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	1.	Cellularized biosynthetic microhydrogel polymers for intravascular liver tissue regeneration therapy. [electronic resource] by Saadi, Tarek Nayshool, Omri Carmel, Julie Ariche, Arie Bramnik, Zakhar Mironi-Harpaz, Iris Seliktar, Dror Baruch, Yaacov Producer: 20150701 In: Tissue engineering. Part A vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	OPTN 691_692insAG is a founder mutation causing recessive ALS and increased risk in heterozygotes. [electronic resource] by Goldstein, Orly Nayshool, Omri Nefussy, Beatrice Traynor, Bryan J Renton, Alan E Gana-Weisz, Mali Drory, Vivian E Orr-Urtreger, Avi Producer: 20160622 In: Neurology vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	High frequency of C9orf72 hexanucleotide repeat expansion in amyotrophic lateral sclerosis patients from two founder populations sharing the same risk haplotype. [electronic resource] by Goldstein, Orly Gana-Weisz, Mali Nefussy, Beatrice Vainer, Batel Nayshool, Omri Bar-Shira, Anat Traynor, Bryan J Drory, Vivian E Orr-Urtreger, Avi Producer: 20180927 In: Neurobiology of aging vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	BRPF1-associated intellectual disability, ptosis, and facial dysmorphism in a multiplex family. [electronic resource] by Pode-Shakked, Naomi Barel, Ortal Pode-Shakked, Ben Eliyahu, Aviva Singer, Amihood Nayshool, Omri Kol, Nitzan Raas-Rothschild, Annick Pras, Elon Shohat, Mordechai Producer: 20200623 In: Molecular genetics & genomic medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics. [electronic resource] by Goldstein, Orly Kedmi, Merav Gana-Weisz, Mali Twito, Shir Nefussy, Beatrice Vainer, Batel Fainmesser, Yaara Abraham, Alon Nayshool, Omri Orr-Urtreger, Avi Drory, Vivian E Producer: 20200817 In: Journal of the neurological sciences vol. 402 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Reduced Function and Diversity of T Cell Repertoire and Distinct Clinical Course in Patients With [electronic resource] by Lev, Atar Simon, Amos J Barel, Ortal Eyal, Eran Glick-Saar, Efrat Nayshool, Omri Birk, Ohad Stauber, Tali Hochberg, Amit Broides, Arnon Almashanu, Shlomo Hendel, Ayal Lee, Yu Nee Somech, Raz Producer: 20200928 In: Frontiers in immunology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A founder truncating variant in GDF1 causes autosomal-recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds. [electronic resource] by Marek-Yagel, Dina Bolkier, Yoav Barel, Ortal Vardi, Amir Mishali, David Katz, Uriel Salem, Yishay Abudi, Shachar Nayshool, Omri Kol, Nitzan Raas-Rothschild, Annick Rechavi, Gideon Anikster, Yair Pode-Shakked, Ben Producer: 20210112 In: American journal of medical genetics. Part A vol. 182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)