Kenwrick, S.J.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Somatic and germ line mosaicism and mutation origin for a mutation in theL1 gene in a family with X-linked hydrocephalus

Du, Jian-Sheng, Bason, Lynne, Woffendin, Hayley, Zackai, Elaine, Kenwrick, Susan

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 124 KB

english, 1998

2

Molecular analysis of human muscular dystrophies

Dr. K. E. Davies, S. Forrest, T. Smith, S. Kenwrick, S. Ball, H. Dorkins, M. Patterson

Journal:

Year:

1987

Language:

english

File:

PDF, 719 KB

english, 1987

3

A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti

Julie Steffann, Valérie Raclin, Asmae Smahi, Hayley Woffendin, Arnold Munnich, Sue J. Kenwrick, Anne-Gaelle Grebille, Alexandra Benachi, Yves Dumez, Jean-Paul Bonnefont, Smaïl Hadj-Rabia

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 123 KB

english, 2004

4

The complete sequence of the human locus for NgCAM-related cell adhesion molecule reveals a novel alternative exon in chick and man and conserved genomic organization for the L1 subfamily

Kate Dry, Sue Kenwrick, André Rosenthal, Matthias Platzer

Journal:

Year:

2001

Language:

english

File:

PDF, 266 KB

english, 2001

5

The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish Fugu

Oliver Coutelle, Gerald Nyakatura, Stefan Taudien, Greg Elgar, Sydney Brenner, Matthias Platzer, Bernd Drescher, Monique Jouet, Sue Kenwrick, André Rosenthal

Journal:

Year:

1998

Language:

english

File:

PDF, 306 KB

english, 1998

6

[IEEE 2016 Australasian Universities Power Engineering Conference (AUPEC) - Brisbane, Australia (2016.9.25-2016.9.28)] 2016 Australasian Universities Power Engineering Conference (AUPEC) - Validation and calibration of the blackwall SVC AVR and POD models

Memisevic, Rizah, Kamberovic, Aljosa, Kenwrick, Anthony

Year:

2016

Language:

english

File:

PDF, 702 KB

english, 2016

7

Human homologue of the murinebare patches/striated gene is not mutated in incontinentia pigmenti type 2

Aradhya, Swaroop, Nelson, David L., Heiss, Nina S., Poustka, Annemarie, Woffendin, Hayley, Kenwrick, Susan, Esposito, Teresa, Ciccodicola, Alfredo, Bardaro, Tiziana, D'Urso, Michele, Smahi, Asmae, Mun

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 477 KB

english, 2000

8

Neural cell adhesion molecule L1: relating disease to function

Sue Kenwrick, Patrick Doherty

Journal:

Year:

1998

Language:

english

File:

PDF, 128 KB

english, 1998

9

Filamin (FLN1), plexin (SEX), major palmitoylated protein p55 (MPP1), and von-Hippel Lindau binding protein (VBP1) are not involved in incontinentia pigmenti type 2

Swaroop Aradhya, Pallavi Ahobila, Richard Alan Lewis, David L. Nelson, Teresa Esposito, Alfredo Ciccodicola, Tiziana Bardaro, Michele D'Urso, Hayley Woffendin, Susan Kenwrick, Asmae Smahi, Solange Heu

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 406 KB

english, 2000

10

Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection

S. Mansour, H. Woffendin, S. Mitton, I. Jeffery, T. Jakins, S. Kenwrick, V.A. Murday

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 222 KB

english, 2001

11

Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome

Dr. K. E. Davies, M. N. Patterson, S. J. Kenwrick, M. V. Bell, H. R. Sloan, J. A. Westman, L. J. Elsas II, J. Mahan, John M. Optiz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1988

Language:

english

File:

PDF, 457 KB

english, 1988

12

Pilot morpholino screen in Xenopus tropicalis identifies a novel gene involved in head development

Sue Kenwrick, Enrique Amaya, Nancy Papalopulu

Journal:

Developmental Dynamics

Year:

2004

Language:

english

File:

PDF, 2.37 MB

english, 2004

13

Tumour cells in metastatic deposits with altered sensitivity to natural killer cells

