Publications by authors named "Bakshi D"

Article Synopsis
  • Atopic dermatitis (AD) is a chronic skin condition that can severely affect patients' quality of life, including their sexual well-being.
  • A study assessed the impact of moderate-to-severe AD on sexual health and the effectiveness of two treatments, abrocitinib and dupilumab, over a year.
  • Results showed that before treatment, a large majority of patients felt their condition affected their sex life negatively, but after 52 weeks of therapy, these negative feelings and behaviors significantly decreased.
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Background: Serum-sickness like reactions (SSLRs) to amoxicillin have been documented in the medical literature. Beta-lactams are important and commonly used medications especially in the pediatric population. Often, SSLRs present within days of and during first exposure/ingestion to the offending agent.

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  • Ovarian and breast cancers are common in Jammu and Kashmir, but studies on their genetic associations, particularly the TP63 gene variant rs10937405, are scarce in this region.
  • A study involving 150 breast cancer cases, 150 ovarian cancer cases, and 210 healthy controls was conducted to evaluate the association of this gene variant using genetic testing methods.
  • Results showed no significant risk associated with the variant for either cancer type, suggesting that further research with a larger sample size is necessary to explore other variants of the TP63 gene.
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Multiple myeloma (MM), the second most common hematological malignancy, is generally considered incurable because of the development of drug resistance. We previously reported that hyaluronan and proteoglycan link protein 1 (HAPLN1) produced by stromal cells induces activation of NF-κB, a tumor-supportive transcription factor, and promotes drug resistance in MM cells. However, the identity of the cell surface receptor that detects HAPLN1 and thereby engenders pro-tumorigenic signaling in MM cells remains unknown.

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Objectives: To assess the difficulties faced by the pregnant women in seeking appropriate antenatal care due to the restrictions imposed during the COVID-19 pandemic; assess the difficulties encountered during delivery and postpartum period; the suitability of the teleconsultation services offered; effect of COVID-19 infection on pregnancy outcomes and the effect of restrictions on the nutrition profile of the pregnant women.

Design: Prospective observational study.

Setting And Participants: We included 1374 pregnant women from the rural areas of three districts of Punjab, India registered at government health centres before the implementation of lockdown due to the COVID-19 pandemic on 24 March 2020.

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  • The study examines the genetic variant rs10937405 and its association with leukemia specifically in the North Indian population of Jammu and Kashmir, which has not been previously explored.
  • The research involved 588 individuals (188 with leukemia and 400 controls), and used a TaqMan assay to analyze the genetic variant.
  • Results showed a significant association between rs10937405 and leukemia, indicating it may serve as a risk factor, potentially aiding in the development of diagnostic markers for leukemia in this population.
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  • * Previous research has identified a connection between certain genetic variations (SNPs) in the ARID5B gene and increased CRC risk, yet the status of this association in north Indian populations remains unclear.
  • * This study found that the SNP variant rs10740055 in the ARID5B gene significantly increases CRC risk, with a reported odds ratio of 3.35, suggesting that individuals carrying the A allele are at a higher risk; larger studies are recommended for further confirmation.
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  • * The study found significant associations between five specific SNPs and CRC, with odds ratios indicating increased risk for these genetic variants among cases compared to controls.
  • * This research is the first of its kind in the J&K population to connect these genetic variants to colorectal cancer, suggesting further studies in diverse populations could enhance understanding of genetic risks in CRC.
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  • Lung cancer is a varied disease, with non-small cell lung cancer (NSCLC) making up 80% of cases and small cell lung cancer (SCLC) 20%.
  • A study was conducted using a high-throughput genotyping method to analyze genetic variants in 723 samples, including 162 NSCLC patients and 592 healthy controls.
  • Six specific genetic variants were found to significantly relate to NSCLC risk in the Jammu and Kashmir population, showing promise for further research to uncover the genetic factors linked to this type of lung cancer.
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Introduction: The reported use of cannabis within surgical population is increasing. Cannabis use is potentially associated with increased harms and varied effects on pain control. These have important implications to perioperative care.

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Leukemia is a heterogeneous disorder, characterized by elevated proliferation of white blood cells. In this study, we explored the association of 17 genetic variants with leukemia patients in the Jammu and Kashmir region of north India. The variants were genotyped by using a high-throughput Agena MassARRAY platform in 758 individuals (166 cases and 592 controls).

