Views

CrossRef citations to date

Altmetric

Articles

Mutations in exons 3 and 7 resulting in truncated expression of human ATP6V1B1 gene showing structural variations contributing to poor substrate binding-causative reason for distal renal tubular acidosis with sensorineural deafness

Pasupuleti Santhosh Kumar Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Katari Venkatesh Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Gopal Sowjenya Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Lokanathan Srikanth Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Manne Mudhu Sunitha Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Uppu Venkateswara Prasad Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Vimjam Swarupa Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

Sthanikam Yeswanth Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

P. Sri Ram Naveen Department of Nephrology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

A. Sridhar Department of Nephrology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

V. Siva Kumar Department of Nephrology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, India

P.V.G.K. Sarma Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences , Tirupati, AP517507, IndiaCorrespondence[email protected]

show all

Citations (7)

Keep up to date with the latest research on this topic with citation updates for this article.

Articles from other publishers (7)

Pasupuleti Santhosh Kumar, Lokanathan Srikanth, K. Sudheer Reddy & Potukuchi Venkata Gurunadha Krishna Sarma. (2020) Novel mutations in the RING-finger domain of BRCA1 gene in clinically diagnosed breast cancer patients. 3 Biotech 10:2.
Crossref

Chodimella Chandrasekhar, Pasupuleti Santhosh Kumar & Potukuchi Venkata Gurunadha Krishna Sarma. (2019) Novel mutations in the kinase domain of BCR-ABL gene causing imatinib resistance in chronic myeloid leukemia patients. Scientific Reports 9:1.
Crossref

Xiangzhong Zhao, Jingru Lu, Yanxia Gao, Xiaoling Wang, Yanhua Lang & Leping Shao. (2018) Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report. BMC Nephrology 19:1.
Crossref

Osamu Ichii, Teppei Nakamura, Taro Horino, Akira Yabuki, Yaser H.A. Elewa & Yasuhiro Kon. (2018) Abnormal Morphology of Distal Tubular Epithelial Cells Is Regulated by Genetic Factors Derived from Mouse Chromosome 12. The American Journal of Pathology 188:9, pages 2120-2138.
Crossref

Bodapati Chandra Mouleshwara Prasad, Vemula Venkata Ramesh Chandra, Agarwal Sudarsan, Pasupuleti Santhosh Kumar & Potukuchi Venkata Gurunadha Krishna Sarma. (2018) Clinical characteristics and NF1 gene mutation analysis of three successive generations in three different Indian families with neurofibromatosis type 1 and peripheral nerve sheath tumours. Journal of Clinical Neuroscience 53, pages 62-68.
Crossref

Pallipamu Prakash Babu, Pasupuleti Santhosh Kumar, Alladi Mohan, Bhattaram Siddhartha Kumar & Potukuchi Venkata Gurunadha Krishna Sarma. (2017) Novel mutations in the exon 5, intron 2 and 3′ UTR regions of IL-12B gene were observed in clinically proven tuberculosis patients of south India. Cytokine 99, pages 50-58.
Crossref

Bhattaram Siddhartha Kumar, Pasupuleti Santhosh Kumar, Nannepaga Sowgandhi, Bhattaram Manoj Prajwal, Alladi Mohan, Kadainti Venkata Subbaraya Sarma & Potukuchi Venkata Gurunadha Krishna Sarma. (2016) Identification of novel mutations in CD2BP1 gene in clinically proven rheumatoid arthritis patients of south India. European Journal of Medical Genetics 59:8, pages 404-412.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Mutations in exons 3 and 7 resulting in truncated expression of human ATP6V1B1 gene showing structural variations contributing to poor substrate binding-causative reason for distal renal tubular acidosis with sensorineural deafness

Articles from other publishers (7)

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

Mutations in exons 3 and 7 resulting in truncated expression of human ATP6V1B1 gene showing structural variations contributing to poor substrate binding-causative reason for distal renal tubular acidosis with sensorineural deafness

Citations (7)

Articles from other publishers (7)

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date