Colin G. Brooks, Graham R. Flannery, Neville Willmott, Eric B. Austin, Susan Kenwrick, Robert W. Baldwin

Journal:

International Journal of Cancer

Year:

1981

Language:

english

File:

PDF, 718 KB

english, 1981

14

X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisation

Hayley Woffendin, Tracy Jakins, Monique Jouet, Helen Stewart, Sarah Landy, Eric Haan, Ann Harris, Dian Donnai, Andrew Read, Sue Kenwrick

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 549 KB

english, 1999

15

Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X Chromosome: implications for mapping human disorders in Xq28

Tiffany A. Angel, Cynthia J. Faust, Juanita C. Gonzales, Susan Kenwrick, Richard Alan Lewis, Gail E. Herman

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 693 KB

english, 1993

16

Linkage studies of X-linked recessive spastic paraplegia using DNA probes

S. Kenwrick, V. Ionasescu, G. Ionasescu, Ch. Searby, A. King, M. Dubowitz, K. E. Davies

Journal:

Year:

1986

Language:

english

File:

PDF, 262 KB

english, 1986

17

Patterns of exon deletions in Duchenne and Becker muscular dystrophy

A. P. Read, R. C. Mountford, S. M. Forrest, S. J. Kenwrick, K. E. Davies, R. Harris

Journal:

Year:

1988

Language:

english

File:

PDF, 475 KB

english, 1988

18

Molecular analysis of muscular dystrophy

Kay E. Davies, Susan J. Kenwrick, Mark N. Patterson, Terry J. Smith, Susan M. Forrest, Huw R. Dorkins, Gareth S. Cross, Sarah B. England

Journal:

Journal of Muscle Research and Cell Motility

Year:

1988

Language:

english

File:

PDF, 885 KB

english, 1988

19

10.1038/35013114

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 403 KB

english, 2000

20

10.1038/35013127

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 180 KB

english, 2000

21

10.1038/35013122

Kenwrick, S. J., The International Incontinentia Pigmenti (IP) Consortium,, France,, Smahi, Asmae, Courtois, G., Vabres, P., Yamaoka, S., Heuertz, S., Munnich, A., Israël, A., Germany,, Heiss, Nina

Journal:

Year:

2000

Language:

english

File:

PDF, 239 KB

english, 2000

22

10.1038/85837

Döffinger, Rainer, Smahi, Asma, Bessia, Christine, Geissmann, Frédéric, Feinberg, Jacqueline, Durandy, Anne, Bodemer, Christine, Kenwrick, Sue, Dupuis-Girod, Sophie, Blanche, Stéphane, Wood, Philip, R

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 600 KB

english, 2001

23

X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 gene

Jouet, Monique, Rosenthal, André, Armstrong, Giles, MacFarlane, John, Stevenson, Roger, Paterson, Joan, Metzenberg, Aïda, Ionasescu, Victor, Temple, Karen, Kenwrick, Susan

Journal:

Nature Genetics

Year:

1994

File:

PDF, 658 KB

1994

24

A missense mutation confirms the L1 defect in X–linked hydrocephalus (HSAS)

Jouet, Monique, Rosenthal, André, MacFarlane, John, Kenwrick, Sue, Donnai, Dian

Journal:

Nature Genetics

Year:

1993

File:

PDF, 117 KB

1993

25

Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X–linked hydrocephalus

Rosenthal, André, Jouet, Monique, Kenwrick, Susan

Journal:

Nature Genetics

Year:

1992

File:

PDF, 717 KB

1992

26

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans

Robertson, Stephen P., Twigg, Stephen R.F., Sutherland-Smith, Andrew J., Biancalana, Valérie, Gorlin, Robert J., Horn, Denise, Kenwrick, Susan J., Kim, Chong A., Morava, Eva, Newbury-Ecob, Ruth

Journal:

Nature Genetics

Year:

2003

Language:

english

File:

PDF, 663 KB

english, 2003

27

Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmenti

Woffendin, Hayley, Esposito, Teresa, Jakins, Tracy, Bardaro, Tiziana, Stern, Marc-Henri, Kenwrick, Sue

