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1

The imprinted gene Magel2 regulates normal circadian output

Kozlov, Serguei V, Bogenpohl, James W, Howell, Maureen P, Wevrick, Rachel, Panda, Satchin, Hogenesch, John B, Muglia, Louis J, Van Gelder, Russell N, Herzog, Erik D, Stewart, Colin L

Journal:

Nature Genetics

Year:

2007

Language:

english

File:

PDF, 636 KB

english, 2007

2

Class-uniformly resolvable designs with block sizes 2 and 3

D. Wevrick, S. A. Vanstone

Journal:

Journal of Combinatorial Designs

Year:

1996

Language:

english

File:

PDF, 1.24 MB

english, 1996

3

Genetic analysis of very obese children with autism spectrum disorder

Cortes, Herman D., Wevrick, Rachel

Journal:

Molecular Genetics and Genomics

Year:

2018

Language:

english

File:

PDF, 1.47 MB

english, 2018

4

ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison

Barclay, Sarah F., Rand, Casey M., Nguyen, Lisa, Wilson, Richard J. A., Wevrick, Rachel, Gibson, William T., Bech-Hansen, N. Torben, Weese-Mayer, Debra E.

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 616 KB

english, 2018

5

Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene Magel2

Rebecca E. Mercer, Erin M. Kwolek, Jocelyn M. Bischof, Matthijs van Eede, R. Mark Henkelman, Rachel Wevrick

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2009

Language:

english

File:

PDF, 356 KB

english, 2009

6

A MAGE/NDN-like gene in zebrafish

Jocelyn M. Bischof, Marc Ekker, Rachel Wevrick

Journal:

Developmental Dynamics

Year:

2003

Language:

english

File:

PDF, 179 KB

english, 2003

7

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons

Alysa A. Tennese, Christopher B. Gee, Rachel Wevrick

Journal:

Developmental Dynamics

Year:

2008

Language:

english

File:

PDF, 3.32 MB

english, 2008

8

Loss of Necdin impairs myosin activation and delays cell polarization

Jason R. Bush, Rachel Wevrick

Journal:

Year:

2010

Language:

english

File:

PDF, 1.20 MB

english, 2010

9

Chromatin modification of the human imprinted NDN (necdin) gene detected by in vivo footprinting

Meredith L. Hanel, Jason C.Y. Lau, Isabelle Paradis, Régen Drouin, Rachel Wevrick

Journal:

Journal of Cellular Biochemistry

Year:

2005

Language:

english

File:

PDF, 422 KB

english, 2005

10

Singular points in pair covers and their relation to Hadamard designs

R.C. Mullin, Dan Wevrick

Journal:

Discrete Mathematics

Year:

1991

Language:

english

File:

PDF, 351 KB

english, 1991

11

The role of genomic imprinting in human developmental disorders: lessons from Prader–Willi syndrome

Ml Hanel, R Wevrick

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 176 KB

english, 2001

12

Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells

Julia Devos, Sara V Weselake, Rachel Wevrick

Journal:

Journal of Circadian Rhythms

Year:

2011

Language:

english

File:

PDF, 519 KB

english, 2011

13

Mapping of the murine and ratFaccgenes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group C

Rachel Wevrick, Jane E. Barker, Joseph H. Nadeau, Claude Szpirer, Manuel Buchwald

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 739 KB

english, 1993

14

Human centromeric DNAs

C. Lee, R. Wevrick, R. B. Fisher, M. A. Ferguson-Smith, C. C. Lin

Journal:

Year:

1997

Language:

english

File:

PDF, 112 KB

english, 1997

15

The Prader–Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation

Jason R. Bush, Rachel Wevrick

Journal:

Differentiation

Year:

2008

Language:

english

File:

PDF, 438 KB

english, 2008

16

10.1038/13828

Stewart, Colin L., Gérard, Matthieu, Hernandez, Lidia, Wevrick, Rachel

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 1.11 MB

english, 1999

17

A mouse model for Prader-Willi syndrome imprinting-centre mutations

Yang, Tao, Adamson, Todd E., Resnick, James L., Leff, Stuart, Wevrick, Rachel, Francke, Uta, Jenkins, Nancy A., Copeland, Neal G., Brannan, Camilynn I.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 1.11 MB

1998

18

Evaluation of Prader-Willi Syndrome Gene MAGEL2 in Severe Childhood-Onset Obesity

Megan A. O'Neill, I. Sadaf Farooqi, Rachel Wevrick

Journal:

Year:

2005

Language:

english

File:

PDF, 39 KB

english, 2005

19

Energy homeostasis in Prader–Willi Syndrome: How clinical research informs studies of animal models of genetic obesity : Comment on “Nutritional Phases in Prader-Willi Syndrome,” Miller et al., 2011. Am J Med Genet Part A, 155:1040–1049

Rebecca E. Mercer, Rachel Wevrick

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 64 KB

english, 2012

20

'Glow in the Dark' crayons as inexpensive autoradiography markers

Syann Lee, Rachel Wevrick

Journal:

Technical Tips Online

Year:

1997

Language:

english

File:

PDF, 125 KB

english, 1997

21

Prader–Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

Syann Lee, Christine L. Walker, Rachel Wevrick

Journal:

Gene Expression Patterns

Year:

2003

Language:

english

File:

PDF, 757 KB

english, 2003

22

A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues

Thea K Chibuk, Jocelyn M Bischof, Rachel Wevrick

Journal:

Year:

2001

Language:

english

File:

PDF, 798 KB

english, 2001

23

Expression of the Fanconi Anemia Gene FAC in Human Cell Lines: Lack of Effect of Oxygen Tension

Hans Joenje, Hagop Youssoufian, Frank A.E. Kruyt, Claudia C. dos Santos, Rachel Wevrick, Manuel Buchwald

Journal:

Blood Cells, Molecules, and Diseases

Year:

1995

Language:

english

File:

PDF, 2.36 MB

english, 1995

24

Loss of the Prader–Willi obesity syndrome protein necdin promotes adipogenesis

Jason Russell Bush, Rachel Wevrick

Journal:

Year:

2012

Language:

english

File:

PDF, 845 KB

english, 2012

25

Developmental Abnormalities of Neuronal Structure and Function in Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin

Silvia Pagliardini, Jun Ren, Rachel Wevrick, John J. Greer

Journal:

The American Journal of Pathology

Year:

2005

Language:

english

File:

PDF, 3.86 MB

english, 2005

26

Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control

Syann Lee, Rachel Wevrick

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 462 KB

english, 2000

27

Co-morbidity of complex genetic disorders and hypersomnias of central origin: lessons from the underlying neurobiology of wake and sleep

SV Weselake, R Wevrick

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 526 KB

english, 2012

28

Diagnostic test for the Prader-Willi syndrome by SNRPN expression in blood

Rachel Wevrick, Uta Francke

Journal:

Year:

1996

Language:

english

File:

PDF, 222 KB

english, 1996

29

SPEECH THERAPY

Mrs. PATRICIA WEVRICK

Journal:

Australian Occupational Therapy Journal

Year:

1960

Language:

english

File:

PDF, 420 KB

english, 1960

30

Recommendations for the investigation of animal models of Prader–Willi syndrome

James L. Resnick, Robert D. Nicholls, Rachel Wevrick

Journal:

Mammalian Genome

Year:

2013

Language:

english

File:

PDF, 327 KB

english, 2013

31

Mammalian DNA-repair genes

Wevrick, Rachel, Buchwald, Manuel

Journal:

Current Opinion in Genetics & Development

Year:

1993

Language:

english

File:

PDF, 637 KB

english, 1993

32

Loss of the Circadian Rhythm Gene Magel2 Leads to Metabolic Changes and Reduced Fertility in Mice.

Mercer, Rebecca E., Wevrick, Rachel

Journal:

Canadian Journal of Diabetes

Year:

2008

Language:

english

File:

PDF, 739 KB

english, 2008

33

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7

Wevrick, Rachel, Willard, Vicki P., Willard, Huntington F.

Journal:

Year:

1992

Language:

english

File:

PDF, 3.05 MB

english, 1992

34

Loss of the Prader-Willi Syndrome candidate gene Magel2 alters appetite energy balance

Mercer, R.E., Wevrick, R.

