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1

Study of the association of forkhead box P3 (FOXP3) gene polymorphisms with unexplained recurrent spontaneous abortions in Indian population

Mishra, Shivani, Srivastava, Anukool, Mandal, Kausik, Phadke, Shubha R.

Journal:

Journal of Genetics

Year:

2018

Language:

english

File:

PDF, 354 KB

english, 2018

2

Effect of behaviour change communication on qualified medical care-seeking for sick neonates among urban poor in Lucknow, northern India: a before and after intervention study

Shally Awasthi, Neeraj M. Srivastava, Girdhar G. Agarwal, Shubha Pant, Tej P. Ahluwalia

Journal:

Tropical Medicine & International Health

Year:

2009

Language:

english

File:

PDF, 286 KB

english, 2009

3

Trichoderma: A scientific approach against soil borne pathogens

Mukesh, Srivastava, Mohammad, Shahid, Sonika, Pandey, Vipul, Kuma, Anuradha, Singh, Shubha, Trived, Srivastava, Y K, Shivram,

Journal:

African Journal of Microbiology Research

Year:

2015

Language:

english

File:

PDF, 479 KB

english, 2015

4

Prevalence, risk factors and virological profile of chronic hepatitis b virus infection in pregnant women in India

Chandana Pande, Shiv Kumar Sarin, Sharda Patra, Kazila Bhutia, Siddhartha Kumar Mishra, Sangeeta Pahuja, Manjula Jain, Shikha Srivastava, Sadaf Bashir Dar, Shubha Sagar Trivedi, Chinmay K. Mukhopadhya

Journal:

Journal of Medical Virology

Year:

2011

Language:

english

File:

PDF, 85 KB

english, 2011

5

Behavioral and neurochemical effects induced by pyrethroid-based mosquito repellent exposure in rat offsprings during prenatal and early postnatal period

Chaitali Sinha, Kavita Seth, Fakhrul Islam, Rajnish Kumar Chaturvedi, Shubha Shukla, Neeraj Mathur, N. Srivastava, Ashok Kumar Agrawal

Journal:

Neurotoxicology and Teratology

Year:

2006

Language:

english

File:

PDF, 386 KB

english, 2006

6

Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population

Pallavi Shukla, Suman Vasisht, Ranjana Srivastava, Neerja Gupta, Manju Ghosh, Manoj Kumar, Raju Sharma, Arun K. Gupta, Punit Kaur, Mahesh Kamate, Sheffali Gulati, Veena Kalra, Shubha Phadke, Pratibha

Journal:

Journal of the Neurological Sciences

Year:

2011

Language:

english

File:

PDF, 663 KB

english, 2011

7

Molecular diversity and phylogeny in geographical collection of chickpea (Cicersp.) accessions

BHARADWAJ, C., SRIVASTAVA, RACHNA, CHAUHAN, S. K., SATYAVATHI, C. TARA, KUMAR, J., FARUQUI, AFZAL, YADAV, SHUBHA, RIZVI, AQEEL HASAN, KUMAR, TAPAN

Journal:

Journal of Genetics

Year:

2013

Language:

english

File:

PDF, 628 KB

english, 2013

8

Mutations in patients with osteogenesis imperfecta from consanguineous Indian families

Stephen, Joshi, Girisha, Katta Mohan, Dalal, Ashwin, Shukla, Anju, Shah, Hitesh, Srivastava, Priyanka, Kornak, Uwe, Phadke, Shubha R.

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 1.53 MB

english, 2015

9

Consanguinity as an Adjunct Diagnostic Tool

Srivastava, Priyanka, Saxena, Deepti, Joshi, Stephen, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 1.20 MB

english, 2016

10

Hunter syndrome in northern India: Clinical features and mutation spectrum

Narayanan, Dhanya Lakshmi, Srivastava, Priyanka, Mandal, Kausik, Gambhir, Poonam Singh, Phadke, Shubha R.

Journal:

Indian Pediatrics

Year:

2016

Language:

english

File:

PDF, 451 KB

english, 2016

11

Cartilage Hair Hypoplasia: Two Unrelated Cases with g.70 A > G Mutation in RMRP Gene

Narayanan, Dhanya Lakshmi, Shukla, Anju, Siddesh, Anju Rani, Stephen, Joshi, Srivastava, Priyanka, Mandal, Kausik, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 338 KB

english, 2016

12

Floating Harbor Syndrome

Amita, Moirangthem, Srivastava, Priyanka, Agarwal, Divya, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2016

Language:

english

File:

PDF, 315 KB

english, 2016

13

Pycnodysostosis

Mandal, Kausik, Ray, Sayantan, Saxena, Deepti, Srivastava, Priyanka, Moirangthem, Amita, Ranganath, Prajnya, Gupta, Neerja, Mukhopadhyay, Satinath, Kabra, Madhulika, Phadke, Shubha R.

