Mannan, Ashraf U : rechercher sur Z-Library

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1

Genotype-Phenotype Analysis in an Indian Family Affected with Li-Fraumeni Syndrome-Role of Genetic Counselling

Chatterjee, Manjima, Chinder, Pramod, Mannan, Ashraf U., Sheela, M.L., Mukherjee, Upasana, Choudhury, Sheuli, Lo, Caroline, Singh, Suhasini, Singh, Jaya, Hazarika, Diganta, Prabhudesai, Shilpa, Gupta,

Journal:

International Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 457 KB

english, 2016

2

Application of image and sound analysis techniques to monitor the condition of cutting tools

M.A. Mannan, Ashraf A. Kassim, Ma Jing

Journal:

Pattern Recognition Letters

Année:

2000

Langue:

english

Fichier:

PDF, 558 KB

english, 2000

3

Mild Overexpression of Mecp2 in Mice Causes a Higher Susceptibility toward Seizures

Bodda, Chiranjeevi, Tantra, Martesa, Mollajew, Rustam, Arunachalam, Jayamuruga P., Laccone, Franco A., Can, Karolina, Rosenberger, Albert, Mironov, Sergej L., Ehrenreich, Hannelore, Mannan, Ashraf U.

Journal:

The American Journal of Pathology

Année:

2013

Langue:

english

Fichier:

PDF, 2.30 MB

english, 2013

4

Review in formulating the standard form of contract for Industrialized Building System (IBS) construction approach in Malaysia

Mohd Fateh, Mohd Ashraf, Mohammad, Mohammad Fadhil, Abd Shukor, Ani Saifuza, Hasan, A., Khan, A.A., Mannan, Md. A., Hipolito, C.N., Mohamed Sutan, N., Othman, Al-K. Hj., Kabit, M.R., Abdul Wahab, N.

Journal:

MATEC Web of Conferences

Année:

2017

Langue:

english

Fichier:

PDF, 122 KB

english, 2017

5

Mutation Spectrum of GNE Myopathy in the Indian Sub-Continent

Bhattacharya, Sudha, Khadilkar, Satish V., Nalini, Atchayaram, Ganapathy, Aparna, Mannan, Ashraf U., Majumder, Partha P., Bhattacharya, Alok

Journal:

Journal of Neuromuscular Diseases

Année:

2018

Langue:

english

Fichier:

PDF, 72 KB

english, 2018

6

Functional evaluation of paraplegin mutations by a yeast complementation assay

Florian Bonn, Krishna Pantakani, Moneef Shoukier, Thomas Langer, Ashraf U. Mannan

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 272 KB

english, 2010

7

Machine tool condition monitoring using workpiece surface texture analysis

Ashraf A. Kassim, M.A. Mannan, Ma Jing

Journal:

Machine Vision and Applications

Année:

2000

Langue:

english

Fichier:

PDF, 540 KB

english, 2000

8

Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse

Ashraf U. Mannan, Elena Roussa, Cornelia Kraus, Micheal Rickmann, Joerg Maenner, Karim Nayernia, Kerstin Krieglstein, André Reis, Wolfgang Engel

Journal:

Année:

2004

Langue:

english

Fichier:

PDF, 659 KB

english, 2004

9

Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein

Ashraf U. Mannan, Johann Boehm, Simone M. Sauter, Anne Rauber, Paula C. Byrne, Juergen Neesen, Wolfgang Engel

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 339 KB

english, 2006

10

Spastin oligomerizes into a hexamer and the mutant spastin (E442Q) redistribute the wild-type spastin into filamentous microtubule

D. V. Krishna Pantakani, Lakshmipuram S. Swapna, Narayanaswamy Srinivasan, Ashraf U. Mannan

Journal:

Journal of Neurochemistry

Année:

2008

Langue:

english

Fichier:

PDF, 931 KB

english, 2008

11

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia

Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U

Journal:

European Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 162 KB

english, 2008

12

Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia

Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U

Journal:

European Journal of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 43 KB

english, 2009

13

Calgizarrin like gene (Cal) deficient mice undergo normal spermatogenesis

Ashraf U. Mannan, Gabriela Nica, Karim Nayernia, Christian Mueller, Wolfgang Engel

Journal:

Molecular Reproduction and Development

Année:

2003

Langue:

english

Fichier:

PDF, 230 KB

english, 2003

14

Response to Martignoni et al.