Journal:

European Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 55 KB

english, 2000

28

A DNA Fragment from Xq21 Replaces a Deleted Region Containing the Entire FVIII Gene in a Severe Hemophilia A Patient

Stefania Murru, Letizla Casula, Lucia Casarino, Paolo Moi, Mariano Rocchi, Angela Loi, Annalena Figus, Manuela Mannella, Daniela Poddie, Susan Kenwrick, Piergiorgio Mori, Antonio Cao, Mario Pirastu

Journal:

Year:

1994

File:

PDF, 795 KB

1994

29

Radiation Hybrid Mapping of the Genes for Tenascin-R (TNR), Phosducin (PDC), Laminin C1 (LAMC1), and TAX in 1q25–q32

Hawys Williams, Melitta Schachner, Bo Wang, Susan Kenwrick

Journal:

Year:

1997

Language:

english

File:

PDF, 72 KB

english, 1997

30

Physical and Genetic Characterization Reveals a Pseudogene, an Evolutionary Junction, and Unstable Loci in Distal Xq28

Swaroop Aradhya, Hayley Woffendin, Penelope Bonnen, Nina S. Heiss, Takanori Yamagata, Teresa Esposito, Tiziana Bardaro, Annemarie Poustka, Michele D'Urso, Sue Kenwrick, David L. Nelson

Journal:

Year:

2002

Language:

english

File:

PDF, 423 KB

english, 2002

31

Neural cell recognition molecule L1: from cell biology to human hereditary brain malformations

Thomas Brümmendorf, Susan Kenwrick, Fritz G Rathjen

Journal:

Current Opinion in Neurobiology

Year:

1998

Language:

english

File:

PDF, 1.03 MB

english, 1998

32

Gene analysis of L1 neural cell adhesion molecule in prenatal diagnosis of hydrocephalus

M. Jouet, S. Kenwrick

Journal:

Year:

1995

Language:

english

File:

PDF, 473 KB

english, 1995

33

Evidence for a third transcript from the human factor VIII gene

Levinson, Barbara, Kenwrick, Susan, Gamel, Pamela, Fisher, Karen, Gitschier, Jane

Journal:

Year:

1992

Language:

english

File:

PDF, 968 KB

english, 1992

34

Physical mapping distal to the DMD locus

Love, D.R., Bloomfield, J.F., Kenwrick, S.J., Yates, J.R.W., Davies, K.E.

Journal:

Year:

1990

Language:

english

File:

PDF, 2.26 MB

english, 1990

35

Sequence of the human factor VIII-associated gene is conserved in mouse

Levinson, Barbara, Bermingham, John R., Metzenberg, Aida, Kenwrick, Susan, Chapman, Verne, Gitschier, Jane

Journal:

Year:

1992

Language:

english

File:

PDF, 667 KB

english, 1992

36

A transcribed gene in an intron of the human factor VIII gene

Levinson, Barbara, Kenwrick, Susan, Lakich, Delia, Hammonds, Glenn, Gitschier, Jane

Journal:

Year:

1990

Language:

english

File:

PDF, 2.63 MB

english, 1990

37

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

Kenwrick, Susan, Patterson, Mark, Speer, Astrid, Fischbeck, Kenneth, Davies, Kay

Journal:

Year:

1987

Language:

english

File:

PDF, 2.48 MB

english, 1987

38

Chromosome-specific alpha satellite DNA from human chromosome 1: Hierarchical structure and genomic organization of a polymorphic domain spanning several hundred kilobase pairs of centromeric DNA

Waye, John S., Durfy, Sharon J., Pinkel, Dan, Kenwrick, Susan, Patterson, Mark, Davies, Kay E., Willard, Huntington F.

Journal:

Year:

1987

Language:

english

File:

PDF, 1.11 MB

english, 1987

39

The Molecular Genetics of Human Monogenic Diseases

Ball, S.P., Kenwrick, S.J., Davies, K.E.

