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/vufind/Search/Results?lookfor=%22Sreenivasan%2C+Rajini%22&type=Person&sort=year
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PubPharm (44)
1
A Human Homozygous HELQ Missense Variant Does Not Cause Premature Ovarian Insufficiency in a Mouse Model
enthalten in:
Genes
| 2024
von
Bakhshalizadeh, S.
|
Bird, A.
|
Sreenivasan, R.
| +12
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2
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency
enthalten in:
Human genetics
| 2023
von
Bakhshalizadeh, S.
|
Hock, D.
|
Siddall, N.
| +23
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3
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency
enthalten in:
Human genetics
| 2023
von
Bakhshalizadeh, S.
|
Hock, D.
|
Siddall, N.
| +23
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4
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency
enthalten in:
Human genetics
| 2023
von
Bakhshalizadeh, S.
|
Hock, D.
|
Siddall, N.
| +23
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5
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiency
enthalten in:
Human genetics
| 2023
von
Bakhshalizadeh, S.
|
Hock, D.
|
Siddall, N.
| +23
Wird geladen...
6
Generation and mutational analysis of a transgenic mouse model of human SRY
enthalten in:
bioRxiv.org
| 2022
von
Thomson, E.
|
Zhao, L.
|
Chen, Y.
| +9
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7
Premature Ovarian Insufficiency in CLPB Deficiency : Transcriptomic, Proteomic and Phenotypic Insights
enthalten in:
The Journal of clinical endocrinology and metabolism
| 2022
von
Tucker, E.
|
Baker, M.
|
Hock, D.
| +23
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8
Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency
enthalten in:
Human molecular genetics
| 2022
von
Nakagawa, R.
|
Takasawa, K.
|
Gau, M.
| +17
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9
Whole exome sequencing reveals copy number variants in individuals with disorders of sex development
enthalten in:
Molecular and cellular endocrinology
| 2022
von
Sreenivasan, R.
|
Bell, K.
|
van den Bergen, J.
| +9
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10
Generation and mutational analysis of a transgenic mouse model of human SRY
enthalten in:
Human mutation
| 2022
von
Thomson, E.
|
Zhao, L.
|
Chen, Y.
| +9
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SOX9 Transcription Factor
4
SOX9 protein, human
4
Sex-Determining Region Y Protein
3
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3
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enhancer
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premature ovarian insufficiency
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speciation
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NR5A1 protein, human
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2010-2019
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2000-2009
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