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Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa.
Published in:
Human Genetics, 2002, v. 111, n. 4/5, p. 331, doi. 10.1007/s00439-002-0808-1
By:
- Le Saux, Olivier;
- Beck, Konstanze;
- Sachsinger, Christine;
- Treiber, Carina;
- Göring, Harald H.;
- Curry, Katie;
- Johnson, Eric W.;
- Bercovitch, Lionel;
- Marais, Anna-Susan;
- Terry, Sharon F.;
- Viljoen, Denis L.;
- Boyd, Charles D.
Publication type:
Article
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
Published in:
European Journal of Human Genetics, 2000, v. 8, n. 11, p. 875, doi. 10.1038/sj.ejhg.5200549
By:
- Matsumoto, Naomichi;
- David, Donna E;
- Johnson, Eric W;
- Konecki, David;
- Burmester, James K;
- Ledbetter, David H;
- Weber, James L
Publication type:
Article
SPECT Imaging of the benzodiazepine receptor: Autoradiographic comparison of receptor density and radioligand distribution.
Published in:
Synapse, 1992, v. 12, n. 2, p. 119, doi. 10.1002/syn.890120205
By:
- Sybirska, Elzbieta;
- Al-Tikriti, Mohammed;
- Zoghbi, Sami S.;
- Baldwin, Ronald M.;
- Johnson, Eric W.;
- Innis, Robert B.
Publication type:
Article
Epidermis generated in vitro: practical considerations and applications.
Published in:
Journal of Cellular Biochemistry, 1991, v. 45, n. 3, p. 245, doi. 10.1002/jcb.240450304
By:
- Parenteau, Nancy L.;
- Nolte, Cynthia M.;
- Bilbo, Patrick;
- Rosenberg, Mireille;
- Wilkins, Leon M.;
- Johnson, Eric W.;
- Watson, Stephen;
- Mason, Valerie S.;
- Bell, Eugene
Publication type:
Article
A tunnel section through a prograding Namurian (Arnsbergian, E<sub>2a</sub>) delta, in the western Bowland fells, north Lancashire.
Published in:
Geological Journal, 1981, v. 16, n. 2, p. 93, doi. 10.1002/gj.3350160202
By:
- Johnson, Eric W.
Publication type:
Article
Low frequency of PDCD10 mutations in a panel of CCM3 probands: potential for a fourth CCM locus.
Published in:
Human Mutation, 2006, v. 27, n. 1, p. 118, doi. 10.1002/humu.9389
By:
- Liquori, Christina L.;
- Berg, Michel J.;
- Squitieri, Ferdinando;
- Ottenbacher, Monica;
- Sorlie, Marielle;
- Leedom, Tracey P.;
- Cannella, Milena;
- Maglione, Vittorio;
- Ptacek, Louis;
- Johnson, Eric W.;
- Marchuk, Douglas A.
Publication type:
Article
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1).
Published in:
Human Molecular Genetics, 1999, v. 8, n. 12, p. 2325, doi. 10.1093/hmg/8.12.2325
By:
- Sahoo, Trilochan;
- Johnson, Eric W.;
- Thomas, James W.;
- Kuehl, Peter M.;
- Jones, Thomas L.;
- Dokken, Charles G.;
- Touchman, Jeffrey W.;
- Gallione, Carol J.;
- Lee-Lin, Shih-Queen;
- Kosofsky, Barry;
- Kurth, Janice H.;
- Louis, David N.;
- Mettler, Gabrielle;
- Morrison, Leslie;
- Gil-Nagel, Antonio;
- Rich, Steven S.;
- Zabramski, Joseph M.;
- Boguski, Mark S.;
- Green, Eric D.;
- Marchuk, Douglas A.
Publication type:
Article
Febrile seizures and generalized epilepsy associated with a mutation in the Na<sup>+</sup>-channel ß1 subunit gene SCN1B.
Published in:
Nature Genetics, 1998, v. 19, n. 4, p. 366, doi. 10.1038/1252
By:
- Wallace, Robyn H.;
- Wang, Dao W.;
- Singh, Rita;
- Scheffer, Ingrid E.;
- George, Alfred L.;
- Phillips, Hilary A.;
- Saar, Kathrin;
- Reis, Andre;
- Johnson, Eric W.;
- Sutherland, Grant R.;
- Berkovic, Samuel F.;
- Mulley, John C.
Publication type:
Article
Multilocus Linkage Identifies Two New Loci for a Mendelian Form of Stroke, Cerebral Cavernous Malformation, at 7p15–13 and 3q25.2–27.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 12, p. 1851, doi. 10.1093/hmg/7.12.1851
By:
- Craig, Holly D.;
- Günel, Murat;
- Cepeda, Obed;
- Johnson, Eric W.;
- Ptacek, Louis;
- Steinberg, Gary K.;
- Ogilvy, Christopher S.;
- Berg, Michael J.;
- Crawford, Stephen C.;
- Scott, R. Michael;
- Steichen-Gersdorf, Elizabeth;
- Sabroe, Ruth;
- Kennedy, C. T. C.;
- Mettler, Gabrielle;
- Beis, M. Jill;
- Fryer, Alan;
- Awad, Issam A.;
- Lifton, Richard P.
Publication type:
Article
Multilocus linkage identifies two new loci for a Mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 12, p. 1851, doi. 10.1093/hmg/7.12.1851
By:
- Craig, Holly D.;
- Günel, Murat;
- Cepeda, Obed;
- Johnson, Eric W.;
- Ptacek, Louis;
- Steinberg, Gary K.;
- Ogilvy, Christopher S.;
- Berg, Michael J.;
- Crawford, Stephen C.;
- Scott, R. Michael;
- Steichen‐Gersdorf, Elizabeth;
- Sabroe, Ruth;
- Kennedy, C. T. C.;
- Mettler, Gabrielle;
- Beis, M. Jill;
- Fryer, Alan;
- Awad, Issam A.;
- Lifton, Richard P.
Publication type:
Article
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 1, p. 63, doi. 10.1093/hmg/7.1.63
By:
- Johnson, Eric W.;
- Dubovsky, Jan;
- Rich, Stephen S.;
- O, Cormac A.;
- Orr, Harry T.;
- Anderson, V. Elving;
- Gil‐Nagel, Antonio;
- Ahmann, Peter;
- Dokken, Charles G.;
- Schneider, Derek T.;
- Weber, James L.
Publication type:
Article
Lake District pioneers - the earliest footprints on land.
Published in:
Geology Today, 1996, v. 12, n. 4, p. 147, doi. 10.1046/j.1365-2451.1996.t01-1-00011.x
By:
- Johnson, Eric W.;
- Briggs, Derek E.G.;
- Wright, Joanna L.
Publication type:
Article
SPECT Imaging of the Benzodiazepine Receptor: Feasibility of In Vivo Potency Measurements From Stepwise Displacement Curves.
Published in:
Journal of Nuclear Medicine, 1991, v. 32, n. 9, p. 1754
By:
- Innis, Robert B.;
- Al-Tikriti, Mohammed S.;
- Zoghbi, Sami S.;
- Baldwin, Ronald M.;
- Sybirska, Elzbieta H.;
- Laruelle, Marc A.;
- Malison, Robert T.;
- Seibyl, John P.;
- Zimmermann, Ralf C.;
- Johnson, Eric W.;
- Smith, Eileen O.;
- Charney, Dennis S.;
- Heninger, George R.;
- Woods, Scott W.;
- Hoffer, Paul B.
Publication type:
Article

Found: 13