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BMC Genetics|February 15, 2001

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J miceM G Anderson, R S Smith, O V Savinova, et al.

Nature|May 11, 1995

Male-female differences in fertility and blood pressure in ACE-deficient miceJ H Krege, S W John, L L Langenbach, et al.

Molecular and Cellular Biology|October 18, 2001

Targeted Disruption of the Myocilin Gene (Myoc) Suggests that Human Glaucoma-Causing Mutations Are Gain of FunctionB S Kim, O V Savinova, M V Reedy, et al.

Nature Genetics|April 7, 1999

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J miceB Chang, R S Smith, N L Hawes, 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.

BMC Genetics|November 28, 2001

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressureB Chang, R S Smith, M Peters, et al.

Human Molecular Genetics|February 22, 2001

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid depositionZ Chen, A C Karaplis, S L Ackerman, et al.

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Showing results (21-30 of 27) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 27 results.

BMC Genetics|February 15, 2001

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J miceM G Anderson, R S Smith, O V Savinova, et al.

Nature|May 11, 1995

Male-female differences in fertility and blood pressure in ACE-deficient miceJ H Krege, S W John, L L Langenbach, et al.

Molecular and Cellular Biology|October 18, 2001

Targeted Disruption of the Myocilin Gene (Myoc) Suggests that Human Glaucoma-Causing Mutations Are Gain of FunctionB S Kim, O V Savinova, M V Reedy, et al.

Nature Genetics|April 7, 1999

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J miceB Chang, R S Smith, N L Hawes, 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.

BMC Genetics|November 28, 2001

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressureB Chang, R S Smith, M Peters, et al.

Human Molecular Genetics|February 22, 2001

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid depositionZ Chen, A C Karaplis, S L Ackerman, et al.

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