Zariwala MA - Search Results

1

Recessively Inherited Deficiency of Secreted WFDC2 (HE4) Causes Nasal Polyposis and Bronchiectasis.

Dougherty GW, Ostrowski LE, Nöthe-Menchen T, Raidt J, Schramm A, Olbrich H, Yin W, Sears PR, Dang H, Smith AJ, Beule AG, Hjeij R, Rutjes N, Haarman EG, Maas SM, Ferkol TW, Noone PG, Olivier KN, Bracht DC, Barbry P, Zaragosi LE, Fierville M, Kliesch S, Wohlgemuth K, König J, George S, Loges NT, Ceppe A, Markovetz MR, Luo H, Guo T, Rizk H, Eldesoky T, Dahlke K, Boldt K, Ueffing M, Hill DB, Pang YP, Knowles MR, Zariwala MA, Omran H. Dougherty GW, et al. Among authors: zariwala ma. Am J Respir Crit Care Med. 2024 Apr 16. doi: 10.1164/rccm.202308-1370OC. Online ahead of print. Am J Respir Crit Care Med. 2024. PMID: 38626355

2

p53 mutations in oropharyngeal carcinomas: a comparison of solitary and multiple primary tumours and lymph node metastases.

Zariwala M, Schmid S, Pfaltz M, Ohgaki H, Kleihues P, Schäfer R. Zariwala M, et al. Verh Dtsch Ges Pathol. 1994;78:252-4. Verh Dtsch Ges Pathol. 1994. PMID: 7533994

3

p53 gene mutations in oropharyngeal carcinomas: a comparison of solitary and multiple primary tumours and lymph-node metastases.

Zariwala M, Schmid S, Pfaltz M, Ohgaki H, Kleihues P, Schäfer R. Zariwala M, et al. Int J Cancer. 1994 Mar 15;56(6):807-11. doi: 10.1002/ijc.2910560608. Int J Cancer. 1994. PMID: 8119770

4

Mutations in the p16INK4/MTS1/CDKN2, p15INK4B/MTS2, and p18 genes in primary and metastatic lung cancer.

Okamoto A, Hussain SP, Hagiwara K, Spillare EA, Rusin MR, Demetrick DJ, Serrano M, Hannon GJ, Shiseki M, Zariwala M, et al. Okamoto A, et al. Cancer Res. 1995 Apr 1;55(7):1448-51. Cancer Res. 1995. PMID: 7882351

5

Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia.

Zariwala M, Noone PG, Sannuti A, Minnix S, Zhou Z, Leigh MW, Hazucha M, Carson JL, Knowles MR. Zariwala M, et al. Am J Respir Cell Mol Biol. 2001 Nov;25(5):577-83. doi: 10.1165/ajrcmb.25.5.4619. Am J Respir Cell Mol Biol. 2001. PMID: 11713099

6

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.

Olbrich H, Häffner K, Kispert A, Völkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H. Olbrich H, et al. Nat Genet. 2002 Feb;30(2):143-4. doi: 10.1038/ng817. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788826

7

Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia.

Noone PG, Zariwala M, Sannuti A, Minnix S, Leigh MW, Carson J, Knowles MR. Noone PG, et al. Chest. 2002 Mar;121(3 Suppl):97S. Chest. 2002. PMID: 11893720 No abstract available.

8

Investigation of the possible role of a novel gene, DPCD, in primary ciliary dyskinesia.

Zariwala M, O'Neal WK, Noone PG, Leigh MW, Knowles MR, Ostrowski LE. Zariwala M, et al. Am J Respir Cell Mol Biol. 2004 Apr;30(4):428-34. doi: 10.1165/rcmb.2003-0338RC. Epub 2003 Nov 20. Am J Respir Cell Mol Biol. 2004. PMID: 14630615

9

Primary ciliary dyskinesia: diagnostic and phenotypic features.

Noone PG, Leigh MW, Sannuti A, Minnix SL, Carson JL, Hazucha M, Zariwala MA, Knowles MR. Noone PG, et al. Among authors: zariwala ma. Am J Respir Crit Care Med. 2004 Feb 15;169(4):459-67. doi: 10.1164/rccm.200303-365OC. Epub 2003 Dec 4. Am J Respir Crit Care Med. 2004. PMID: 14656747

10

Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia.

Fliegauf M, Olbrich H, Horvath J, Wildhaber JH, Zariwala MA, Kennedy M, Knowles MR, Omran H. Fliegauf M, et al. Among authors: zariwala ma. Am J Respir Crit Care Med. 2005 Jun 15;171(12):1343-9. doi: 10.1164/rccm.200411-1583OC. Epub 2005 Mar 4. Am J Respir Crit Care Med. 2005. PMID: 15750039 Free PMC article.

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