E-LIB Suche - Ergebnisse für: Noa Henig

1

MSL2 variants lead to a neurodevelopmental syndrome with la..:

Karayol, Remzi ; Borroto, Maria Carla ; Haghshenas, Sadegheh...
The American Journal of Human Genetics. 111 (2024) 7 - p. 1330-1351 , 2024

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

2

NEBNext Direct: A Novel, Rapid, Hybridization‐Based Approac..:

Emerman, Amy B. ; Bowman, Sarah K. ; Barry, Andrew...
Current Protocols in Molecular Biology. 119 (2017) 1 - p. , 2017

Link: https://doi.org/10.1002/..

3

Interferon-Beta Induces Distinct Gene Expression Response P..:

Henig, Noa ; Avidan, Nili ; Mandel, Ilana...
PLoS ONE. 8 (2013) 4 - p. e62366 , 2013

Link: https://doi.org/10.1371/..

4

Monoallelic variation in DHX9, the gene encoding the DExH-b..:

Calame, Daniel G. ; Guo, Tianyu ; Wang, Chen...
The American Journal of Human Genetics. 110 (2023) 8 - p. 1394-1413 , 2023

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

5

Biallelic loss of EMC10 leads to mild to severe intellectua..:

Kaiyrzhanov, Rauan ; Rocca, Clarissa ; Suri, Mohnish...
Annals of Clinical and Translational Neurology. 9 (2022) 7 - p. 1080-1089 , 2022

Link: https://doi.org/10.1002/..

6

Non‐immune hydrops fetalis caused by PIEZO1 compound hetero..:

Reytan, Sivan ; Zunz Henig, Noa ; Yinon, Yoav...
Prenatal Diagnosis. 42 (2022) 7 - p. 890-893 , 2022

Link: https://doi.org/10.1002/..

7

eP345: Community data-driven approach for generating cross-..:

Einhorn, Yaron ; Einhorn, Moshe ; Yaron, Yuval...
Genetics in Medicine. 24 (2022) 3 - p. S216 , 2022

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

8

CD55-deficiency in Jews of Bukharan descent is caused by th..:

Kurolap, Alina ; Hagin, David ; Freund, Tal...
Human Genetics. 142 (2022) 5 - p. 683-690 , 2022

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

9

Interferon-beta induces distinct gene expression response p..:

Noa Henig ; Nili Avidan ; Ilana Mandel...
http://europepmc.org/articles/PMC3633862?pdf=render. , 2013

Link: https://doi.org/10.1371/..

10

Translation towards personalized medicine in Multiple Scler..:

Miller, Ariel ; Avidan, Nili ; Tzunz-Henig, Noa...
Journal of the Neurological Sciences. 274 (2008) 1-2 - p. 68-75 , 2008

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

11

Biallelic loss of EMC10 leads to mild to severe intellectua..:

Rauan Kaiyrzhanov ; Clarissa Rocca ; Mohnish Suri...
https://doi.org/10.1002/acn3.51602. , 2022

Link: https://doi.org/10.1002/..

12

De novo variants in ATP2B1 lead to neurodevelopmental delay..:

RAHIMI, Meer Jacob ; URBAN, Nicole ; WEGLER, Meret...
1537-6605. , 2022

Link: https://oskar-bordeaux.f..

13

De novo variants in ATP2B1 lead to neurodevelopmental delay:

Rahimi, Meer Jacob ; Urban, Nicole ; Wegler, Meret...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2022.03.009. , 2022

Link: https://hal.science/hal-..

14

Biallelic loss of EMC10 leads to mild to severe intellectua..:

Kaiyrzhanov, Rauan ; Rocca, Clarissa ; Suri, Mohnish...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9268894/. , 2022

Link: http://www.ncbi.nlm.nih...

15

Bone marrow blast elimination by the fifth day of 7 + 3 ind..:

Ofran, Yishai ; Hayun, Michal ; Leiba, Ronit...
American Journal of Hematology. 95 (2019) 1 - p. , 2019

Link: https://doi.org/10.1002/..