Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Kutsche

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

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 20 results.
Cytogenetics and Cell Genetics|February 15, 2001
Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epitheliumK Kutsche, E Glauner, S Knauf, et al.
Molecular Pain|September 18, 2012
Sea-anemone toxin ATX-II elicits A-fiber-dependent pain and enhances resurgent and persistent sodium currents in large sensory neuronsAlexandra B Klinger, Mirjam Eberhardt, Andrea S Link, et al.
Cell Systems|October 8, 2018
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human NeurogenesisLisa K Kutsche, Deisy M Gysi, Joerg Fallmann, et al.
Clinical Genetics|September 3, 2013
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutationS Sheikhzadeh, C Sondermann, M Rybczynski, et al.
Clinical Genetics|December 19, 2013
Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutationS Sheikhzadeh, L Brockstaedt, C R Habermann, et al.
Nature Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Clinical Genetics|October 29, 2008
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephalyD J Morris-Rosendahl, J Najm, A M A Lachmeijer, et al.
Clinical Genetics|November 29, 2007
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeA L Schulz, B Albrecht, C Arici, et al.
British Journal of Cancer|March 6, 2015
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromesC P Kratz, L Franke, H Peters, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Cytogenetics and Cell Genetics|February 15, 2001
Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epitheliumK Kutsche, E Glauner, S Knauf, et al.
Molecular Pain|September 18, 2012
Sea-anemone toxin ATX-II elicits A-fiber-dependent pain and enhances resurgent and persistent sodium currents in large sensory neuronsAlexandra B Klinger, Mirjam Eberhardt, Andrea S Link, et al.
Cell Systems|October 8, 2018
Combined Experimental and System-Level Analyses Reveal the Complex Regulatory Network of miR-124 during Human NeurogenesisLisa K Kutsche, Deisy M Gysi, Joerg Fallmann, et al.
Clinical Genetics|September 3, 2013
Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutationS Sheikhzadeh, C Sondermann, M Rybczynski, et al.
Clinical Genetics|December 19, 2013
Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutationS Sheikhzadeh, L Brockstaedt, C R Habermann, et al.
Nature Genetics|January 4, 2001
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DH Bolz, B von Brederlow, A Ramírez, et al.
Nature Genetics|October 4, 2000
Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardationK Kutsche, H Yntema, A Brandt, et al.
Clinical Genetics|October 29, 2008
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephalyD J Morris-Rosendahl, J Najm, A M A Lachmeijer, et al.
Clinical Genetics|November 29, 2007
Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndromeA L Schulz, B Albrecht, C Arici, et al.
British Journal of Cancer|March 6, 2015
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromesC P Kratz, L Franke, H Peters, et al.
Pageof 2