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Kim Cryns

Showing results (11-20 of 16) with videos related to

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Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|April 27, 2007
IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivityKim Cryns, Alon Shamir, Nathalie Van Acker, et al.
Human Mutation|September 5, 2003
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseKim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, et al.
The Journal of Molecular Diagnostics : JMD|April 23, 2003
Molecular characterization of WFS1 in patients with Wolfram syndromeJohannes M W van ven Ouweland, Kim Cryns, Ronald J E Pennings, et al.
The Journal of Biological Chemistry|July 1, 2005
Phenotypic and biochemical analyses of BACE1- and BACE2-deficient miceDiana Dominguez, Jos Tournoy, Dieter Hartmann, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|April 27, 2007
IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivityKim Cryns, Alon Shamir, Nathalie Van Acker, et al.
Human Mutation|September 5, 2003
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseKim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, et al.
The Journal of Molecular Diagnostics : JMD|April 23, 2003
Molecular characterization of WFS1 in patients with Wolfram syndromeJohannes M W van ven Ouweland, Kim Cryns, Ronald J E Pennings, et al.
The Journal of Biological Chemistry|July 1, 2005
Phenotypic and biochemical analyses of BACE1- and BACE2-deficient miceDiana Dominguez, Jos Tournoy, Dieter Hartmann, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
Pageof 2