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/vufind/Search/Results?lookfor=%22WDR62%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
/vufind/Search/Results?lookfor=%22WDR62%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
Search /vufind/Search2/Results?lookfor=%22WDR62%22&type=Subject&sort=year%2C+publishDateDaySort_date+desc%2C+id
PubPharm (110)
1
Autosomal recessive primary microcephaly type 2 associated with a novel WDR62 splicing variant that disrupts the expression of the functional transcript
enthalten in:
Frontiers in neurology
| 2024
von
Chen, H.
|
Zheng, Y.
|
Wu, H.
| +4
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2
Autosomal recessive primary microcephaly type 2 associated with a novel WDR62 splicing variant that disrupts the expression of the functional transcript
in:
Frontiers in Neurology
| 2024
von
Haizhu Chen
|
Haizhu Chen
|
Ying Zheng
| +11
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3
WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice
enthalten in:
Neuroscience bulletin
| 2023
von
Xu, D.
|
Zhi, Y.
|
Liu, X.
| +7
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4
Genetic Primary Microcephalies : When Centrosome Dysfunction Dictates Brain and Body Size
enthalten in:
Cells
| 2023
von
Farcy, S.
|
Hachour, H.
|
Bahi-Buisson, N.
| +1
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5
Microcephaly-associated protein WDR62 shuttles from the Golgi apparatus to the spindle poles in human neural progenitors
enthalten in:
eLife
| 2023
von
Dell'Amico, C.
|
Angulo Salavarria, M.
|
Takeo, Y.
| +7
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6
Clinical and genetic analyses in syndromic intellectual disability with primary microcephaly reveal biallelic and de novo variants in patients with parental consanguinity
enthalten in:
Genes & genomics
| 2023
von
Mercan, S.
|
Akcakaya, N.
|
Salman, B.
| +3
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7
Autosomal Recessive Primary Microcephaly (MCPH) and Novel Pathogenic Variants in ASPM and WDR62 Genes
enthalten in:
Molecular syndromology
| 2022
von
Bolat, H.
|
Sağer, S.
|
Türkyılmaz, A.
| +5
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8
WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice
enthalten in:
Neuroscience bulletin
| 2022
von
Xu, D.
|
Zhi, Y.
|
Liu, X.
| +7
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9
WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice
enthalten in:
Neuroscience bulletin
| 2022
von
Xu, D.
|
Zhi, Y.
|
Liu, X.
| +7
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10
Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly
enthalten in:
Irish journal of medical science
| 2022
von
Aryan, H.
|
Zokaei, S.
|
Farhud, D.
| +6
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American journal of medical genetics. Part A
4
BMC medical genetics
4
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4
Irish journal of medical science
3
BMC neurology
3
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Thema
84
Journal Article
78
Nerve Tissue Proteins
73
Cell Cycle Proteins
58
WDR62 protein, human
47
Research Support, Non-U.S. Gov't
43
WDR62
16
Microtubule-Associated Proteins
15
Research Support, N.I.H., Extramural
14
WDR62 protein, mouse
12
Case Reports
12
EC 2.7.11.1
10
EC 2.7.11.24
10
MCPH
10
microcephaly
9
Microcephaly
7
Aurora Kinase A
7
Drosophila Proteins
7
Review
7
Wdr62 protein, Drosophila
7
Whole-exome sequencing
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Erscheinungszeitraum
41
2020-
69
2010-2019
Erscheinungsjahr(e)
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Sprache
109
Englisch
1
Russisch
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