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Aim: In this study, we evaluated the association of rs6964823 of the Ikaros Family Zinc Finger 1 (IKZF1) gene with the risk of colorectal cancer (CRC) within the population of Jammu and Kashmir (J and K).

Materials And Methods: The variant rs6964823 of the IKZF1 gene was genotyped using the TaqMan allele discrimination assay for 578 individuals (182 CRC cases and 396 healthy controls). The association of single-nucleotide polymorphisms with the disease was evaluated using logistic regression.

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Breast cancer has replaced cervical cancer as being the most common and having the highest mortality among women in India. gene is conserved among organisms during evolutionary succession and is a member of LEM family proteins in lower metazoans and is involved in critical functions in the nuclear architecture, gene expression and cell signaling. is the human orthologous of LEM-3 and is involved in DNA damage response and DNA repair.

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Ovarian cancer (OC), a multifaceted and genetically heterogeneous malignancy is one of the most common cancers among women. The aim of the study is to unravel the genetic factors associated with OC and the extent of genetic heterogeneity in the populations of Jammu and Kashmir (J&K).Using the high throughput Agena MassARRAY platform, present case control study was designed which comprises 200 histopathological confirmed OC patients and 400 age and ethnicity matched healthy controls to ascertain the association of previously reported eleven single nucleotide polymorphisms (SNPs) spread over ten genes (DNMT3A, PIK3CA, FGFR2, GSTP1, ERCC5, AKT1, CASC16, CYP19A1, BCL2 and ERCC1) within the OC population of Jammu and Kashmir, India.

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Background And Aim: There is sparse data available on human subjects regarding the affect of excessive fluoride exposures on pregnancy. The aim of this study was to examine the association between elevated urinary fluoride levels during early pregnancy and maternal anemia and adverse fetal outcome.

Patients And Methods: We enrolled 600 pregnant patients with gestational age less than 20 weeks and with a high urinary fluoride levels(>1 mg/L).

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Background: Breast Cancer (BC) is associated with inherited gene mutations. High throughput genotyping of BC samples has led to the identification and characterization of biomarkers for the diagnosis of BC. The most common genetic variants studied are SNPs (Single Nucleotide Polymorphisms) that determine susceptibility to an array of diseases thus serving as a potential tool for identifying the underlying causes of breast carcinogenesis.

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Background: MassARRAY (Agena Bioscience™) combines competitive PCR with MALDI-TOF mass spectrometry (MS) analysis that gives highly accurate, sensitive, and high-throughput methods for the quantitative analysis of variation of gene expression in multiple samples. SNPs (Single Nucleotide Polymorphisms) have a very high potential of discovering disease-gene relationships. SNP-genotyping through MassARRAY is not only a cost-effective genotyping method but also provides a platform to validate variants observed through a high-throughput Next-generation sequencing (NGS).

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Background: 8-Oxo-7, 8-dihydro-2'-deoxyguanosine (8-oxodG) is a potent DNA damage marker that leads to cellular oxidative stress. It is a DNA-repair enzyme that participates in "8-oxodG" DNA adducts removal. Previous studies show weak associations of rs1052133 (hOGG1) in breast cancer patients of Northern India.

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In the published article [1] the statement under the subheading 'Consent for publication' is incorrect.

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Objective: To investigate the association of newly identified genetic variants G>A (rs2285947) of the DNAH11 gene and G>A (rs2494938) of the LRFN2 gene with ovarian and breast cancers in women belonging to Jammu and Kashmir state, where the prevalence of ovarian and breast cancers is remarkably high in the population.

Methods: A candidate gene prospective case-control association study design was adopted, in which 354 cases (219 cases of ovarian cancer and 135 cases of breast cancer) were histopathologically confirmed and 330 healthy controls matched for age and ethnicity were recruited. The details of cases and controls were also recorded in a predesigned pro forma after their written informed consent.

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This retrospective case series details a single-center experience of 8 patients (mean age, 54.4 years) with celiac artery aneurysms (CAAs) who underwent 1 parent vessel-sparing, 5 partial parent vessel-sparing, and 2 non-parent vessel-sparing procedures. Technical success was achieved in 6 of 8 (75%) patients.

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