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Sadaf Naz

Showing results (41-50 of 89) with videos related to

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Journal of Medical Genetics|May 6, 2015
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing lossGhulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, et al.
Biochemical and Biophysical Research Communications|September 19, 2024
Protective potential of Bacillus subtilis (NMCC-path-14) against extraarticular manifestations during acute and sub-acute phase of arthritis using mice modelMuhammad Usama Mazhar, Sadaf Naz, Jehan Zeb Khan, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|November 6, 2023
Immunostimulant, hepatoprotective, and nephroprotective potential of Bacillus subtilis (NMCC-path-14) in comparison to dexamethasone in alleviating CFA-induced arthritisMuhammad Usama Mazhar, Sadaf Naz, Tayyaba Zulfiqar, et al.
European Journal of Medical Genetics|October 26, 2018
Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type MaroteauxNoor Ul Ain, Muddassar Iqbal, Helena Valta, et al.
Journal of Medical Genetics|June 28, 2020
Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in <i>GNPNAT1</i>Noor Ul Ain, Marta Baroncelli, Alice Costantini, et al.
Scientific Reports|February 19, 2026
Studies on intellectual disability identify variants in established genes as well as confirm candidature of new genesAmina Iftikhar Butt, Fariya Khan Bazai, Kaleemullah Kakar, et al.
Inflammopharmacology|February 26, 2025
Bacillus subtilis (NMCC-path-14) ameliorates acute phase of arthritis via modulating NF-κB and Nrf-2 signaling in mice modelMuhammad Usama Mazhar, Sadaf Naz, Tayyaba Zulfiqar, et al.
European Journal of Medical Genetics|May 30, 2020
A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous familySamina Yasin, Saima Mustafa, Arzoo Ayesha, et al.
Biological Research|July 24, 2014
Compositional studies and Biological activities of Perovskia abrotanoides Kar. oilsSadaf Naz Ashraf, Muhammad Zubair, Komal Rizwan, et al.
Pageof 9

Showing results (41-50 of 89) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|May 6, 2015
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing lossGhulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, et al.
Biochemical and Biophysical Research Communications|September 19, 2024
Protective potential of Bacillus subtilis (NMCC-path-14) against extraarticular manifestations during acute and sub-acute phase of arthritis using mice modelMuhammad Usama Mazhar, Sadaf Naz, Jehan Zeb Khan, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|November 6, 2023
Immunostimulant, hepatoprotective, and nephroprotective potential of Bacillus subtilis (NMCC-path-14) in comparison to dexamethasone in alleviating CFA-induced arthritisMuhammad Usama Mazhar, Sadaf Naz, Tayyaba Zulfiqar, et al.
European Journal of Medical Genetics|October 26, 2018
Novel variants in natriuretic peptide receptor 2 in unrelated patients with acromesomelic dysplasia type MaroteauxNoor Ul Ain, Muddassar Iqbal, Helena Valta, et al.
Journal of Medical Genetics|June 28, 2020
Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in <i>GNPNAT1</i>Noor Ul Ain, Marta Baroncelli, Alice Costantini, et al.
Scientific Reports|February 19, 2026
Studies on intellectual disability identify variants in established genes as well as confirm candidature of new genesAmina Iftikhar Butt, Fariya Khan Bazai, Kaleemullah Kakar, et al.
Inflammopharmacology|February 26, 2025
Bacillus subtilis (NMCC-path-14) ameliorates acute phase of arthritis via modulating NF-κB and Nrf-2 signaling in mice modelMuhammad Usama Mazhar, Sadaf Naz, Tayyaba Zulfiqar, et al.
European Journal of Medical Genetics|May 30, 2020
A novel homozygous missense variant in MATN3 causes spondylo-epimetaphyseal dysplasia Matrilin 3 type in a consanguineous familySamina Yasin, Saima Mustafa, Arzoo Ayesha, et al.
Biological Research|July 24, 2014
Compositional studies and Biological activities of Perovskia abrotanoides Kar. oilsSadaf Naz Ashraf, Muhammad Zubair, Komal Rizwan, et al.
Pageof 9