advertisement
Human Molecular Genetics 40
Showing records 1 to 25 | Display all abstracts in Human Molecular Genetics60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Pfirrmann T
Human Molecular Genetics 2015; 24: 3119-3132
60591 Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Joe MK
Human Molecular Genetics 2015; 24: 3322-3334
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Springelkamp H
Human Molecular Genetics 2015; 24: 2689-2699
60140 Structural basis for misfolding in myocilin-associated glaucoma
Donegan RK; Hill SE
Human Molecular Genetics 2015; 24: 2111-2124
60591 Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Nakaya N
Human Molecular Genetics 2015; 24: 3322-3334
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Emmerich D
Human Molecular Genetics 2015; 24: 3119-3132
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Iglesias AI
Human Molecular Genetics 2015; 24: 2689-2699
60591 Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Abu-Asab M
Human Molecular Genetics 2015; 24: 3322-3334
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Cuellar-Partida G
Human Molecular Genetics 2015; 24: 2689-2699
60140 Structural basis for misfolding in myocilin-associated glaucoma
Freeman DM
Human Molecular Genetics 2015; 24: 2111-2124
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Ruokonen P
Human Molecular Genetics 2015; 24: 3119-3132
60140 Structural basis for misfolding in myocilin-associated glaucoma
Nguyen E
Human Molecular Genetics 2015; 24: 2111-2124
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Quandt D
Human Molecular Genetics 2015; 24: 3119-3132
60591 Mutated myocilin and heterozygous Sod2 deficiency act synergistically in a mouse model of open-angle glaucoma
Tomarev SI
Human Molecular Genetics 2015; 24: 3322-3334
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Amin N; Burdon KP
Human Molecular Genetics 2015; 24: 2689-2699
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Buchen R
Human Molecular Genetics 2015; 24: 3119-3132
60140 Structural basis for misfolding in myocilin-associated glaucoma
Orwig SD
Human Molecular Genetics 2015; 24: 2111-2124
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Fischer-Zirnsak B
Human Molecular Genetics 2015; 24: 3119-3132
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
van Leeuwen EM
Human Molecular Genetics 2015; 24: 2689-2699
60140 Structural basis for misfolding in myocilin-associated glaucoma
Turnage KC; Lieberman RL
Human Molecular Genetics 2015; 24: 2111-2124
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Gharahkhani P
Human Molecular Genetics 2015; 24: 2689-2699
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Hecht J; Krawitz P
Human Molecular Genetics 2015; 24: 3119-3132
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Mishra A
Human Molecular Genetics 2015; 24: 2689-2699
60530 Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model
Meyer P
Human Molecular Genetics 2015; 24: 3119-3132
60375 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
van der Lee SJ; Hewitt AW
Human Molecular Genetics 2015; 24: 2689-2699
