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Search Results - Nishina, P.M
Search Results - Nishina, P.M
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Disruption in murine Eml1 perturbs retinal lamination during early development
by
Collin, G. B.
,
Won, J.
,
Krebs, M. P.
,
Hicks, W. J.
,
Charette, J. R.
,
Naggert, J. K.
,
Nishina, P. M.
Published in
Scientific reports
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Alms1-disrupted mice recapitulate human Alström syndrome
by
Collin, G B
,
Cyr, E
,
Bronson, R
,
Marshall, J D
,
Gifford, E J
,
Hicks, W
,
Murray, S A
,
Zheng, Q Y
,
Smith, R S
,
Nishina, P M
,
Naggert, J K
Published in
Human molecular genetics
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Lith1, a major gene affecting cholesterol gallstone formation among inbred strains of mice
by
Khanuja, Bhupinder
,
Cheah, Yin-Chai
,
Hunt, Mark
,
Nishina, Patsy M.
,
David Q.-H. Wang
,
Chen, Harry W.
,
Billheimer, Jeffrey T.
,
Carey, Martin C.
,
Paigen, Beverly
Published in
Proceedings of the National Academy of Sciences - PNAS
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Synthetic low and high fat diets for the study of atherosclerosis in the mouse
by
Nishina, PM
,
Verstuyft, J
,
Paigen, B
Published in
Journal of lipid research
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Effects of dietary fats from animal and plant sources on diet-induced fatty streak lesions in C57BL/6J mice
by
Nishina, P.M
,
Lowe, S
,
Verstuyft, J
,
Naggert, J.K
,
Kuypers, F.A
,
Paigen, B
Published in
Journal of lipid research
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Alström syndrome : further evidence for linkage to human chromosome 2p13
by
COLLIN, G. B
,
MARSHALL, J. D
,
BOERKOEL, C. F
,
LEVIN, A. V
,
WEKSBERG, R
,
GREENBERG, J
,
MICHAUD, J. L
,
NAGGERT, J. K
,
NISHINA, P. M
Published in
Human genetics
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Alms1-disrupted mice recapitulate human Alström syndrome
by
Collin, G.B.
,
Cyr, E.
,
Bronson, R.
,
Marshall, J.D.
,
Gifford, E.J.
,
Hicks, W.
,
Murray, S.A.
,
Zheng, Q.Y.
,
Smith, R.S.
,
Nishina, P.M.
,
Naggert, J.K.
Published in
Human molecular genetics
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Alström syndrome: further evidence for linkage to human chromosome 2p13
by
Collin, G.B.
,
Marshall, J.D.
,
Boerkoel, C.F.
,
Levin, A.V.
,
Weksberg, R.
,
Greenberg, J.
,
Michaud, J.L.
,
Naggert, J.K.
,
Nishina, P.M.
Published in
Human genetics
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PCR assay for a polymorphic PvuII site in the LPL gene
by
JOHNSON, J. P
,
NISHINA, P. M
,
NAGGERT, J. K
Published in
Nucleic acids research
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PCR assay for a polymorphic Pvu ll site in the LPL gene
by
Johnson, J.P.
,
Nishina, P.M.
,
Naggert, J.K.
Published in
Nucleic acids research
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Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice
by
Boldt, Karsten
,
Mans, Dorus A
,
Won, Jungyeon
,
van Reeuwijk, Jeroen
,
Vogt, Andreas
,
Kinkl, Norbert
,
Letteboer, Stef J F
,
Hicks, Wanda L
,
Hurd, Ron E
,
Naggert, Jürgen K
,
Texier, Yves
,
den Hollander, Anneke I
,
Koenekoop, Robert K
,
Bennett, Jean
,
Cremers, Frans P M
,
Gloeckner, Christian J
,
Nishina, Patsy M
,
Roepman, Ronald
,
Ueffing, Marius
Published in
The Journal of clinical investigation
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Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness
by
Song, Ji Yun
,
Aravand, Puya
,
Nikonov, Sergei
,
Leo, Lanfranco
,
Lyubarsky, Arkady
,
Bennicelli, Jeannette L.
,
Pan, Jieyan
,
Wei, Zhangyong
,
Shpylchak, Ivan
,
Herrera, Pamela
,
Bennett, Daniel J.
,
Commins, Nicoletta
,
Maguire, Albert M.
,
Pham, Jennifer
,
den Hollander, Anneke I.
,
Cremers, Frans P.M.
,
Koenekoop, Robert K.
,
Roepman, Ronald
,
Nishina, Patsy
,
Zhou, Shangzhen
,
Pan, Wei
,
Ying, Gui-shuang
,
Aleman, Tomas S.
,
de Melo, Jimmy
,
McNamara, Ilan
,
Sun, Junwei
,
Mills, Jason
,
Bennett, Jean
Published in
Molecular therapy
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