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Items: 21

1.

IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivity.

Cryns K, Shamir A, Van Acker N, Levi I, Daneels G, Goris I, Bouwknecht JA, Andries L, Kass S, Agam G, Belmaker H, Bersudsky Y, Steckler T, Moechars D.

Neuropsychopharmacology. 2008 Feb;33(3):674-84. Epub 2007 Apr 25.

2.

Transgenic mice overexpressing glycogen synthase kinase 3beta: a putative model of hyperactivity and mania.

Prickaerts J, Moechars D, Cryns K, Lenaerts I, van Craenendonck H, Goris I, Daneels G, Bouwknecht JA, Steckler T.

J Neurosci. 2006 Aug 30;26(35):9022-9.

3.

Lack of lithium-like behavioral and molecular effects in IMPA2 knockout mice.

Cryns K, Shamir A, Shapiro J, Daneels G, Goris I, Van Craenendonck H, Straetemans R, Belmaker RH, Agam G, Moechars D, Steckler T.

Neuropsychopharmacology. 2007 Apr;32(4):881-91. Epub 2006 Jul 12.

4.

GJB2 mutations and degree of hearing loss: a multicenter study.

Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W, Janecke AR, Nekahm-Heis D, Seeman P, Bendova O, Kenna MA, Frangulov A, Rehm HL, Tekin M, Incesulu A, Dahl HH, du Sart D, Jenkins L, Lucas D, Bitner-Glindzicz M, Avraham KB, Brownstein Z, del Castillo I, Moreno F, Blin N, Pfister M, Sziklai I, Toth T, Kelley PM, Cohn ES, Van Maldergem L, Hilbert P, Roux AF, Mondain M, Hoefsloot LH, Cremers CW, Löppönen T, Löppönen H, Parving A, Gronskov K, Schrijver I, Roberson J, Gualandi F, Martini A, Lina-Granade G, Pallares-Ruiz N, Correia C, Fialho G, Cryns K, Hilgert N, Van de Heyning P, Nishimura CJ, Smith RJ, Van Camp G.

Am J Hum Genet. 2005 Dec;77(6):945-57. Epub 2005 Oct 19.

5.

Energy homeostasis and gastric emptying in ghrelin knockout mice.

De Smet B, Depoortere I, Moechars D, Swennen Q, Moreaux B, Cryns K, Tack J, Buyse J, Coulie B, Peeters TL.

J Pharmacol Exp Ther. 2006 Jan;316(1):431-9. Epub 2005 Oct 3.

PMID:
16203827
6.

Phenotypic and biochemical analyses of BACE1- and BACE2-deficient mice.

Dominguez D, Tournoy J, Hartmann D, Huth T, Cryns K, Deforce S, Serneels L, Camacho IE, Marjaux E, Craessaerts K, Roebroek AJ, Schwake M, D'Hooge R, Bach P, Kalinke U, Moechars D, Alzheimer C, Reiss K, Saftig P, De Strooper B.

J Biol Chem. 2005 Sep 2;280(35):30797-806. Epub 2005 Jun 29.

7.

A genotype-phenotype correlation for GJB2 (connexin 26) deafness.

Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, Smith RJ, Van Camp G.

J Med Genet. 2004 Mar;41(3):147-54.

8.

Circling behavior in the Ecl mouse is caused by lateral semicircular canal defects.

Cryns K, van Alphen AM, van Spaendonck MP, van de Heyning PH, Timmermans JP, de Zeeuw CI, van Camp G.

J Comp Neurol. 2004 Jan 19;468(4):587-95.

PMID:
14689488
9.

Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations.

Pennings RJ, Huygen PL, van den Ouweland JM, Cryns K, Dikkeschei LD, Van Camp G, Cremers CW.

Audiol Neurootol. 2004 Jan-Feb;9(1):51-62.

PMID:
14676474
10.

Deafness genes and their diagnostic applications.

Cryns K, Van Camp G.

Audiol Neurootol. 2004 Jan-Feb;9(1):2-22. Review.

PMID:
14676470
11.

[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].

Pennings RJ, Cryns K, Huygen PL, van Camp G, Cremers CW.

Ned Tijdschr Geneeskd. 2003 Nov 1;147(44):2170-2. Review. Dutch.

PMID:
14626834
12.

Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.

Cryns K, Sivakumaran TA, Van den Ouweland JM, Pennings RJ, Cremers CW, Flothmann K, Young TL, Smith RJ, Lesperance MM, Van Camp G.

Hum Mutat. 2003 Oct;22(4):275-87. Review.

PMID:
12955714
13.

Nonsyndromic hearing loss.

Van Laer L, Cryns K, Smith RJ, Van Camp G.

Ear Hear. 2003 Aug;24(4):275-88. Review.

PMID:
12923419
14.

Molecular characterization of WFS1 in patients with Wolfram syndrome.

van ven Ouweland JM, Cryns K, Pennings RJ, Walraven I, Janssen GM, Maassen JA, Veldhuijzen BF, Arntzenius AB, Lindhout D, Cremers CW, Van Camp G, Dikkeschei LD.

J Mol Diagn. 2003 May;5(2):88-95.

15.

Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).

Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW.

Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):421-6.

PMID:
12707188
16.

The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells.

Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJ, Timmermans JP, Van Camp G.

Histochem Cell Biol. 2003 Mar;119(3):247-56. Epub 2003 Feb 19.

PMID:
12649740
17.

Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.

Bom SJ, Van Camp G, Cryns K, Admiraal RJ, Huygen PL, Cremers CW.

Otol Neurotol. 2002 Nov;23(6):876-84.

PMID:
12438850
18.

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations.

Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, Reardon W, Stephens D, Cremers CW, Smith RJ, Van Camp G.

Hum Genet. 2002 May;110(5):389-94. Epub 2002 Apr 9.

PMID:
12073007
19.

Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes.

Cryns K, Van Spaendonck MP, Flothmann K, van Alphen AM, Van De Heyning PH, Timmermans JP, De Zeeuw CI, Van Camp G.

Genome Res. 2002 Apr;12(4):613-7.

20.

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM.

Hum Mol Genet. 2001 Oct 15;10(22):2501-8.

21.

High resolution imaging of the mouse inner ear by microtomography: a new tool in inner ear research.

Van Spaendonck MP, Cryns K, Van De Heyning PH, Scheuermann DW, Van Camp G, Timmermans JP.

Anat Rec. 2000 Jun 1;259(2):229-36.

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