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D Y Nishimura

Showing results (11-20 of 22) with videos related to

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Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Ophthalmic Genetics|January 5, 2000
Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED lociA B Kanis, A A Al-Rajhi, C M Taylor, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.
Genomics|April 1, 1991
The CEPH consortium linkage map of human chromosome 1N C Dracopoli, P O'Connell, T I Elsner, et al.
Human Molecular Genetics|April 18, 2000
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular developmentR S Smith, A Zabaleta, T Kume, et al.
American Journal of Human Genetics|March 1, 1990
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome IqJ C Murray, D Y Nishimura, K H Buetow, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Genome Research|March 7, 2001
Generation of a high-density rat EST mapT E Scheetz, M R Raymond, D Y Nishimura, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Journal of Glaucoma|December 12, 2001
Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patientsC Kawase, K Kawase, T Taniguchi, et al.
Ophthalmic Genetics|January 5, 2000
Exclusion of AR-CHED from the chromosome 20 region containing the PPMD and AD-CHED lociA B Kanis, A A Al-Rajhi, C M Taylor, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.
Genomics|April 1, 1991
The CEPH consortium linkage map of human chromosome 1N C Dracopoli, P O'Connell, T I Elsner, et al.
Human Molecular Genetics|April 18, 2000
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular developmentR S Smith, A Zabaleta, T Kume, et al.
American Journal of Human Genetics|March 1, 1990
Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome IqJ C Murray, D Y Nishimura, K H Buetow, et al.
Nature Genetics|June 10, 1998
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25D Y Nishimura, R E Swiderski, W L Alward, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Genome Research|March 7, 2001
Generation of a high-density rat EST mapT E Scheetz, M R Raymond, D Y Nishimura, et al.
Pageof 3