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/vufind/Search/Results?lookfor=%22Cavarocchi%2C+Emma%22&type=Person&sort=year
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PubPharm (13)
1
CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans
enthalten in:
Clinical genetics
| 2024
von
Jreijiri, F.
|
Cavarocchi, E.
|
Amiri-Yekta, A.
| +9
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2
Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans
enthalten in:
iScience
| 2023
von
Cavarocchi, E.
|
Sayou, C.
|
Lorès, P.
| +12
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3
Sperm Ion Transporters and Channels in Human Asthenozoospermia : Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives
enthalten in:
International journal of molecular sciences
| 2022
von
Cavarocchi, E.
|
Whitfield, M.
|
Saez, F.
| +1
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4
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
ErratumIn: Hum Genet. 2021 Mar 26;:. - PMID 33770252
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5
Correction to : A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
ErratumFor: Hum Genet. 2021 Jul;140(7):1031-1043. - PMID 33689014
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6
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility
enthalten in:
Clinical genetics
| 2021
von
Cavarocchi, E.
|
Whitfield, M.
|
Chargui, A.
| +10
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7
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
Wird geladen...
8
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
Wird geladen...
9
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
Wird geladen...
10
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome
enthalten in:
Human genetics
| 2021
von
Lorès, P.
|
Kherraf, Z.
|
Amiri-Yekta, A.
| +17
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1
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asthenozoospermia
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gene mutation
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ion channel
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male infertility
1
CCDC65
1
CCDC65 protein, human
1
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Cytoskeletal Proteins
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Dyneins
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EC 3.6.4.2
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IFT74 protein, human
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2021
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