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A Strategy to Enhance Secretion of Extracellular Matrix Components by Stem Cells: Relevance to Tissue Engineering. [electronic resource] by
- Krishnamoorthy, Navaneethakrishnan
- Tseng, Yuan-Tsan
- Gajendrarao, Poornima
- Sarathchandra, Padmini
- McCormack, Ann
- Carubelli, Ivan
- Sohier, Jerome
- Latif, Najma
- Chester, Adrian H
- Yacoub, Magdi H
Producer: 20181105
In:
Tissue engineering. Part A vol. 24
Availability: No items available.
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14.
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Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interaction. [electronic resource] by
- Da'as, Sahar I
- Fakhro, Khalid
- Thanassoulas, Angelos
- Krishnamoorthy, Navaneethakrishnan
- Saleh, Alaaeldin
- Calver, Brian L
- Safieh-Garabedian, Bared
- Toft, Egon
- Nounesis, George
- Lai, F Anthony
- Nomikos, Michail
Producer: 20190528
In:
The Biochemical journal vol. 475
Availability: No items available.
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15.
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Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families. [electronic resource] by
- Alkowari, Moza K
- Vozzi, Diego
- Bhagat, Shruti
- Krishnamoorthy, Navaneethakrishnan
- Morgan, Anna
- Hayder, Yousra
- Logendra, Barathy
- Najjar, Nehal
- Gandin, Ilaria
- Gasparini, Paolo
- Badii, Ramin
- Girotto, Giorgia
- Abdulhadi, Khalid
Producer: 20170928
In:
Mutation research vol. 800-802
Availability: No items available.
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16.
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Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia? [electronic resource] by
- Sanoudou, Despina
- Kolokathis, Fotis
- Arvanitis, Demetris
- Al-Shafai, Kholoud
- Krishnamoorthy, Navaneethakrishnan
- Buchan, Rachel J
- Walsh, Roddy
- Tsiapras, Dimitris
- Barton, Paul Jr
- Cook, Stuart A
- Kremastinos, Dimitrios
- Yacoub, Magdi
Producer: 20151116
In:
Global cardiology science & practice vol. 2015
Availability: No items available.
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17.
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Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. [electronic resource] by
- Morgan, Anna
- Vuckovic, Dragana
- Krishnamoorthy, Navaneethakrishnan
- Rubinato, Elisa
- Ambrosetti, Umberto
- Castorina, Pierangela
- Franzè, Annamaria
- Vozzi, Diego
- La Bianca, Martina
- Cappellani, Stefania
- Di Stazio, Mariateresa
- Gasparini, Paolo
- Girotto, Giorgia
Producer: 20190411
In:
European journal of human genetics : EJHG vol. 27
Availability: No items available.
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18.
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Two patients with Canavan disease and structural modeling of a novel mutation. [electronic resource] by
- Zaki, Osama K
- Krishnamoorthy, Navaneethakrishnan
- El Abd, Heba S
- Harche, Soumaya A
- Mattar, Reem A
- Al Disi, Rana S
- Nofal, Mariam Y
- El Bekay, Rajaa
- Ahmed, Khalid A
- George Priya Doss, C
- Zayed, Hatem
Producer: 20180131
In:
Metabolic brain disease vol. 32
Availability: No items available.
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19.
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In silico and in vivo models for Qatari-specific classical homocystinuria as basis for development of novel therapies. [electronic resource] by
- Ismail, Hesham M
- Krishnamoorthy, Navaneethakrishnan
- Al-Dewik, Nader
- Zayed, Hatem
- Mohamed, Nura A
- Giacomo, Valeria Di
- Gupta, Sapna
- Häberle, Johannes
- Thöny, Beat
- Blom, Henk J
- Kruger, Waren D
- Ben-Omran, Tawfeg
- Nasrallah, Gheyath K
Producer: 20200309
In:
Human mutation vol. 40
Availability: No items available.
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