Hasil Pencarian - Jia Nee Foo

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  1. 1
    Synaptic Vesicle Glycoprotein 2C: a role in Parkinson’s disease

    Synaptic Vesicle Glycoprotein 2C: a role in Parkinson’s disease oleh Chu Hua Chang, Chu Hua Chang, Kah Leong Lim, Kah Leong Lim, Jia Nee Foo, Jia Nee Foo

    Diterbitkan 2024-09-01
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  2. 2
    Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult Relationships

    Recalled Parental Bonding Interacts with Oxytocin Receptor Gene Polymorphism in Modulating Anxiety and Avoidance in Adult Relationships oleh Ilaria Cataldo, Andrea Bonassi, Bruno Lepri, Jia Nee Foo, Peipei Setoh, Gianluca Esposito

    Diterbitkan 2021-04-01
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  3. 3
    Gene–Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time

    Gene–Environment Interactions in Face Categorization: Oxytocin Receptor Genotype x Childcare Experience Shortens Reaction Time oleh Michelle Jin Yee Neoh, Peipei Setoh, Andrea Bizzego, Moses Tandiono, Moses Tandiono, Jia Nee Foo, Jia Nee Foo, Albert Lee, Marc H. Bornstein, Marc H. Bornstein, Marc H. Bornstein, Gianluca Esposito

    Diterbitkan 2022-06-01
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  4. 4
    A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family

    A Novel Homozygous Frameshift Variant in XYLT2 Causes Spondyloocular Syndrome in a Consanguineous Pakistani Family oleh Mehran Kausar, Mehran Kausar, Mehran Kausar, Elaine Guo Yan Chew, Elaine Guo Yan Chew, Hazrat Ullah, Mariam Anees, Chiea Chuen Khor, Jia Nee Foo, Jia Nee Foo, Outi Makitie, Outi Makitie, Saima Siddiqi

    Diterbitkan 2019-03-01
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  5. 5
    The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability: An exploratory analysis

    The relation between oxytocin receptor gene polymorphisms, adult attachment and Instagram sociability: An exploratory analysis oleh Alessandro Carollo, Andrea Bonassi, Ilaria Cataldo, Giulio Gabrieli, Moses Tandiono, Jia Nee Foo, Bruno Lepri, Gianluca Esposito

    Diterbitkan 2021-09-01
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  6. 6
    High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystrophy

    High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystr... oleh Zhiyong Chen, Yi Jayne Tan, Michelle M. Lian, Moses Tandiono, Jia Nee Foo, Jia Nee Foo, Weng Khong Lim, Weng Khong Lim, Nagaendran Kandiah, Nagaendran Kandiah, Eng-King Tan, Eng-King Tan, Adeline S. L. Ng, Adeline S. L. Ng

    Diterbitkan 2021-02-01
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  7. 7
    Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

    Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta oleh Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo, Mariam Anees

    Diterbitkan 2018-11-01
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  8. 8
    Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

    Correction to: Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta oleh Mehran Kausar, Saima Siddiqi, Muhammad Yaqoob, Sajid Mansoor, Outi Makitie, Asif Mir, Chiea Chuen Khor, Jia Nee Foo, Mariam Anees

    Diterbitkan 2019-04-01
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  9. 9
    Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family

    Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family oleh Muhammad Ajmal, Asif Mir, Sughra Wahid, Chiea Chuen Khor, Jia Nee Foo, Saima Siddiqi, Mehran Kauser, Salman Akbar Malik, Muhammad Nasir

    Diterbitkan 2017-12-01
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  10. 10
    Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis

    Novel Optineurin Frameshift Insertion in a Family With Frontotemporal Dementia and Parkinsonism Without Amyotrophic Lateral Sclerosis oleh Jacqueline Dominguez, Jeryl Tan Yu, Yi Jayne Tan, Arlene Ng, Ma Fe De Guzman, Boots Natividad, Ma Luisa Daroy, Jemellee Cano, Justine Yu, Michelle M. Lian, Li Zeng, Li Zeng, Weng Khong Lim, Weng Khong Lim, Jia Nee Foo, Jia Nee Foo, Adeline S. L. Ng, Adeline S. L. Ng

    Diterbitkan 2021-05-01
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  11. 11
    Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease

    Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease oleh Ethiraj Ravindran, Ethiraj Ravindran, Ethiraj Ravindran, Noor Ullah, Noor Ullah, Shyamala Mani, Shyamala Mani, Shyamala Mani, Elaine Guo Yan Chew, Elaine Guo Yan Chew, Moses Tandiono, Moses Tandiono, Jia Nee Foo, Jia Nee Foo, Chiea Chuen Khor, Chiea Chuen Khor, Angela M. Kaindl, Angela M. Kaindl, Angela M. Kaindl, Saima Siddiqi

    Diterbitkan 2022-10-01
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  12. 12
    A comprehensive association analysis of homocysteine metabolic pathway genes in Singaporean Chinese with ischemic stroke.