Ashraf U. Mannan

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 277 KB

english, 2008

15

Factors affecting recruitment and retention of community health workers in a newborn care intervention in Bangladesh

Syed Moshfiqur Rahman, Nabeel Ashraf Ali, Larissa Jennings, M Habibur R Seraji, Ishtiaq Mannan, Rasheduzzaman Shah, Arif Billah Al-Mahmud, Sanwarul Bari, Daniel Hossain, Milan Krishna Das, Abdullah H

Journal:

Human Resources for Health

Année:

2010

Langue:

english

Fichier:

PDF, 640 KB

english, 2010

16

ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia

Ashraf U. Mannan, Philip Krawen, Simone M. Sauter, Johann Boehm, Agnieszka Chronowska, Walter Paulus, Juergen Neesen, Wolfgang Engel

Journal:

The American Journal of Human Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 360 KB

english, 2006

17

Sall1, Sall2, and Sall4 Are Required for Neural Tube Closure in Mice

Johann Böhm, Anja Buck, Wiktor Borozdin, Ashraf U. Mannan, Uta Matysiak-Scholze, Ibrahim Adham, Walter Schulz-Schaeffer, Thomas Floss, Wolfgang Wurst, Jürgen Kohlhase, Francisco Barrionuevo

Journal:

The American Journal of Pathology

Année:

2008

Langue:

english

Fichier:

PDF, 1.48 MB

english, 2008

18

Investigation of in vivo neuropharmacological effect of Alpinia nigra leaf extract

Sharmen, Farjana, Mannan, Adnan, Rahman, Md. Mominur, Chowdhury, Md. Ashraf Uddin, Uddin, Muhammad Erfan, Ahmed, A.M. Abu

Journal:

Asian Pacific Journal of Tropical Biomedicine

Année:

2014

Langue:

english

Fichier:

PDF, 474 KB

english, 2014

19

Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India

Mannan, Ashraf U, Singh, Jaya, Lakshmikeshava, Ravikiran, Thota, Nishita, Singh, Suhasini, Sowmya, T S, Mishra, Avshesh, Sinha, Aditi, Deshwal, Shivani, Soni, Megha R, Chandrasekar, Anbukayalvizhi, Ra

Journal:

Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 589 KB

english, 2016

20

Prominent Eustachian Valve in Newborns: A Report of Four Cases

Gad, Ashraf, Mannan, Javed, Chhabra, Manoj, Zhang, Xi, Narula, Pramod, Hoang, Danthanh

Journal:

American Journal of Perinatology Reports

Année:

2015

Langue:

english

Fichier:

PDF, 261 KB

english, 2015

21

Homozygosity mapping guided next generation sequencing to identify the causative genetic variation in inherited retinal degenerative diseases

Sundaramurthy, Srilekha, Swaminathan, Meenakshi, Sen, Parveen, Arokiasamy, Tharigopala, Deshpande, Swati, John, Neetha, Gadkari, Rupali A, Mannan, Ashraf U, Soumittra, Nagasamy

Journal:

Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 1.12 MB

english, 2016

22

Clinical and genetic analysis of Indian patients with NDP-related retinopathies

Sudha, Dhandayuthapani, Ganapathy, Aparna, Mohan, Puja, Mannan, Ashraf U., Krishna, Shuba, Neriyanuri, Srividya, Swaminathan, Meenakshi, Rishi, Pukhraj, Chidambaram, Subbulakshmi, Arunachalam, Jayamur

Journal:

International Ophthalmology

Année:

2017

Langue:

english

Fichier:

PDF, 1.07 MB

english, 2017

23

Incidental Findings in Male Breast Carcinoma: A Genetic Counseling Approach

Chatterjee, Manjima, Sheela, M.L., Mukherjee, Upasana, Patil, Shekar, Satheesh, C.T., Murugan, Krithika, Naik, Radheshyam, Rao, Nalini, Mahesh, B., Mannan, U. Ashraf, Gupta, Vaijayanti, Sankaran, Sati