Journal:

Clinical Dysmorphology

Year:

2016

Language:

english

File:

PDF, 429 KB

english, 2016

14

Fanconi-Bickel Syndrome: Another Novel Mutation inSLC2A2

Amita, Moirangthem, Srivastava, Priyanka, Mandal, Kausik, De, Sudarsana, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2017

Language:

english

File:

PDF, 503 KB

english, 2017

15

Acetyl-l-Carnitine via Upegulating Dopamine D1 Receptor and Attenuating Microglial Activation Prevents Neuronal Loss and Improves Memory Functions in Parkinsonian Rats

Singh, Sonu, Mishra, Akanksha, Srivastava, Neha, Shukla, Rakesh, Shukla, Shubha

Journal:

Molecular Neurobiology

Year:

2016

Language:

english

File:

PDF, 8.40 MB

english, 2016

16

MK-801 (Dizocilpine) Regulates Multiple Steps of Adult Hippocampal Neurogenesis and Alters Psychological Symptoms via Wnt/β-Catenin Signaling in Parkinsonian Rats

Singh, Sonu, Mishra, Akanksha, Srivastava, Neha, Shukla, Shubha

Journal:

ACS Chemical Neuroscience

Year:

2017

Language:

english

File:

PDF, 6.85 MB

english, 2017

17

Spondyloepiphyseal dysplasia Omani type: CHST3 mutation spectrum and phenotypes in three Indian families

Srivastava, Priyanka, Pandey, Himani, Agarwal, Divya, Mandal, Kausik, Phadke, Shubha R.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 781 KB

english, 2017

18

Novel mutations in the transmembrane natriuretic peptide receptorNPR-Bgene in four Indian families with acromesomelic dysplasia, type Maroteaux

SRIVASTAVA, PRIYANKA, TUTEJA, MONI, DALAL, ASHWIN, MANDAL, KAUSIK, PHADKE, SHUBHA R.

Journal:

Journal of Genetics

Year:

2016

Language:

english

File:

PDF, 4.88 MB

english, 2016

19

Novel sequence variations in the thymidine phosphorylase gene causing mitochondrial neurogastrointestinal encephalopathy

Karyampudi, Arun, Srivastava, Priyanka, Mandal, Kausik, Yadav, Prabhaker, Ghoshal, Uday C., Verma, Abhai, Phadke, Shubha R.

Journal:

Clinical Dysmorphology

Year:

2016

Language:

english

File:

PDF, 445 KB

english, 2016

20

KBG syndrome

Srivastava, Priyanka, Gambhir, Poonam S., Phadke, Shubha R.

Journal:

Clinical Dysmorphology

Year:

2017

Language:

english

File:

PDF, 235 KB

english, 2017

21

Expansion of the phenotypic spectrum in three families of methyl CpG-binding protein 2 duplication syndrome

Moirangthem, Amita, Tuteja Bhatia, Moni, Srivastava, Priyanka, Mandal, Kausik, Rai, Archana, Phadke, Shubha R.

Journal:

Clinical Dysmorphology

Year:

2017

Language:

english

File:

PDF, 245 KB

english, 2017

22

Pyruvate Carboxylase Deficiency Mimicking Diabetic Ketoacidosis

Mangla, Pragya, Gambhir, Poonam Singh, Sudhanshu, Siddhnath, Srivastava, Priyanka, Rai, Archana, Bhatia, Vijayalakshmi, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2017

Language:

english

File:

PDF, 355 KB

english, 2017

23

Large Periapical or Cystic Lesions in Association with Roots Having Open Apices Managed Nonsurgically Using 1-step Apexification Based on Platelet-rich Fibrin Matrix and Biodentine Apical Barrier: A Case Series

Sharma, Sarang, Sharma, Vivek, Passi, Deepak, Srivastava, Dhirendra, Grover, Shibani, Dutta, Shubha Ranjan

Journal:

Journal of Endodontics

Year:

2017

Language:

english

File:

PDF, 1.51 MB

english, 2017

24

Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL)

Mishra, Shivani, Pandey, Himani, Srivastava, Priyanka, Mandal, Kausik, Phadke, Shubha R.

