1. Cloning of hok gene into anhydrotetracycline inducible pASK75 vector reveals potent antimicrobial effect of 19 amino acid long N‐terminal fragment of hok peptide. (23rd October 2020) Authors: Kaur, Anit; Muthukumarappa, Thungapathra; Kanta, Poonam; Banday, Aaqib Zaffar; Chidananda, Mohana Kumari Journal: Microbiology and immunology Issue: Volume 64:Number 11(2020) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Congenital Nephrotic Syndrome and the Heart: Lest We Forget!. Issue 3 (September 2021) Authors: Bhattacharya, Deepanjan; Kaur, Anit; Dawman, Lesa; Tiewsoh, Karalanglin Journal: Journal of neonatology Issue: Volume 35:Issue 3(2021) Page Start: 169 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cutaneous IgA vasculitis—presenting manifestation of a novel mutation in the IKZF1 gene. (24th October 2020) Authors: Banday, Aaqib Zaffar; Jindal, Ankur Kumar; Kaur, Anit; Saka, Ruchi; Parwaiz, Amber; Sachdeva, Man Updesh Singh; Rawat, Amit Journal: Rheumatology Issue: Volume 60:Number 3(2021) Page Start: e101 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Epstein‐Barr virus‐associated lymphocytic cholangitis in a child with X‐linked lymphoproliferative syndrome. (23rd September 2020) Authors: Bhattarai, Dharmagat; Vignesh, Pandiarajan; Kaur, Anit; Kumari, Poonam; V Menon, Jagadeesh; Geethanjali, Gude; Rawat, Amit Journal: Scandinavian journal of immunology Issue: Volume 93:Number 2(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Negative pressure flash pulmonary edema in a child with hereditary angioedema. Issue 7 (3rd July 2022) Authors: Barman, Prabal; Basu, Suprit; Thakur, Ishita; Chawla, Sanchi; Kaur, Anit; Jafra, Anudeep; Jindal, Ankur Kumar; Singh, Surjit Journal: Pediatric allergy and immunology Issue: Volume 33:Issue 7(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India. Issue 3 (5th December 2020) Authors: Jindal, Ankur K.; Rawat, Amit; Kaur, Anit; Sharma, Dhrubajyoti; Suri, Deepti; Gupta, Anju; Garg, Ravinder; Dogra, Sunil; Saikia, Biman; Minz, Ranjana W.; Singh, Surjit Editors: Atanaskovic‐Markovic, Marina Journal: Pediatric allergy and immunology Issue: Volume 32:Issue 3(2021) Page Start: 599 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Rare chromosomal aberrations detected in children with multiple congenital anomalies: utility of multiple ligation dependant probe amplification for developing countries. Issue 3 (12th April 2021) Authors: Pulipaka, Shirisha; Kaur, Anit; Bhatia, Prateek; Panigrahi, Inusha; Kaur, Anupriya Journal: Clinical dysmorphology Issue: Volume 30:Issue 3(2021) Page Start: 125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Rare chromosomal aberrations detected in children with multiple congenital anomalies: utility of multiple ligation dependant probe amplification for developing countries. Issue 3 (July 2021) Authors: Pulipaka, Shirisha; Kaur, Anit; Bhatia, Prateek; Panigrahi, Inusha; Kaur, Anupriya Journal: Clinical dysmorphology Issue: Volume 30:Issue 3(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Splice-site mutation in COPA gene and familial arthritis – a new frontier. (10th August 2020) Authors: Banday, Aaqib Zaffar; Kaur, Anit; Jindal, Ankur Kumar; Patra, Pratap Kumar; Guleria, Sandesh; Rawat, Amit Journal: Rheumatology Issue: Volume 60:Number 1(2021) Page Start: e7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Wolf–Hirschhorn syndrome: A case series from India. Issue 12 (10th September 2020) Authors: Chaudhry, Chakshu; Kaur, Anit; Panigrahi, Inusha; Kaur, Anupriya Journal: American journal of medical genetics Issue: Volume 182:Issue 12(2020) Page Start: 3048 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