Journal:

International Journal of Human Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 274 KB

english, 2016

24

Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia

Rangaraju, Advithi, Krishnan, Shuba, Aparna, G., Sankaran, Satish, Mannan, Ashraf U., Rao, B. Hygriv

Journal:

Indian Pacing and Electrophysiology Journal

Année:

2018

Langue:

english

Fichier:

PDF, 189 KB

english, 2018

25

Oligomerization of ZFYVE27 (Protrudin) Is Necessary to Promote Neurite Extension

Pantakani, D. V. Krishna, Czyzewska, Marta M., Sikorska, Anna, Bodda, Chiranjeevi, Mannan, Ashraf U., Gasset, Maria

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 1.23 MB

english, 2011

26

Purkinje Cell Compartmentation in the Cerebellum of the Lysosomal Acid Phosphatase 2 Mutant Mouse (Nax - Naked-Ataxia Mutant Mouse)

Bailey, Karen, Rahimi Balaei, Maryam, Mannan, Ashraf, Del Bigio, Marc R., Marzban, Hassan, Sugihara, Izumi

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 7.05 MB

english, 2014

27

Chronic Mucocutaneous Candidiasis in an Adolescent Boy Due to a Novel Mutation in TRAF3IP2

Bhattad, Sagar, Dinakar, Chitra, Pinnamaraju, Haneesha, Ganapathy, Aparna, Mannan, Ashraf

Journal:

Journal of Clinical Immunology

Année:

2019

Langue:

english

Fichier:

PDF, 596 KB

english, 2019

28

Homozygous sequestosome 1 ( SQSTM1 ) mutation: a rare cause for childhood-onset progressive cerebellar ataxia with vertical gaze palsy

Vedartham, Veena, Sundaram, Soumya, Nair, Sruthi S, Ganapathy, Aparna, Mannan, Ashraf, Menon, Ramshekhar

Journal:

Ophthalmic Genetics

Année:

2019

Langue:

english

Fichier:

PDF, 1.02 MB

english, 2019

29

Bacterial Isolates of Early Onset Neonatal Sepsis and Their Antibiotic Susceptibility Pattern

Mannan, Md Abdul, Iqbal, Shahed, Karim, SM Rezaul, Ahmed, Talim Uddin, Khan, Md Hakimul Haque, Ahmed, Ashraf Uddin, Dey, Subir, Yasmin, Sabina, Ferdous, Navila

Journal:

Chattagram Maa-O-Shishu Hospital Medical College Journal

Année:

2018

Langue:

english

Fichier:

PDF, 1.49 MB

english, 2018

30

Lipoprotein Lipase Deficiency

Kuthiroly, Shwetha, Yesodharan, Dhanya, Radhakrishnan, Natasha, Ganapathy, Aparna, Mannan, Ashraf U, Hoffmann, Michael M., Nampoothiri, Sheela

Journal:

Indian Journal of Pediatrics

Année:

2020

Fichier:

PDF, 752 KB

2020

31

Genotype-phenotype correlates of infantile-onset developmental & epileptic encephalopathy syndromes in South India: a single centre experience

Mitta, Nandini, Menon, Ramshekhar N, McTague, Amy, Radhakrishnan, Ashalatha, Sundaram, Soumya, Cherian, Ajith, Madhavilatha, GK, Mannan, Ashraf U, Nampoothiri, Sheela, Thomas, Sanjeev V

Journal:

Epilepsy Research

Année:

2020

Fichier:

PDF, 2.07 MB

2020

32

Lethal Cenani Lenz syndrome in two consecutive pregnancies: Further extension of phenotype from Maldives

Yesodharan, Dhanya, Krishnan, Vivek, Nair, Indu R., Ganapathy, Aparna, Mannan, Ashraf U., Nampoothiri, Sheela

Journal:

American Journal of Medical Genetics Part A

Année:

2020

Fichier:

PDF, 2.31 MB

2020