Search Results - "Zargar, N."
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A layered electrospun and woven surgical scaffold to enhance endogenous tendon repair
Published in Acta biomaterialia (01-10-2015)“…[Display omitted] Surgical reattachments of tendon to bone in the rotator cuff are reported to fail in around 40% of cases. There are no adequate solutions to…”
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Apoptosis and cell cycle regulatory effects of adenosine by modulation of GLI‐1 and ERK1/2 pathways in CD44+ and CD24− breast cancer stem cells
Published in Cell proliferation (01-08-2017)“…Objectives Breast cancer stem cells (CSCs) are a small population of tumour cells with the ability of self‐renewal and resistance to chemotherapy. Targeting…”
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Mechanical properties of all-suture anchors for rotator cuff repair
Published in Bone & joint research (01-02-2017)“…All-suture anchors are increasingly used in rotator cuff repair procedures. Potential benefits include decreased bone damage. However, there is limited…”
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Congenital Erythropoietic Porphyria: A Rare Inherited Disorder
Published in Curēus (Palo Alto, CA) (05-03-2024)“…Congenital erythropoietic porphyria (CEP), also known as Gunther's disease, is an uncommon autosomal recessive disorder caused by a mutation in the…”
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Apoptosis and cell cycle regulatory effects of adenosine by modulation of GLI ‐1 and ERK 1/2 pathways in CD 44 + and CD 24 − breast cancer stem cells
Published in Cell proliferation (01-08-2017)“…Abstract Objectives Breast cancer stem cells ( CSC s) are a small population of tumour cells with the ability of self‐renewal and resistance to chemotherapy…”
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6
Laparoscopic repair of a congenital diaphragmatic hernia
Published in Pediatric surgery international (01-09-2002)“…The standard treatment of congenital diaphragmatic hernia is by open operation. We have successfully performed a laparoscopic repair in an asymptomatic…”
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Congenital Erythropoietic Porphyria: A Rare Inherited Disorder
Published in Cureus (01-03-2024)“…Congenital erythropoietic porphyria (CEP), also known as Gunther's disease, is an uncommon autosomal recessive disorder caused by a mutation in the…”
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