Journal:

Biotechnology and Genetic Engineering Reviews

Year:

1985

Language:

english

File:

PDF, 2.52 MB

english, 1985

40

Alternative Use of a Mini Exon of the L1 Gene Affects L1 Binding to Neural Ligands

De Angelis, E., Brummendorf, T., Cheng, L., Lemmon, V., Kenwrick, S.

Journal:

Journal of Biological Chemistry

Year:

2001

Language:

english

File:

PDF, 617 KB

english, 2001

41

Isolation and sequence of two genes associated with a CpG island 5′ of the factor VIII gene

Kenwrick, Susan, Levinson, Barbara, Taylor, Sherry, Shapiro, Amy, Gitschier, Jane

Journal:

Human Molecular Genetics

Year:

1992

Language:

english

File:

PDF, 5.66 MB

english, 1992

42

X linked hydrocephalus and MASA syndrome.

Kenwrick, S, Jouet, M, Donnai, D

Journal:

Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 1.82 MB

english, 1996

43

Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family

Coucke, Paul, Vits, Lleve, Camp, Guy Van, Serville, Francoise, Lyonnet, Stanislas, Kenwrick, Susan, Rosenthal, André, Wehnert, Manfred, Munnich, Arnold, Willems, Patrick J.

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.81 MB

english, 1994

44

Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Jouet, M, Feldman, E, Yates, J, Donnai, D, Paterson, J, Siggers, D, Kenwrick, S

Journal:

Journal of Medical Genetics

Year:

1993

Language:

english

File:

PDF, 612 KB

english, 1993

45

A Taql polymorphism adjacent to the factor VIII gene (F8C)

Kenwrick, S., Bridge, P., Lillicrap, D., Lehesjoki, A.-E., Bainton, J., Gitschier, J.

Journal:

Nucleic Acids Research

Year:

1991

Language:

english

File:

PDF, 1.77 MB

english, 1991

46

Discordant segregation of Xq28 markers and a mutation in the L1 gene in a family with X linked hydrocephalus.

Jouet, M, Strain, L, Bonthron, D, Kenwrick, S

Journal:

Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 640 KB

english, 1996

47

Localization of the human TAX-1 gene to 1q32.1: a region implicated in microcephaly and Van der Woude syndrome

Kenwrick, Susan, Leversha, Margaret, Rooke, Lesley, Hasler, Thomas, Sonderegger, Peter

Journal:

Human Molecular Genetics

Year:

1993

Language:

english

File:

PDF, 2.08 MB

english, 1993

48

Localisation of the endpoints of deletions in the 5′ region of the Duchenne gene using a sequence isolated by chromosome jumping

Kenwrick, Susan J., Smith, Terry J., England, Sarah, Collins, Francis, Davies, Kay E.

Journal:

Nucleic Acids Research

Year:

1988

Language:

english

File:

PDF, 4.03 MB

english, 1988

49

SPIE Proceedings [SPIE SPIE BiOS - San Francisco, California, USA (Saturday 2 February 2013)] Optical Tomography and Spectroscopy of Tissue X - Development of transrectal diffuse optical tomography combined with 3D-transrectal ultrasound imaging to monitor the photocoagulation front during interstitial photothermal therapy of primary focal prostate cancer

He, Jie, Weersink, Robert, Veilleux, Israel, Mayo, Kenwrick, Zhang, Anqi, Piao, Daqing, Alam, Adeel, Trachtenberg, John, Wilson, Brian C., Tromberg, Bruce J., Yodh, Arjun G., Sevick-Muraca, Eva M.

Year:

2013

Language:

english

File:

PDF, 766 KB

english, 2013

50

[IEEE 2016 Australasian Universities Power Engineering Conference (AUPEC) - Brisbane, Australia (2016.9.25-2016.9.28)] 2016 Australasian Universities Power Engineering Conference (AUPEC) - Power oscillation damper design — Blackwall SVC

Memisevic, Rizah, Kamberovic, Aljosa, Fonseka, Jagath, Gilmour, Sarah, Kenwrick, Anthony

Year:

2016

Language:

english

File:

PDF, 1.40 MB

english, 2016

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@z-lib.do

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски