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Pallavi Shukla
Pallavi Shukla
ICMR-NIRRCH
Verified email at nirrh.res.in
Title
Cited by
Cited by
Year
Mitochondria in ovarian aging and reproductive longevity
JL Chiang, P Shukla, K Pagidas, NS Ahmed, S Karri, DD Gunn, WW Hurd, ...
Ageing research reviews 63, 101168, 2020
1112020
Mitochondrial dysfunction: An emerging link in the pathophysiology of polycystic ovary syndrome
P Shukla, S Mukherjee
Mitochondrion 52, 24-39, 2020
582020
DNA interstrand cross‐link repair: understanding role of F anconi anemia pathway and therapeutic implications
P Shukla, A Solanki, K Ghosh, BR Vundinti
European journal of haematology 91 (5), 381-393, 2013
262013
Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population
P Shukla, S Vasisht, R Srivastava, N Gupta, M Ghosh, M Kumar, ...
Journal of the neurological sciences 301 (1-2), 38-45, 2011
262011
Current and emerging therapeutic strategies for Fanconi anemia
P Shukla, K Ghosh, BR Vundinti
The HUGO journal 6, 1-8, 2012
212012
Identification of variants in mitochondrial D-loop and oriL region and analysis of mitochondrial DNA copy number in women with polycystic ovary syndrome
P Shukla, S Mukherjee, A Patil
DNA and cell biology 39 (8), 1458-1466, 2020
182020
FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients
A Solanki, P Mohanty, P Shukla, A Rao, K Ghosh, BR Vundinti
PLoS One 11 (1), e0147016, 2016
182016
The mitochondrial landscape of ovarian cancer: emerging insights
P Shukla, KK Singh
Carcinogenesis 42 (5), 663-671, 2021
172021
Molecular genetic studies in Indian patients with megalencephalic leukoencephalopathy
P Shukla, N Gupta, M Ghosh, S Vasisht, S Gulati, P Balakrishnan, ...
Pediatric neurology 44 (6), 450-458, 2011
122011
Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature
P Shukla, A Rao, K Ghosh, BR Vundinti
Gene 518 (2), 470-475, 2013
112013
Molecular characterization of variants in mitochondrial DNA encoded genes using next generation sequencing analysis and mitochondrial dysfunction in women with PCOS
P Shukla, S Mukherjee, A Patil, B Joshi
Gene 855, 147126, 2023
72023
ARID2 suppression promotes tumor progression and upregulates cytokeratin 8, 18 and β-4 integrin expression in TP53-mutated tobacco-related oral cancer and …
P Shukla, P Dange, BS Mohanty, N Gadewal, P Chaudhari, R Sarin
Cancer Gene Therapy 29 (12), 1908-1917, 2022
72022
De novo ABCD1 gene mutation in an Indian patient with adrenoleukodystrophy
N Kumar, P Shukla, KK Taneja, V Kalra, SK Bansal
Pediatric neurology 39 (4), 289-292, 2008
72008
Three novel variants in X-linked adrenoleukodystrophy
P Shukla, N Gupta, M Kabra, M Ghosh, R Sharma, AK Gupta, S Gulati, ...
Journal of child neurology 24 (7), 857-860, 2009
62009
Prenatal diagnosis of megalencephalic leukodystrophy
P Shukla, P Balakrishnan, N Agarwal, M Ghosh, M Kabra, R Sharma, ...
Prenatal Diagnosis: Published in Affiliation With the International Society …, 2008
52008
Uncovering mitochondrial determinants of racial disparities in ovarian cancer
P Shukla, KK Singh
Trends in cancer 7 (2), 93-97, 2021
42021
Molecular analysis of ABCD1 gene in Indian patients with X-linked Adrenoleukodystrophy
P Shukla, N Gupta, S Gulati, M Ghosh, S Vasisht, R Sharma, AK Gupta, ...
Clinica Chimica Acta 412 (23-24), 2289-2295, 2011
42011
Megalencephalic leukodystrophy with simple hemihyperplasia: a rare association
P Shukla, N Gupta, P Balakrishnan, M Ghosh, AK Gupta, R Sharma, ...
Clinical Dysmorphology 18 (1), 49-51, 2009
22009
Mitochondrial epigenetic modifications and nuclear-mitochondrial communication: A new dimension towards understanding and attenuating the pathogenesis in women with PCOS
P Shukla, GC Melkani
Reviews in Endocrine and Metabolic Disorders 24 (2), 317-326, 2023
12023
Prevalence and association of dermatological manifestations with fanconi anemia: A retrospective study
P Shukla, S Korgaonkar, L Kerketta, BR Vundinti
Indian dermatology online journal 9 (5), 341-342, 2018
12018
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Articles 1–20