Centre for DNA Fingerprinting and Diagnostics View Homepage


Ontology type: grid:Facility  | foaf:Organization     


Organization Info

NAME

Centre for DNA Fingerprinting and Diagnostics

HOMEPAGE

http://www.cdfd.org.in/

ADDRESS

http://www.grid.ac/institutes/grid.145749.a/address-0

Publications in SciGraph latest 20 shown

  • 2019-12 Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation in BMC MEDICAL GENETICS
  • 2019-04 Spectrum of ARSA variations in Asian Indian patients with Arylsulfatase A deficient metachromatic leukodystrophy in JOURNAL OF HUMAN GENETICS
  • 2019-03 Alström Syndrome Presenting as Isolated Dilated Cardiomyopathy in THE INDIAN JOURNAL OF PEDIATRICS
  • 2019-03 Hydrogen bond-linked pathways of peptide units and polar groups of amino acid residues suitable for electron transfer in cytochrome c proteins in MOLECULAR AND CELLULAR BIOCHEMISTRY
  • 2019-02 Homozygous PCDH12 variants result in phenotype of cerebellar ataxia, dystonia, retinopathy, and dysmorphism in JOURNAL OF HUMAN GENETICS
  • 2018-12 Fission Yeast Sirtuin Hst4 Functions in Preserving Genomic Integrity by Regulating Replisome Component Mcl1 in SCIENTIFIC REPORTS
  • 2018-12 A cross-eyed geneticist’s view II. Riddles, wrapped in mysteries, inside … mealybugs in JOURNAL OF BIOSCIENCES
  • 2018-12 A comprehensive portrait of Y-STR diversity of Indian populations and comparison with 129 worldwide populations in SCIENTIFIC REPORTS
  • 2018-08 Novel splice-site variant of UCHL1 in an Indian family with autosomal recessive spastic paraplegia-79 in JOURNAL OF HUMAN GENETICS
  • 2018-06 Genetic relatedness does not predict the queen’s successors in the primitively eusocial wasp, Ropalidia marginata in JOURNAL OF GENETICS
  • 2018-06 A cross-eyed geneticist’s view in JOURNAL OF BIOSCIENCES
  • 2018-02 Diagnosis and Management of Gaucher Disease in India – Consensus Guidelines of the Gaucher Disease Task Force of the Society for Indian Academy of Medical Genetics and the Indian Academy of Pediatrics in INDIAN PEDIATRICS
  • 2018-02 Ca2+/nuclear factor of activated T cells signaling is enriched in early-onset rectal tumors devoid of canonical Wnt activation in JOURNAL OF MOLECULAR MEDICINE
  • 2018-01 Homozygosity for a nonsense variant in AIMP2 is associated with a progressive neurodevelopmental disorder with microcephaly, seizures, and spastic quadriparesis in JOURNAL OF HUMAN GENETICS
  • 2017-12 Multiple oncogenic roles of nuclear β-catenin in JOURNAL OF BIOSCIENCES
  • 2017-12 Look Up to Diagnose Down! in THE INDIAN JOURNAL OF PEDIATRICS
  • 2017-12 The PPE2 protein of Mycobacterium tuberculosis translocates to host nucleus and inhibits nitric oxide production in SCIENTIFIC REPORTS
  • 2017-11 Genomic adaptation to polyphagy and insecticides in a major East Asian noctuid pest in NATURE ECOLOGY & EVOLUTION
  • 2017-10 Investigation of urinary volatomic alterations in head and neck cancer: a non-invasive approach towards diagnosis and prognosis in METABOLOMICS
  • 2017-08 Variable expressivity and response to bisphosphonate therapy in a family with osteoporosis pseudoglioma syndrome in INDIAN PEDIATRICS
  • JSON-LD is the canonical representation for SciGraph data.

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