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Page 1
IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis.
Chekuri A, Guru AA, Biswas P, Branham K, Borooah S, Soto-Hermida A, Hicks M, Khan NW, Matsui H, Alapati A, Raghavendra PB, Roosing S, Sarangapani S, Mathavan S, Telenti A, Heckenlively JR, Riazuddin SA, Frazer KA, Sieving PA, Ayyagari R. Chekuri A, et al. Among authors: guru aa. Hum Genet. 2018 Jul;137(6-7):447-458. doi: 10.1007/s00439-018-1897-9. Epub 2018 Jul 5. Hum Genet. 2018. PMID: 29978320 Free PMC article.
Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing.
Branham K, Matsui H, Biswas P, Guru AA, Hicks M, Suk JJ, Li H, Jakubosky D, Long T, Telenti A, Nariai N, Heckenlively JR, Frazer KA, Sieving PA, Ayyagari R. Branham K, et al. Among authors: guru aa. Physiol Genomics. 2016 Dec 1;48(12):922-927. doi: 10.1152/physiolgenomics.00101.2016. Epub 2016 Oct 7. Physiol Genomics. 2016. PMID: 27764769 Free PMC article.
Thoracic actinomycosis.
Bhardwaj G, Khan IA, Iqbal K, Guru AA. Bhardwaj G, et al. Among authors: guru aa. Indian Pediatr. 1986 Jan;23(1):69-70. Indian Pediatr. 1986. PMID: 3721575 No abstract available.
Urolithiasis in Kashmir.
Wani NA, Garyali RK, Guru AA, Bhan BL, Bhan B. Wani NA, et al. Among authors: guru aa. Int Surg. 1976 Sep;61(9):498-9. Int Surg. 1976. PMID: 965193 No abstract available.
12 results