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X
Robevska, G. (Gorjana)
44  Ergebnisse:
Personensuche X
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1

COUP-TFII regulates early bipotential gonad signaling and c..:

Ferreira, Lucas G. A. ; Kizys, Marina M. L. ; Gama, Gabriel A. C....
Cell & Bioscience.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
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2

Generation of heterozygous (MCRIi030-A-1) and homozygous (M..:

Ferreira, Lucas G.A. ; Cabral-da-Silva, Mauricio C. ; Pachernegg, Svenja...
Stem Cell Research.  76 (2024)  - p. 103374 , 2024
Link: https://doi.org/10.1016/..
 
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3

Generation of heterozygous (MCRIi031-A-1) and homozygous (M..:

Pachernegg, Svenja ; Robevska, Gorjana ; G. A. Ferreira, Lucas...
Stem Cell Research.  79 (2024)  - p. 103484 , 2024
Link: https://doi.org/10.1016/..
 
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4

Deficiency of the mitochondrial ribosomal subunit, MRPL50, ..:

Bakhshalizadeh, Shabnam ; Hock, Daniella H. ; Siddall, Nicole A....
Human Genetics.  142 (2023)  7 - p. 879-907 , 2023
Link: https://doi.org/10.1007/..
 
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5

NR5A1 gene variants repress the ovarian-specific WNT signal..:

Knarston, I.M. (Ingrid M.) ; Robevska, G. (Gorjana) ; van den Bergen, J.A. (Jocelyn A)...
http://repub.eur.nl/pub/113017.  , 2018
Link: http://repub.eur.nl/pub/..
 
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6

Functional characterisation of novel NR5A1 variants reveals..:

Robevska, G. (Gorjana) ; Den Bergen, J.A. (Jocelyn A.) ; Ohnesorg, T. (Thomas)...
http://repub.eur.nl/pub/102764.  , 2017
Link: http://repub.eur.nl/pub/..
 
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7

Disorders of sex development: Insights from targeted gene s..:

Eggers, S. (Stefanie) ; Sadedin, S. (Simon) ; van den Bergen, J.A. (Jocelyn A.)...
http://repub.eur.nl/pub/94541.  , 2016
Link: http://repub.eur.nl/pub/..
 
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8

Additional file 1 of COUP-TFII regulates early bipotential ..:

Lucas G. A. Ferreira ; Marina M. L. Kizys ; Gabriel A. C. Gama...
doi:10.6084/m9.figshare.24946516.v1.  , 2024
Link: https://doi.org/10.6084/..
 
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9

COUP-TFII regulates early bipotential gonad signaling and c..:

Lucas G. A. Ferreira ; Marina M. L. Kizys ; Gabriel A. C. Gama...
https://doi.org/10.1186/s13578-023-01182-5.  , 2024
Link: https://doi.org/10.1186/..
 
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10

Deficiency of the mitochondrial ribosomal subunit, MRPL50, ..:

Bakhshalizadeh, Shabnam ; Hock, Daniella H ; Siddall, Nicole A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10329598/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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11

Biallelic FANCA variants detected in sisters with isolated ..:

Tucker, Elena J. ; Sharp, Michael F. ; Lokchine, Anna...
Clinical Genetics.  , 2024
Link: https://doi.org/10.1111/..
 
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12

Diverse genetic causes of amenorrhea in an ethnically homog..:

Bakhshalizadeh, Shabnam ; Afkhami, Fateme ; Bell, Katrina M....
Molecular and Cellular Endocrinology.  587 (2024)  - p. 112212 , 2024
Link: https://doi.org/10.1016/..
 
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13

A Human Homozygous HELQ Missense Variant Does Not Cause Pre..:

Bakhshalizadeh, Shabnam ; Bird, Anthony D. ; Sreenivasan, Rajini...
Genes.  15 (2024)  3 - p. 333 , 2024
Link: https://doi.org/10.3390/..
 
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14

Variants in SART3 cause a spliceosomopathy characterised by..:

Ayers, Katie L. ; Eggers, Stefanie ; Rollo, Ben N....
Nature Communications.  14 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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15

Author Correction: Variants in SART3 cause a spliceosomopat..:

Ayers, Katie L. ; Eggers, Stefanie ; Rollo, Ben N....
Nature Communications.  14 (2023)  1 - p. , 2023
Link: https://doi.org/10.1038/..
 
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