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/vufind/Search/Results?lookfor=%22X+chromosome+inactivation%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22X+chromosome+inactivation%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
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PubPharm (842)
1
Escape from X-chromosome inactivation and sex differences in Alzheimer's disease
enthalten in:
Reviews in the neurosciences
| 2024
von
Song, Q.
|
Zhao, K.
|
Huang, S.
| +2
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2
Qualitative and quantitative analysis of MED12 c.887G>A causing both missense and splicing variants in X-linked Ohdo syndrome
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Togi, S.
|
Ura, H.
|
Niida, Y.
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3
Development and application of haploid embryonic stem cells
enthalten in:
Stem cell research & therapy
| 2024
von
Wang, H.
|
Ma, X.
|
Guo, Y.
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4
Development and application of haploid embryonic stem cells
enthalten in:
Stem cell research & therapy
| 2024
von
Wang, H.
|
Ma, X.
|
Guo, Y.
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5
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
enthalten in:
BMC genomics
| 2024
von
Fadra, N.
|
Schultz-Rogers, L.
|
Chanana, P.
| +9
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6
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
enthalten in:
BMC genomics
| 2024
von
Fadra, N.
|
Schultz-Rogers, L.
|
Chanana, P.
| +9
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7
Unraveling the role of Xist in X chromosome inactivation : insights from rabbit model and deletion analysis of exons and repeat A
enthalten in:
Cellular and molecular life sciences : CMLS
| 2024
von
Liang, M.
|
Zhang, L.
|
Lai, L.
| +1
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8
Unraveling the role of Xist in X chromosome inactivation: insights from rabbit model and deletion analysis of exons and repeat A
enthalten in:
Cellular and molecular life sciences
| 2024
von
Liang, M.
|
Zhang, L.
|
Lai, L.
| +1
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9
Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients
enthalten in:
Molecular genetics and genomics : MGG
| 2024
von
Yang, M.
|
Peng, L.
|
Lv, L.
| +4
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10
Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients
enthalten in:
Molecular genetics and genomics
| 2024
von
Yang, M.
|
Peng, L.
|
Lv, L.
| +4
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Epigenetics & chromatin
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X chromosome inactivation
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81
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70
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epigenetics
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34
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34
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dosage compensation
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Heterochromatin
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