Journal:

Canadian Journal of Diabetes

Year:

2009

Language:

english

File:

PDF, 436 KB

english, 2009

35

Long-Range Organization of Tandem Arrays of α Satellite DNA at the Centromeres of Human Chromosomes: High-Frequency Array-Length Polymorphism and Meiotic Stability

Rachel Wevrick and Huntington F. Willard

Journal:

Proceedings of the National Academy of Sciences

Year:

1989

Language:

english

File:

PDF, 1.26 MB

english, 1989

36

Evolution of bubbles in vacuum

Lake, Kayll, Wevrick, Rachel

Journal:

Canadian Journal of Physics

Year:

1986

Language:

english

File:

PDF, 338 KB

english, 1986

37

Evaluation of melanoma antigen (MAGE) gene expression in human cancers using The Cancer Genome Atlas

Li, Xiao, Hughes, Sarah C., Wevrick, Rachel

Journal:

Cancer Genetics

Year:

2015

Language:

english

File:

PDF, 923 KB

english, 2015

38

Leptin signaling defects in a mouse model of Prader-Willi syndrome

Colmers, William F., Wevrick, Rachel

Journal:

Year:

2013

Language:

english

File:

PDF, 309 KB

english, 2013

39

Response Set in a Multiple-Choice Test

Journal:

Educational and Psychological Measurement

Year:

1962

Language:

english

File:

PDF, 256 KB

english, 1962

40

Establishment and Maintenance of DNA Methylation Patterns in Mouse Ndn: Implications for Maintenance of Imprinting in Target Genes of the Imprinting Center

Hanel, M. L., Wevrick, R.

Journal:

Molecular and Cellular Biology

Year:

2001

Language:

english

File:

PDF, 169 KB

english, 2001

41

Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome

Bischof, J. M., Stewart, C. L., Wevrick, R.

Journal:

Human Molecular Genetics

Year:

2007

Language:

english

File:

PDF, 116 KB

english, 2007

42

Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development

Miller, N. L.G., Wevrick, R., Mellon, P. L.

Journal:

Human Molecular Genetics

Year:

2008

Language:

english

File:

PDF, 1006 KB

english, 2008

43

Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the Magel2 -null mouse model of Prader–Willi syndrome

Pravdivyi, Igor, Ballanyi, Klaus, Colmers, William F., Wevrick, Rachel

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 688 KB

english, 2015

44

Physical map of the centromeric region of human chromosome 7: relationship between two distinct alpha satellite arrays

Wevrick, Rachel, Willard, Huntington F.

Journal:

Nucleic Acids Research

Year:

1991

Language:

english

File:

PDF, 3.39 MB

english, 1991

45

Analysis of DEXI/Dexi refines the organization of the mouse 7C and human 15q11→q13 imprinting clusters

Kelly, M., Edgar, A.J., Wevrick, R.

Journal:

Cytogenetic and Genome Research

Year:

2001

Language:

english

File:

PDF, 188 KB

english, 2001

46

The Necdin Gene is Deleted in Prader-Willi Syndrome and is Imprinted in Human and Mouse

MacDonald, H. R., Wevrick, R.

Journal:

Human Molecular Genetics

Year:

1997

Language:

english

File:

PDF, 324 KB

english, 1997

47

Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice

Mercer, Rebecca E., Michaelson, Sheldon D., Chee, Melissa J. S., Atallah, Tanya A., Wevrick, Rachel, Colmers, William F., Yeo, Giles S. H.

Journal:

Year:

2013

Language:

english

File:

PDF, 1.04 MB

english, 2013

48

Claudin-4 forms a paracellular barrier, revealing the interdependence of claudin expression in the loose epithelial cell culture model opossum kidney cells

Borovac, J., Barker, R. S., Rievaj, J., Rasmussen, A., Pan, W., Wevrick, R., Alexander, R. T.

Journal:

AJP Cell Physiology

Year:

2012

Language:

english

File:

PDF, 1.01 MB

english, 2012

49

Cloning and analysis of the murine Fanconi anemia group C cDNA

Wevrick, Rachel, Clarke, Carol A., Buchwald, Manuel

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 3.88 MB

english, 1993

50

Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia in Magel2 -Null Mice

Tennese, Alysa A., Wevrick, Rachel

Journal:

Year:

2011

Language:

english

File:

PDF, 982 KB

english, 2011

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