E-LIB Suche - Ergebnisse für: Dil, Sobia

1

A homozygous ARMC3 splicing variant causes asthenozoospermi..:

Rahim, Fazal ; Tao, Liu ; Khan, Khalid...
Clinical Genetics. , 2024

Link: https://doi.org/10.1111/..

2

A novel homozygous TSGA10 missense variant causes acephalic..:

Khan, Khalid ; Zhang, Xiangjun ; Dil, Sobia...
Basic and Clinical Andrology. 34 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

3

A novel NPHP4 homozygous missense variant identified in inf..:

Ali, Asim ; Unar, Ahsanullah ; Muhammad, Zubair...
Journal of Assisted Reproduction and Genetics. , 2023

Link: https://doi.org/10.1007/..

4

Cornichon protein CNIH4 is not essential for mice gametogen..:

Dil, Sobia ; Ye, Jingwei ; Ma, Hui...
Developmental Biology. 496 (2023) - p. 15-23 , 2023

Link: https://doi.org/10.1016/..

5

A homozygous KASH5 frameshift mutation causes diminished ov..:

Hou, Xiaoning ; Zeb, Aurang ; Dil, Sobia...
Frontiers in Endocrinology. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

6

Loss-of-function mutations in CFAP57 cause multiple morphol..:

Ma, Ao ; Zhou, Jianteng ; Ali, Haider...
JCI Insight. 8 (2023) 3 - p. , 2023

Link: https://doi.org/10.1172/..

7

Testis-specific fascin component FSCN3 is dispensable for m..:

Ali, Haider ; Unar, Ahsanullah ; Dil, Sobia...
Molecular Biology Reports. 49 (2022) 7 - p. 6261-6268 , 2022

Link: https://doi.org/10.1007/..

8

Homozygous mutations in C14orf39/SIX6OS1 cause non-obstruct..:

Fan, Suixing ; Jiao, Yuying ; Khan, Ranjha...
The American Journal of Human Genetics. 109 (2022) 7 - p. 1343 , 2022

Link: https://doi.org/10.1016/..

9

In silico analysis of a novel pathogenic variant c.7G > A i..:

Ali, Haider ; Unar, Ahsanullah ; Zubair, Muhammad...
Molecular Genetics and Genomics. 297 (2022) 3 - p. 719-730 , 2022

Link: https://doi.org/10.1007/..

10

A novel stop-gain mutation in ARMC2 is associated with mult..:

Khan, Ihsan ; Dil, Sobia ; Zhang, Huan...
Reproductive BioMedicine Online. 43 (2021) 5 - p. 913-919 , 2021

Link: https://doi.org/10.1016/..

11

The Molecular Mechanism of Sex Hormones on Sertoli Cell Dev..:

Shah, Wasim ; Khan, Ranjha ; Shah, Basit...
Frontiers in Endocrinology. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

12

Exonuclease 5 is dispensable for meiotic progression and ma..:

Zaman, Qumar ; Khan, Ranjha ; Hameed, Uzma...
Gene. 769 (2021) - p. 145254 , 2021

Link: https://doi.org/10.1016/..

13

Novel frameshift mutation in STK33 is associated with asthe..:

Ma, Hui ; Zhang, Beibei ; Khan, Asad...
Human Molecular Genetics. 30 (2021) 21 - p. 1977-1984 , 2021

Link: https://doi.org/10.1093/..

14

Homozygous mutations in C14orf39/SIX6OS1 cause non-obstruct..:

Fan, Suixing ; Jiao, Yuying ; Khan, Ranjha...
The American Journal of Human Genetics. 108 (2021) 2 - p. 324-336 , 2021

Link: https://doi.org/10.1016/..

15

The evolutionarily conserved gene, Fam114a2, is dispensable..:

Khan, Asad ; Yuewen, Wang ; Dil, Sobia...
Reproductive Biology. 21 (2021) 3 - p. 100531 , 2021

Link: https://doi.org/10.1016/..