Journal:

Indian Journal of Pediatrics

Year:

2018

Language:

english

File:

PDF, 370 KB

english, 2018

25

Phenotypic characterization of derivative 22 syndrome: case series and review

Saxena, Deepti, Srivastava, Priyanka, Tuteja, Moni, Mandal, Kausik, Phadke, Shubha R

Journal:

Journal of Genetics

Year:

2018

Language:

english

File:

PDF, 2.41 MB

english, 2018

26

Sequence variations in TENM3 gene causing eye anomalies with intellectual disability: Expanding the phenotypic spectrum

Singh, Bharti, Srivastava, Priyanka, Phadke, Shubha R.

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 1.22 MB

english, 2018

27

A large interstitial 11q deletion with isolated mild intellectual disability

Lallar, Meenakshi, Srivastava, Priyanka, Phadke, Shubha R.

Journal:

Clinical Dysmorphology

Year:

2018

Language:

english

File:

PDF, 138 KB

english, 2018

28

Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls

Lallar, Meenakshi, Rai, Archana, Srivastava, Priyanka, Mandal, Kausik, Gupta, Neerja, Kabra, Madhulika, Phadke, Shubha R.

Journal:

Indian Pediatrics

Year:

2018

Language:

english

File:

PDF, 469 KB

english, 2018

29

PIERS calculator- predicting adverse maternal outcome in preeclampsia

Srivastava, Shubha, Parihar, Bharti Chaudhary, Jain, Neha

Journal:

International Journal of Reproduction, Contraception, Obstetrics and Gynecology

Year:

2017

Language:

english

File:

PDF, 628 KB

english, 2017

30

Physiological and biochemical analysis of Trichoderma species isolated from different location U. P.

Anuradha, Singh Sonika Pandey, Mukesh, Srivastava, Mohammad, Shahid, Vipul, Kumar, Shubha, Trivadi, Ved, Ratan

Journal:

African Journal of Agricultural Research

Year:

2015

Language:

english

File:

PDF, 161 KB

english, 2015

31

Deletion 7q21.2-q22.1 in a case with split hand-split foot malformation, sensorineural hearing loss and intellectual disability: Phenotype subtypes and the correlation with genotypes

Rai, Archana, Srivastava, Priyanka, Phadke, Shubha R.

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 1.34 MB

english, 2018

32

Analytical study of adolescent pregnancies at a tertiary care centre

Srivastava, Shubha, Chandra, Madhuri, Singh, Umesh Kumar

Journal:

International Journal of Reproduction, Contraception, Obstetrics and Gynecology

Year:

2017

Language:

english

File:

PDF, 350 KB

english, 2017

33

Cytogenetic microarray in structurally normal and abnormal foetuses: a five years experience elucidating increasing acceptance and clinical utility

Lallar, Meenakshi, Srivastava, Priyanka, Rai, Archana, Saxena, Deepti, Mandal, Kausik, Phadke, Shubha R.

Journal:

Journal of Genetics

Year:

2019

Language:

english

File:

PDF, 549 KB

english, 2019

34

Trichoderma: A magical weapon against soil borne pathogens

Mukesh, Srivastava, Sonika, P, ey,, Mohammad, Shahid, Vipul, Kumar, Anuradha, Singh, Shubha, Trivedi, Yatindra, Kumar Srivastava

Journal:

African Journal of Agricultural Research

Year:

2015

Language:

english

File:

PDF, 414 KB

english, 2015

35

A mild phenotype of LGI4-Related arthrogryposis multiplex congenita with intrafamilial variability

Mishra, Shivani, Rai, Archana, Srivastava, Priyanka, Phadke, Shubha R.

Journal:

European Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 647 KB

english, 2019

36

Hypotonic infant with PallisterâKillian syndrome diagnosed by cytogenetic microarray, without pigmentary skin changes and malformations

Rawool, Anup, Srivastava, Priyanka, Phadke, Shubha R.

Journal:

Journal of Genetics

Year:

2020

File:

PDF, 470 KB

2020

37

Management of Fusarium Wilt using mycolytic enzymes produced by Trichoderma harzianum (Th. Azad)

Mohammad, Shahid, Mukesh, Srivastava, Sonika, Pandey, Vipul, Kumar, Anuradha, Singh, Shubha, Trivedi, Y, K Srivastava, Shiv, Ram

Journal:

AFRICAN JOURNAL OF BIOTECHNOLOGY

Year:

2015

File:

PDF, 534 KB

2015