moore, Andreas Kispert, Jan J. Brosens, Philip Stanier

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 6.08 MB

english, 2007

48

Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination

Peter E. Clayton, Dan Hanson, Lucia Magee, Philip G. Murray, Emma Saunders, Sayeda N. Abu-Amero, Gudrun E. Moore, Graeme C. M. Black

Journal:

Clinical Endocrinology

Year:

2012

Language:

english

File:

PDF, 231 KB

english, 2012

49

The role of imprinted genes in humans

Ishida, Miho, Moore, Gudrun E.

Journal:

Molecular Aspects of Medicine

Year:

2013

Language:

english

File:

PDF, 922 KB

english, 2013

50

The expression of phospholipase A2 and lipocortins (annexins) I, II and V in human fetal membranes and placenta in association with labour

Phillip Bennett, Donna Slater, Louise Berger, Gudrun Moore

Journal:

Year:

1994

Language:

english

File:

PDF, 706 KB

english, 1994