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PubPharm (50)
1
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
enthalten in:
Human molecular genetics
| 2013
von
Geister, K.
|
Brinkmeier, M.
|
Hsieh, M.
| +6
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2
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type
enthalten in:
Human molecular genetics
| 2012
von
Geister, K.
|
Brinkmeier, M.
|
Hsieh, M.
| +6
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3
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice
enthalten in:
Mammalian genome : official journal of the International Mammalian Genome Society
| 2007
von
Karolyi, I.
|
Dootz, G.
|
Halsey, K.
| +7
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4
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice
enthalten in:
Mammalian genome
| 2007
von
Karolyi, I.
|
Dootz, G.
|
Halsey, K.
| +7
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5
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice
enthalten in:
Mammalian genome
| 2007
von
Karolyi, I.
|
Dootz, G.
|
Halsey, K.
| +7
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6
Age-related changes in cochlear gene expression in normal and shaker 2 mice
enthalten in:
Journal of the Association for Research in Otolaryngology : JARO
| 2006
von
Gong, T.
|
Karolyi, I.
|
Macdonald, J.
| +5
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7
Age-Related Changes in Cochlear Gene Expression In Normal and Shaker 2 Mice
enthalten in:
Journal of the Association for Research in Otolaryngology
| 2006
von
Gong, T.
|
Karolyi, I.
|
MacDonald, J.
| +5
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8
Age-Related Changes in Cochlear Gene Expression In Normal and Shaker 2 Mice
enthalten in:
Journal of the Association for Research in Otolaryngology
| 2006
von
Gong, T.
|
Karolyi, I.
|
MacDonald, J.
| +5
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9
Age-Related Changes in Cochlear Gene Expression In Normal and Shaker 2 Mice
enthalten in:
Journal of the Association for Research in Otolaryngology
| 2006
von
Gong, T.
|
Karolyi, I.
|
MacDonald, J.
| +5
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10
Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice
enthalten in:
Hearing research
| 2006
von
Kanzaki, S.
|
Beyer, L.
|
Karolyi, I.
| +5
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SYPHILIS/diagnosis
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3
9015-71-8
3
Corticotropin-Releasing Hormone
3
EC 3.6.4.1
3
Myosins
3
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bone
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collagen
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gene expression profiling
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myosin XV
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6158TKW0C5
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Carrier Proteins
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Congenital Hypothyroidism
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Genetic Markers
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Hearing Impairment
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Hearing Loss
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