    A comprehensive association analysis of homocysteine metabolic pathway genes in Singaporean Chinese with ischemic stroke. oleh Hui-Qi Low, Christopher P L H Chen, Katherine Kasiman, Anbupalam Thalamuthu, Seok-Shin Ng, Jia-Nee Foo, Hui-Meng Chang, Meng-Cheong Wong, E-Shyong Tai, Jianjun Liu

    Diterbitkan 2011-01-01
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  13. 13
    A 3D Fiber‐Hydrogel Based Non‐Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury

    A 3D Fiber‐Hydrogel Based Non‐Viral Gene Delivery Platform Reveals that microRNAs Promote Axon Regeneration and Enhance Functional Recovery Following Spinal Cord Injury oleh Na Zhang, Junquan Lin, Vincent Po Hen Lin, Ulla Milbreta, Jiah Shin Chin, Elaine Guo Yan Chew, Michelle Mulan Lian, Jia Nee Foo, Kunyu Zhang, Wutian Wu, Sing Yian Chew

    Diterbitkan 2021-08-01
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  14. 14
    A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias.

    A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. oleh Saima Siddiqi, Jia Nee Foo, Anthony Vu, Saad Azim, David L Silver, Atika Mansoor, Stacey Kiat Hong Tay, Sumiya Abbasi, Asraf Hussain Hashmi, Jamal Janjua, Sumbal Khalid, E Shyong Tai, Gene W Yeo, Chiea Chuen Khor

    Diterbitkan 2014-01-01
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  15. 15
    C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort

    C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort oleh Yi Jayne Tan, Alisa C. W. Yong, Jia Nee Foo, Michelle M. Lian, Weng Khong Lim, Jacqueline Dominguez, Zhi Hui Fong, Kaavya Narasimhalu, Hui Jin Chiew, Kok Pin Ng, Simon K. S. Ting, Nagaendran Kandiah, Adeline S. L. Ng

    Diterbitkan 2023-04-01
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  16. 16
    Targeted next-generation sequencing to diagnose disorders of HDL cholesterol

    Targeted next-generation sequencing to diagnose disorders of HDL cholesterol oleh Singh N. Sadananda, Jia Nee Foo, Meng Tiak Toh, Lubomira Cermakova, Laia Trigueros-Motos, Teddy Chan, Herty Liany, Jennifer A. Collins, Sima Gerami, Roshni R. Singaraja, Michael R. Hayden, Gordon A. Francis, Jiri Frohlich, Chiea Chuen Khor, Liam R. Brunham

    Diterbitkan 2015-10-01
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  17. 17
    Genetic variants in ER cofactor genes and endometrial cancer risk.

    Genetic variants in ER cofactor genes and endometrial cancer risk. oleh Yuqing Li, Hui-Qi Low, Jia Nee Foo, Hatef Darabi, Kristjana Einarsdόttir, Keith Humphreys, Amanda Spurdle, ANECS Group, Douglas F Easton, Deborah J Thompson, Alison M Dunning, Paul D P Pharoah, Kamila Czene, Kee Seng Chia, Per Hall, Jianjun Liu

    Diterbitkan 2012-01-01
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  18. 18
    Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds

    Biallelic variants in CHST3 cause Spondyloepiphyseal dysplasia with joint dislocations in three Pakistani kindreds oleh Mehran Kausar, Noor Ul Ain, Farzana Hayat, Hunain Fatima, Saad Azim, Hazrat Ullah, Murva Mushtaq, Sumbal Khalid, Shahid Hussain, Sadaf Naz, Jamal Janjua, Saad Bin Amjad, Ruqia Mehmood Baig, Outi Makitie, Raheel Qamar, Shiro Ikegawa, Nishimura Gen, Chiea Chuen Khor, Jia Nee Foo, Saima Siddiqi

    Diterbitkan 2022-08-01
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  19. 19
    Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing.

    Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing. oleh Lai-Ping Wong, Jason Kuan-Han Lai, Woei-Yuh Saw, Rick Twee-Hee Ong, Anthony Youzhi Cheng, Nisha Esakimuthu Pillai, Xuanyao Liu, Wenting Xu, Peng Chen, Jia-Nee Foo, Linda Wei-Lin Tan, Seok-Hwee Koo, Richie Soong, Markus Rene Wenk, Wei-Yen Lim, Chiea-Chuen Khor, Peter Little, Kee-Seng Chia, Yik-Ying Teo

    Diterbitkan 2014-05-01
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  20. 20
    Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells

    Systematic evaluation of CRISPR-Cas systems reveals design principles for genome editing in human cells oleh Yuanming Wang, Kaiwen Ivy Liu, Norfala-Aliah Binte Sutrisnoh, Harini Srinivasan, Junyi Zhang, Jia Li, Fan Zhang, Charles Richard John Lalith, Heyun Xing, Raghuvaran Shanmugam, Jia Nee Foo, Hwee Ting Yeo, Kean Hean Ooi, Tore Bleckwehl, Yi Yun Rachel Par, Shi Mun Lee, Nur Nadiah Binte Ismail, Nur Aidah Binti Sanwari, Si Ting Vanessa Lee, Jan Lew, Meng How Tan

    Diterbitkan 2018-05-01
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