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Mukhtar Ullah

Showing results (11-20 of 32) with videos related to

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Annals of Medicine|March 3, 2025
Exome sequencing identifies a homozygous splice site variant in <i>RP1</i> as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani familyAbdur Rashid, Asad Munir, Muhammad Zahid, et al.
Diagnostics (Basel, Switzerland)|November 11, 2022
A Hybrid Preprocessor DE-ABC for Efficient Skin-Lesion Segmentation with Improved ContrastShairyar Malik, Tallha Akram, Imran Ashraf, et al.
Journal of Theoretical Biology|December 17, 2016
On p53 revival using system oriented drug dosage designMuhammad Haseeb, Shumaila Azam, A I Bhatti, et al.
BMC Ophthalmology|March 24, 2023
A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani familyNobia Aziz, Mukhtar Ullah, Abdur Rashid, et al.
Ophthalmic Research|April 24, 2023
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA SplicingMukhtar Ullah, Atta Ur Rehman, Marc Folcher, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|April 29, 2019
Wnt Signaling: A Potential Therapeutic Target in Head and Neck Squamous Cell CarcinomaZeeshan Javed, Hafiz Muhammad Farooq, Mukhtar Ullah, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
BMC Ophthalmology|May 10, 2023
Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous familiesMuhammad Marwan, Muhammad Dawood, Mukhtar Ullah, et al.
Human Genome Variation|April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Annals of Medicine|March 3, 2025
Exome sequencing identifies a homozygous splice site variant in <i>RP1</i> as the underlying cause of autosomal recessive retinitis pigmentosa in a Pakistani familyAbdur Rashid, Asad Munir, Muhammad Zahid, et al.
Diagnostics (Basel, Switzerland)|November 11, 2022
A Hybrid Preprocessor DE-ABC for Efficient Skin-Lesion Segmentation with Improved ContrastShairyar Malik, Tallha Akram, Imran Ashraf, et al.
Journal of Theoretical Biology|December 17, 2016
On p53 revival using system oriented drug dosage designMuhammad Haseeb, Shumaila Azam, A I Bhatti, et al.
BMC Ophthalmology|March 24, 2023
A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani familyNobia Aziz, Mukhtar Ullah, Abdur Rashid, et al.
Ophthalmic Research|April 24, 2023
A Novel Intronic Deletion in PDE6B Causes Autosomal Recessive Retinitis Pigmentosa by Interfering with RNA SplicingMukhtar Ullah, Atta Ur Rehman, Marc Folcher, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|April 29, 2019
Wnt Signaling: A Potential Therapeutic Target in Head and Neck Squamous Cell CarcinomaZeeshan Javed, Hafiz Muhammad Farooq, Mukhtar Ullah, et al.
Ophthalmic Genetics|November 21, 2024
A novel homozygous missense variant in <i>POC1B</i> causes cone dystrophy in a consanguineous Pakistani familyAsad Munir, Inam Ullah Khan, Abdur Rashid, et al.
BMC Ophthalmology|May 10, 2023
Unravelling the genetic basis of retinal dystrophies in Pakistani consanguineous familiesMuhammad Marwan, Muhammad Dawood, Mukhtar Ullah, et al.
Human Genome Variation|April 27, 2026
Duplication of 4-bp in SACS leads to autosomal recessive spastic ataxia of Charlevoix-Saguenay type in two Pakistani patientsSaba Bibi, Asad Munir, Fawad Ali, et al.
Human Genome Variation|November 18, 2025
A novel homozygous DST variant causes hereditary sensory and autonomic neuropathy in a Pakistani familyAsad Munir, Helen Nabiryo Frederiksen, Fawad Ali, et al.
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